39 results on '"Nestler EJ"'
Search Results
2. Dynamic processing of hunger and thirst by common mesolimbic neural ensembles.
- Author
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Tan B, Nöbauer T, Browne CJ, Nestler EJ, Vaziri A, and Friedman JM
- Subjects
- Animals, Calcium metabolism, Mice, Nucleus Accumbens physiology, Reward, Water metabolism, Hunger, Thirst
- Abstract
The nucleus accumbens (NAc) is a canonical reward center that regulates feeding and drinking but it is not known whether these behaviors are mediated by same or different neurons. We employed two-photon calcium imaging in awake, behaving mice and found that during the appetitive phase, both hunger and thirst are sensed by a nearly identical population of individual D1 and D2 neurons in the NAc that respond monophasically to food cues in fasted animals and water cues in dehydrated animals. During the consummatory phase, we identified three distinct neuronal clusters that are temporally correlated with action initiation, consumption, and cessation shared by feeding and drinking. These dynamic clusters also show a nearly complete overlap of individual D1 neurons and extensive overlap among D2 neurons. Modulating D1 and D2 neural activities revealed analogous effects on feeding versus drinking behaviors. In aggregate, these data show that a highly overlapping set of D1 and D2 neurons in NAc detect food and water reward and elicit concordant responses to hunger and thirst. These studies establish a general role of this mesolimbic pathway in mediating instinctive behaviors by controlling motivation-associated variables rather than conferring behavioral specificity.
- Published
- 2022
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3. Nucleus accumbens feedforward inhibition circuit promotes cocaine self-administration.
- Author
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Yu J, Yan Y, Li KL, Wang Y, Huang YH, Urban NN, Nestler EJ, Schlüter OM, and Dong Y
- Subjects
- Animals, Basolateral Nuclear Complex, Female, Gene Knock-In Techniques, Long-Term Synaptic Depression, Male, Mice, Inbred C57BL, Neurons cytology, Receptor, Cannabinoid, CB1 physiology, Self Administration, Action Potentials physiology, Cocaine administration & dosage, Drug-Seeking Behavior physiology, Neural Inhibition, Neurons physiology, Nucleus Accumbens physiology, Vasoconstrictor Agents administration & dosage
- Abstract
The basolateral amygdala (BLA) sends excitatory projections to the nucleus accumbens (NAc) and regulates motivated behaviors partially by activating NAc medium spiny neurons (MSNs). Here, we characterized a feedforward inhibition circuit, through which BLA-evoked activation of NAc shell (NAcSh) MSNs was fine-tuned by GABAergic monosynaptic innervation from adjacent fast-spiking interneurons (FSIs). Specifically, BLA-to-NAcSh projections predominantly innervated NAcSh FSIs compared with MSNs and triggered action potentials in FSIs preceding BLA-mediated activation of MSNs. Due to these anatomical and temporal properties, activation of the BLA-to-NAcSh projection resulted in a rapid FSI-mediated inhibition of MSNs, timing-contingently dictating BLA-evoked activation of MSNs. Cocaine self-administration selectively and persistently up-regulated the presynaptic release probability of BLA-to-FSI synapses, entailing enhanced FSI-mediated feedforward inhibition of MSNs upon BLA activation. Experimentally enhancing the BLA-to-FSI transmission in vivo expedited the acquisition of cocaine self-administration. These results reveal a previously unidentified role of an FSI-embedded circuit in regulating NAc-based drug seeking and taking., Competing Interests: The authors declare no conflict of interest.
- Published
- 2017
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4. BDNF-TrkB controls cocaine-induced dendritic spines in rodent nucleus accumbens dissociated from increases in addictive behaviors.
- Author
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Anderson EM, Wissman AM, Chemplanikal J, Buzin N, Guzman D, Larson EB, Neve RL, Nestler EJ, Cowan CW, and Self DW
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- Animals, Anthralin, HEK293 Cells, Humans, Male, Neurons physiology, Nucleus Accumbens cytology, Rats, Rats, Sprague-Dawley, Receptor, trkB genetics, Signal Transduction, Brain-Derived Neurotrophic Factor metabolism, Cocaine pharmacology, Cocaine-Related Disorders, Dendritic Spines drug effects, Nucleus Accumbens physiology, Receptor, trkB metabolism
- Abstract
Chronic cocaine use is associated with prominent morphological changes in nucleus accumbens shell (NACsh) neurons, including increases in dendritic spine density along with enhanced motivation for cocaine, but a functional relationship between these morphological and behavioral phenomena has not been shown. Here we show that brain-derived neurotrophic factor (BDNF) signaling through tyrosine kinase B (TrkB) receptors in NACsh neurons is necessary for cocaine-induced dendritic spine formation by using either localized TrkB knockout or viral-mediated expression of a dominant negative, kinase-dead TrkB mutant. Interestingly, augmenting wild-type TrkB expression after chronic cocaine self-administration reverses the sustained increase in dendritic spine density, an effect mediated by TrkB signaling pathways that converge on extracellular regulated kinase. Loss of TrkB function after cocaine self-administration, however, leaves spine density intact but markedly enhances the motivation for cocaine, an effect mediated by specific loss of TrkB signaling through phospholipase Cgamma1 (PLCγ1). Conversely, overexpression of PLCγ1 both reduces the motivation for cocaine and reverses dendritic spine density, suggesting a potential target for the treatment of addiction in chronic users. Together, these findings indicate that BDNF-TrkB signaling both mediates and reverses cocaine-induced increases in dendritic spine density in NACsh neurons, and these morphological changes are entirely dissociable from changes in addictive behavior., Competing Interests: The authors declare no conflict of interest.
- Published
- 2017
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5. WAVE1 in neurons expressing the D1 dopamine receptor regulates cellular and behavioral actions of cocaine.
- Author
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Ceglia I, Lee KW, Cahill ME, Graves SM, Dietz D, Surmeier DJ, Nestler EJ, Nairn AC, Greengard P, and Kim Y
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- Animals, Dopamine Uptake Inhibitors pharmacology, Electrophysiological Phenomena genetics, Excitatory Postsynaptic Potentials genetics, Excitatory Postsynaptic Potentials physiology, Mice, Knockout, Mice, Transgenic, Motor Activity drug effects, Motor Activity genetics, Nucleus Accumbens metabolism, Nucleus Accumbens physiology, Phosphorylation drug effects, Receptors, Dopamine D1 genetics, Receptors, N-Methyl-D-Aspartate metabolism, Wiskott-Aldrich Syndrome Protein Family genetics, Cocaine pharmacology, Neurons metabolism, Receptors, Dopamine D1 metabolism, Spatial Behavior drug effects, Wiskott-Aldrich Syndrome Protein Family metabolism
- Abstract
Wiskott-Aldrich syndrome protein (WASP) family verprolin homologous protein 1 (WAVE1) regulates actin-related protein 2/3 (Arp2/3) complex-mediated actin polymerization. Our previous studies have found WAVE1 to be inhibited by Cdk5-mediated phosphorylation in brain and to play a role in the regulation of dendritic spine morphology. Here we report that mice in which WAVE1 was knocked out (KO) in neurons expressing the D1 dopamine receptor (D1-KO), but not mice where WAVE1 was knocked out in neurons expressing the D2 dopamine receptor (D2-KO), exhibited a significant decrease in place preference associated with cocaine. In contrast to wild-type (WT) and WAVE1 D2-KO mice, cocaine-induced sensitized locomotor behavior was not maintained in WAVE1 D1-KO mice. After chronic cocaine administration and following withdrawal, an acute cocaine challenge induced WAVE1 activation in striatum, which was assessed by dephosphorylation. The cocaine-induced WAVE1 dephosphorylation was attenuated by coadministration of either a D1 dopamine receptor or NMDA glutamate receptor antagonist. Upon an acute challenge of cocaine following chronic cocaine exposure and withdrawal, we also observed in WT, but not in WAVE1 D1-KO mice, a decrease in dendritic spine density and a decrease in the frequency of excitatory postsynaptic AMPA receptor currents in medium spiny projection neurons expressing the D1 dopamine receptor (D1-MSNs) in the nucleus accumbens. These results suggest that WAVE1 is involved selectively in D1-MSNs in cocaine-evoked neuronal activity-mediated feedback regulation of glutamatergic synapses., Competing Interests: The authors declare no conflict of interest.
- Published
- 2017
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6. Aberrant H3.3 dynamics in NAc promote vulnerability to depressive-like behavior.
- Author
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Lepack AE, Bagot RC, Peña CJ, Loh YE, Farrelly LA, Lu Y, Powell SK, Lorsch ZS, Issler O, Cates HM, Tamminga CA, Molina H, Shen L, Nestler EJ, Allis CD, and Maze I
- Subjects
- Adult, Aged, Animals, Depressive Disorder genetics, Depressive Disorder metabolism, Female, Gene Expression Regulation, Gene Knockdown Techniques, Histones genetics, Humans, Male, Mice, Mice, Inbred C57BL, Middle Aged, Nucleus Accumbens metabolism, Protein Isoforms genetics, Protein Isoforms metabolism, Stress, Psychological genetics, Depressive Disorder physiopathology, Histones metabolism, Nucleus Accumbens physiopathology, Stress, Psychological physiopathology
- Abstract
Human major depressive disorder (MDD), along with related mood disorders, is among the world's greatest public health concerns; however, its pathophysiology remains poorly understood. Persistent changes in gene expression are known to promote physiological aberrations implicated in MDD. More recently, histone mechanisms affecting cell type- and regional-specific chromatin structures have also been shown to contribute to transcriptional programs related to depressive behaviors, as well as responses to antidepressants. Although much emphasis has been placed in recent years on roles for histone posttranslational modifications and chromatin-remodeling events in the etiology of MDD, it has become increasingly clear that replication-independent histone variants (e.g., H3.3), which differ in primary amino acid sequence from their canonical counterparts, similarly play critical roles in the regulation of activity-dependent neuronal transcription, synaptic connectivity, and behavioral plasticity. Here, we demonstrate a role for increased H3.3 dynamics in the nucleus accumbens (NAc)-a key limbic brain reward region-in the regulation of aberrant social stress-mediated gene expression and the precipitation of depressive-like behaviors in mice. We find that molecular blockade of these dynamics promotes resilience to chronic social stress and results in a partial renormalization of stress-associated transcriptional patterns in the NAc. In sum, our findings establish H3.3 dynamics as a critical, and previously undocumented, regulator of mood and suggest that future therapies aimed at modulating striatal histone dynamics may potentiate beneficial behavioral adaptations to negative emotional stimuli., Competing Interests: The authors declare no conflict of interest.
- Published
- 2016
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7. Histone arginine methylation in cocaine action in the nucleus accumbens.
- Author
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Damez-Werno DM, Sun H, Scobie KN, Shao N, Rabkin J, Dias C, Calipari ES, Maze I, Pena CJ, Walker DM, Cahill ME, Chandra R, Gancarz A, Mouzon E, Landry JA, Cates H, Lobo MK, Dietz D, Allis CD, Guccione E, Turecki G, Defilippi P, Neve RL, Hurd YL, Shen L, and Nestler EJ
- Subjects
- Acetylation, Animals, Carrier Proteins metabolism, Cocaine-Related Disorders genetics, Cocaine-Related Disorders pathology, Histones genetics, Humans, Male, Methylation, Mice, Mice, Inbred C57BL, Neurons metabolism, Neurons pathology, Nucleus Accumbens pathology, Protein-Arginine N-Methyltransferases genetics, Protein-Arginine N-Methyltransferases metabolism, Rats, Rats, Sprague-Dawley, Receptors, Dopamine D1 genetics, Receptors, Dopamine D1 metabolism, Receptors, Dopamine D2 genetics, Receptors, Dopamine D2 metabolism, Carrier Proteins genetics, Cocaine administration & dosage, Cocaine-Related Disorders metabolism, Histones metabolism, Nucleus Accumbens metabolism, Protein Processing, Post-Translational
- Abstract
Repeated cocaine exposure regulates transcriptional regulation within the nucleus accumbens (NAc), and epigenetic mechanisms-such as histone acetylation and methylation on Lys residues-have been linked to these lasting actions of cocaine. In contrast to Lys methylation, the role of histone Arg (R) methylation remains underexplored in addiction models. Here we show that protein-R-methyltransferase-6 (PRMT6) and its associated histone mark, asymmetric dimethylation of R2 on histone H3 (H3R2me2a), are decreased in the NAc of mice and rats after repeated cocaine exposure, including self-administration, and in the NAc of cocaine-addicted humans. Such PRMT6 down-regulation occurs selectively in NAc medium spiny neurons (MSNs) expressing dopamine D2 receptors (D2-MSNs), with opposite regulation occurring in D1-MSNs, and serves to protect against cocaine-induced addictive-like behavioral abnormalities. Using ChIP-seq, we identified Src kinase signaling inhibitor 1 (Srcin1; also referred to as p140Cap) as a key gene target for reduced H3R2me2a binding, and found that consequent Srcin1 induction in the NAc decreases Src signaling, cocaine reward, and the motivation to self-administer cocaine. Taken together, these findings suggest that suppression of Src signaling in NAc D2-MSNs, via PRMT6 and H3R2me2a down-regulation, functions as a homeostatic brake to restrain cocaine action, and provide novel candidates for the development of treatments for cocaine addiction., Competing Interests: The authors declare no conflict of interest.
- Published
- 2016
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8. Re-silencing of silent synapses unmasks anti-relapse effects of environmental enrichment.
- Author
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Ma YY, Wang X, Huang Y, Marie H, Nestler EJ, Schlüter OM, and Dong Y
- Subjects
- Amygdala physiopathology, Animals, Cocaine adverse effects, Male, Neural Inhibition, Neural Pathways physiopathology, Rats, Rats, Sprague-Dawley, Recurrence, Treatment Outcome, Behavior Therapy methods, Cocaine-Related Disorders etiology, Cocaine-Related Disorders therapy, Nucleus Accumbens physiopathology, Substance Withdrawal Syndrome physiopathology, Synapses
- Abstract
Environmental enrichment (EE) has long been postulated as a behavioral treatment for drug addiction based on its preventive effects in animal models: rodents experiencing prior EE exhibit increased resistance to establishing drug taking and seeking. However, the therapeutic effects of EE, namely, the effects of EE when applied after drug exposure, are often marginal and transient. Using incubation of cue-induced cocaine craving, a rat relapse model depicting progressive intensification of cocaine seeking after withdrawal from cocaine self-administration, our present study reveals that after cocaine withdrawal, in vivo circuit-specific long-term depression (LTD) unmasks the therapeutic power of EE to achieve long-lasting anti-relapse effects. Specifically, our previous results show that cocaine self-administration generates AMPA receptor (AMPAR)-silent excitatory synapses within the basolateral amygdala (BLA) to nucleus accumbens (NAc) projection, and maturation of these silent synapses via recruiting calcium-permeable (CP) AMPARs contributes to incubation of cocaine craving. Here, we show that after cocaine withdrawal and maturation of silent synapses, the BLA-to-NAc projection became highly resistant to EE. However, optogenetic LTD applied to this projection in vivo transiently re-silenced these silent synapses by removing CP-AMPARs. During this transient window, application of EE resulted in the insertion of nonCP-AMPARs, thereby remodeling the "incubated" BLA-to-NAc projection. Consequently, incubation of cocaine craving was decreased persistently. These results reveal a mechanistic basis through which the persistent anti-relapse effects of EE can be unleashed after drug withdrawal.
- Published
- 2016
- Full Text
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9. In vivo imaging identifies temporal signature of D1 and D2 medium spiny neurons in cocaine reward.
- Author
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Calipari ES, Bagot RC, Purushothaman I, Davidson TJ, Yorgason JT, Peña CJ, Walker DM, Pirpinias ST, Guise KG, Ramakrishnan C, Deisseroth K, and Nestler EJ
- Subjects
- Analysis of Variance, Animals, Cocaine administration & dosage, Cues, Dopamine Uptake Inhibitors administration & dosage, Dopamine Uptake Inhibitors pharmacology, Drug-Seeking Behavior drug effects, Immunohistochemistry, Mice, Inbred C57BL, Mice, Transgenic, Neuroimaging methods, Neurons metabolism, Nucleus Accumbens cytology, Nucleus Accumbens metabolism, Receptors, Dopamine D1 genetics, Receptors, Dopamine D2 genetics, Signal Transduction drug effects, Cocaine pharmacology, Neurons drug effects, Receptors, Dopamine D1 metabolism, Receptors, Dopamine D2 metabolism, Reward
- Abstract
The reinforcing and rewarding properties of cocaine are attributed to its ability to increase dopaminergic transmission in nucleus accumbens (NAc). This action reinforces drug taking and seeking and leads to potent and long-lasting associations between the rewarding effects of the drug and the cues associated with its availability. The inability to extinguish these associations is a key factor contributing to relapse. Dopamine produces these effects by controlling the activity of two subpopulations of NAc medium spiny neurons (MSNs) that are defined by their predominant expression of either dopamine D1 or D2 receptors. Previous work has demonstrated that optogenetically stimulating D1 MSNs promotes reward, whereas stimulating D2 MSNs produces aversion. However, we still lack a clear understanding of how the endogenous activity of these cell types is affected by cocaine and encodes information that drives drug-associated behaviors. Using fiber photometry calcium imaging we define D1 MSNs as the specific population of cells in NAc that encodes information about drug associations and elucidate the temporal profile with which D1 activity is increased to drive drug seeking in response to contextual cues. Chronic cocaine exposure dysregulates these D1 signals to both prevent extinction and facilitate reinstatement of drug seeking to drive relapse. Directly manipulating these D1 signals using designer receptors exclusively activated by designer drugs prevents contextual associations. Together, these data elucidate the responses of D1- and D2-type MSNs in NAc to acute cocaine and during the formation of context-reward associations and define how prior cocaine exposure selectively dysregulates D1 signaling to drive relapse.
- Published
- 2016
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10. Essential role of poly(ADP-ribosyl)ation in cocaine action.
- Author
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Scobie KN, Damez-Werno D, Sun H, Shao N, Gancarz A, Panganiban CH, Dias C, Koo J, Caiafa P, Kaufman L, Neve RL, Dietz DM, Shen L, and Nestler EJ
- Subjects
- Animals, Behavior, Animal drug effects, Chromatin Immunoprecipitation, Cocaine administration & dosage, Dendritic Spines drug effects, Dendritic Spines metabolism, Gene Expression Regulation, Enzymologic drug effects, Genome genetics, Immunoglobulin G metabolism, Male, Membrane Proteins metabolism, Mice, Mice, Inbred C57BL, Nucleus Accumbens drug effects, Nucleus Accumbens enzymology, Poly(ADP-ribose) Polymerases genetics, Poly(ADP-ribose) Polymerases metabolism, Protein Binding drug effects, RNA, Messenger genetics, RNA, Messenger metabolism, Rats, Substrate Specificity drug effects, Transcription, Genetic drug effects, Cocaine pharmacology, Poly Adenosine Diphosphate Ribose metabolism
- Abstract
Many of the long-term effects of cocaine on the brain's reward circuitry have been shown to be mediated by alterations in gene expression. Several chromatin modifications, including histone acetylation and methylation, have been implicated in this regulation, but the effect of other histone modifications remains poorly understood. Poly(ADP-ribose) polymerase-1 (PARP-1), a ubiquitous and abundant nuclear protein, catalyzes the synthesis of a negatively charged polymer called poly(ADP-ribose) or PAR on histones and other substrate proteins and forms transcriptional regulatory complexes with several other chromatin proteins. Here, we identify an essential role for PARP-1 in cocaine-induced molecular, neural, and behavioral plasticity. Repeated cocaine administration, including self-administration, increased global levels of PARP-1 and its mark PAR in mouse nucleus accumbens (NAc), a key brain reward region. Using PARP-1 inhibitors and viral-mediated gene transfer, we established that PARP-1 induction in NAc mediates enhanced behavioral responses to cocaine, including increased self-administration of the drug. Using chromatin immunoprecipitation sequencing, we demonstrated a global, genome-wide enrichment of PARP-1 in NAc of cocaine-exposed mice and identified several PARP-1 target genes that could contribute to the lasting effects of cocaine. Specifically, we identified sidekick-1--important for synaptic connections during development--as a critical PARP-1 target gene involved in cocaine's behavioral effects as well as in its ability to induce dendritic spines on NAc neurons. These findings establish the involvement of PARP-1 and PARylation in the long-term actions of cocaine.
- Published
- 2014
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11. Regulator of G protein signaling 4 [corrected] is a crucial modulator of antidepressant drug action in depression and neuropathic pain models.
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Stratinaki M, Varidaki A, Mitsi V, Ghose S, Magida J, Dias C, Russo SJ, Vialou V, Caldarone BJ, Tamminga CA, Nestler EJ, and Zachariou V
- Subjects
- Adolescent, Adult, Aged, Aged, 80 and over, Animals, Behavior, Animal, Brain pathology, Desipramine pharmacology, Female, Humans, Male, Mice, Mice, Inbred C57BL, Mice, Knockout, Middle Aged, Mood Disorders drug therapy, Signal Transduction drug effects, Young Adult, Antidepressive Agents pharmacology, Depression drug therapy, GTP-Binding Proteins metabolism, Gene Expression Regulation, Neuralgia drug therapy, RGS Proteins metabolism
- Abstract
Regulator of G protein signaling 4 (Rgs4) is a signal transduction protein that controls the function of monoamine, opiate, muscarinic, and other G protein-coupled receptors via interactions with Gα subunits. Rgs4 is expressed in several brain regions involved in mood, movement, cognition, and addiction and is regulated by psychotropic drugs, stress, and corticosteroids. In this study, we use genetic mouse models and viral-mediated gene transfer to examine the role of Rgs4 in the actions of antidepressant medications. We first analyzed human postmortem brain tissue and found robust up-regulation of RGS4 expression in the nucleus accumbens (NAc) of subjects receiving standard antidepressant medications that target monoamine systems. Behavioral studies of mice lacking Rgs4, including specific knockdowns in NAc, demonstrate that Rgs4 in this brain region acts as a positive modulator of the antidepressant-like and antiallodynic-like actions of several monoamine-directed antidepressant drugs, including tricyclic antidepressants, selective serotonin reuptake inhibitors, and norepinephrine reuptake inhibitors. Studies using viral-mediated increases in Rgs4 activity in NAc further support this hypothesis. Interestingly, in prefrontal cortex, Rgs4 acts as a negative modulator of the actions of nonmonoamine-directed drugs that are purported to act as antidepressants: the N-methyl-D-aspartate glutamate receptor antagonist ketamine and the delta opioid agonist (+)-4-[(αR)-α-((2S,5R)-4-Allyl-2,5-dimethyl-1-piperazinyl)-3-methoxybenzyl]-N,N-diethylbenzamide. Together, these data reveal a unique modulatory role of Rgs4 in the brain region-specific actions of a wide range of antidepressant drugs and indicate that pharmacological interventions at the level of RGS4 activity may enhance the actions of such drugs used for the treatment of depression and neuropathic pain.
- Published
- 2013
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12. ∆FosB differentially modulates nucleus accumbens direct and indirect pathway function.
- Author
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Grueter BA, Robison AJ, Neve RL, Nestler EJ, and Malenka RC
- Subjects
- Animals, Cocaine pharmacology, Conditioning, Psychological drug effects, Dendritic Spines drug effects, Dendritic Spines metabolism, Dendritic Spines physiology, Dopamine Uptake Inhibitors pharmacology, Excitatory Postsynaptic Potentials drug effects, Excitatory Postsynaptic Potentials genetics, Excitatory Postsynaptic Potentials physiology, In Vitro Techniques, Luminescent Proteins genetics, Luminescent Proteins metabolism, Male, Mice, Mice, Inbred C57BL, Mice, Transgenic, Microscopy, Confocal, Motor Activity drug effects, Nucleus Accumbens cytology, Nucleus Accumbens metabolism, Patch-Clamp Techniques, Proto-Oncogene Proteins c-fos genetics, Receptors, Dopamine D1 genetics, Receptors, Dopamine D1 metabolism, Receptors, Dopamine D1 physiology, Receptors, Dopamine D2 genetics, Receptors, Dopamine D2 metabolism, Receptors, Dopamine D2 physiology, Sodium Channel Blockers pharmacology, Synapses drug effects, Synapses metabolism, Synaptic Transmission drug effects, Synaptic Transmission genetics, Tetrodotoxin pharmacology, Nucleus Accumbens physiology, Proto-Oncogene Proteins c-fos metabolism, Synapses physiology, Synaptic Transmission physiology
- Abstract
Synaptic modifications in nucleus accumbens (NAc) medium spiny neurons (MSNs) play a key role in adaptive and pathological reward-dependent learning, including maladaptive responses involved in drug addiction. NAc MSNs participate in two parallel circuits, direct and indirect pathways that subserve distinct behavioral functions. Modification of NAc MSN synapses may occur in part via changes in the transcriptional potential of certain genes in a cell type–specific manner. The transcription factor ∆FosB is one of the key proteins implicated in the gene expression changes in NAc caused by drugs of abuse, yet its effects on synaptic function in NAc MSNs are unknown. Here, we demonstrate that overexpression of ∆FosB decreased excitatory synaptic strength and likely increased silent synapses onto D1 dopamine receptor–expressing direct pathway MSNs in both the NAc shell and core. In contrast, ∆FosB likely decreased silent synapses onto NAc shell, but not core, D2 dopamine receptor–expressing indirect pathway MSNs. Analysis of NAc MSN dendritic spine morphology revealed that ∆FosB increased the density of immature spines in D1 direct but not D2 indirect pathway MSNs. To determine the behavioral consequences of cell type-specific actions of ∆FosB, we selectively overexpressed ∆FosB in D1 direct or D2 indirect MSNs in NAc in vivo and found that direct (but not indirect) pathway MSN expression enhances behavioral responses to cocaine. These results reveal that ∆FosB in NAc differentially modulates synaptic properties and reward-related behaviors in a cell type- and subregion-specific fashion.
- Published
- 2013
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13. Cocaine dynamically regulates heterochromatin and repetitive element unsilencing in nucleus accumbens.
- Author
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Maze I, Feng J, Wilkinson MB, Sun H, Shen L, and Nestler EJ
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- Analysis of Variance, Animals, Base Sequence, Blotting, Western, Chromatin Immunoprecipitation, DNA Primers genetics, Heterochromatin drug effects, Immunohistochemistry, Long Interspersed Nucleotide Elements genetics, Lysine metabolism, Methylation drug effects, Mice, Models, Statistical, Molecular Sequence Data, Nucleus Accumbens drug effects, Polymerase Chain Reaction, Reverse Transcriptase Polymerase Chain Reaction, Reward, Sequence Analysis, DNA, Cocaine toxicity, Cocaine-Related Disorders metabolism, Gene Regulatory Networks drug effects, Genomic Instability drug effects, Heterochromatin metabolism, Histones metabolism, Nucleus Accumbens metabolism
- Abstract
Repeated cocaine exposure induces persistent alterations in genome-wide transcriptional regulatory networks, chromatin remodeling activity and, ultimately, gene expression profiles in the brain's reward circuitry. Virtually all previous investigations have centered on drug-mediated effects occurring throughout active euchromatic regions of the genome, with very little known concerning the impact of cocaine exposure on the regulation and maintenance of heterochromatin in adult brain. Here, we report that cocaine dramatically and dynamically alters heterochromatic histone H3 lysine 9 trimethylation (H3K9me3) in the nucleus accumbens (NAc), a key brain reward region. Furthermore, we demonstrate that repeated cocaine exposure causes persistent decreases in heterochromatization in this brain region, suggesting a potential role for heterochromatic regulation in the long-term actions of cocaine. To identify precise genomic loci affected by these alterations, chromatin immunoprecipitation followed by massively parallel DNA sequencing (ChIP-Seq) was performed on NAc. ChIP-Seq analyses confirmed the existence of the H3K9me3 mark mainly within intergenic regions of the genome and identified specific patterns of cocaine-induced H3K9me3 regulation at repetitive genomic sequences. Cocaine-mediated decreases in H3K9me3 enrichment at specific genomic repeats [e.g., long interspersed nuclear element (LINE)-1 repeats] were further confirmed by the increased expression of LINE-1 retrotransposon-associated repetitive elements in NAc. Such increases likely reflect global patterns of genomic destabilization in this brain region after repeated cocaine administration and open the door for future investigations into the epigenetic and genetic basis of drug addiction.
- Published
- 2011
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14. Essential role of the cAMP-cAMP response-element binding protein pathway in opiate-induced homeostatic adaptations of locus coeruleus neurons.
- Author
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Cao JL, Vialou VF, Lobo MK, Robison AJ, Neve RL, Cooper DC, Nestler EJ, and Han MH
- Subjects
- Adaptation, Physiological drug effects, Adenylyl Cyclases genetics, Animals, Cells, Cultured, Cyclic AMP metabolism, Cyclic AMP Response Element-Binding Protein antagonists & inhibitors, Gene Knockout Techniques, Homeostasis drug effects, Locus Coeruleus metabolism, Locus Coeruleus physiology, Mice, Mice, Transgenic, Neurons metabolism, Neurons physiology, Rats, Rats, Sprague-Dawley, Cyclic AMP Response Element-Binding Protein metabolism, Locus Coeruleus drug effects, Morphine pharmacology, Neurons drug effects
- Abstract
Excessive inhibition of brain neurons in primary or slice cultures can induce homeostatic intrinsic plasticity, but the functional role and underlying molecular mechanisms of such plasticity are poorly understood. Here, we developed an ex vivo locus coeruleus (LC) slice culture system and successfully recapitulated the opiate-induced homeostatic adaptation in electrical activity of LC neurons seen in vivo. We investigated the mechanisms underlying this adaptation in LC slice cultures by use of viral-mediated gene transfer and genetic mutant mice. We found that short-term morphine treatment of slice cultures almost completely abolished the firing of LC neurons, whereas chronic morphine treatment increased LC neuronal excitability as revealed during withdrawal. This increased excitability was mediated by direct activation of opioid receptors and up-regulation of the cAMP pathway and accompanied by increased cAMP response-element binding protein (CREB) activity. Overexpression of a dominant negative CREB mutant blocked the increase in LC excitability induced by morphine- or cAMP-pathway activation. Knockdown of CREB in slice cultures from floxed CREB mice similarly decreased LC excitability. Furthermore, the ability of morphine or CREB overexpression to up-regulate LC firing was blocked by knockout of the CREB target adenylyl cyclase 8. Together, these findings provide direct evidence that prolonged exposure to morphine induces homeostatic plasticity intrinsic to LC neurons, involving up-regulation of the cAMP-CREB signaling pathway, which then enhances LC neuronal excitability.
- Published
- 2010
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15. Distinct subclasses of medium spiny neurons differentially regulate striatal motor behaviors.
- Author
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Bateup HS, Santini E, Shen W, Birnbaum S, Valjent E, Surmeier DJ, Fisone G, Nestler EJ, and Greengard P
- Subjects
- Animals, Catalepsy chemically induced, Catalepsy physiopathology, Cocaine pharmacology, Corpus Striatum cytology, Dopamine Agents toxicity, Dopamine Uptake Inhibitors pharmacology, Dopamine and cAMP-Regulated Phosphoprotein 32 genetics, Dopamine and cAMP-Regulated Phosphoprotein 32 metabolism, Dyskinesia, Drug-Induced etiology, Dyskinesia, Drug-Induced physiopathology, Female, Fluorescent Antibody Technique, Green Fluorescent Proteins genetics, Green Fluorescent Proteins metabolism, Haloperidol toxicity, Immunohistochemistry, Levodopa toxicity, Long-Term Potentiation physiology, Male, Mice, Mice, Inbred C57BL, Mice, Knockout, Mice, Transgenic, Motor Activity drug effects, Neuronal Plasticity physiology, Neurons classification, Neurons cytology, Synaptic Potentials physiology, Corpus Striatum metabolism, Dopamine and cAMP-Regulated Phosphoprotein 32 physiology, Motor Activity physiology, Neurons metabolism
- Abstract
The direct and indirect pathways of the basal ganglia have been proposed to oppositely regulate locomotion and differentially contribute to pathological behaviors. Analysis of the distinct contributions of each pathway to behavior has been a challenge, however, due to the difficulty of selectively investigating the neurons comprising the two pathways using conventional techniques. Here we present two mouse models in which the function of striatonigral or striatopallidal neurons is selectively disrupted due to cell type-specific deletion of the striatal signaling protein dopamine- and cAMP-regulated phosphoprotein Mr 32kDa (DARPP-32). Using these mice, we found that the loss of DARPP-32 in striatonigral neurons decreased basal and cocaine-induced locomotion and abolished dyskinetic behaviors in response to the Parkinson's disease drug L-DOPA. Conversely, the loss of DARPP-32 in striatopallidal neurons produced a robust increase in locomotor activity and a strongly reduced cataleptic response to the antipsychotic drug haloperidol. These findings provide insight into the selective contributions of the direct and indirect pathways to striatal motor behaviors.
- Published
- 2010
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16. Adult hippocampal neurogenesis is functionally important for stress-induced social avoidance.
- Author
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Lagace DC, Donovan MH, DeCarolis NA, Farnbauch LA, Malhotra S, Berton O, Nestler EJ, Krishnan V, and Eisch AJ
- Subjects
- Animals, Brain-Derived Neurotrophic Factor metabolism, Bromodeoxyuridine metabolism, Cell Death, Hippocampus metabolism, Male, Mice, S Phase, Signal Transduction, Avoidance Learning, Hippocampus pathology, Neurogenesis, Stress, Psychological pathology
- Abstract
The long-term response to chronic stress is variable, with some individuals developing maladaptive functioning, although other "resilient" individuals do not. Stress reduces neurogenesis in the dentate gyrus subgranular zone (SGZ), but it is unknown if stress-induced changes in neurogenesis contribute to individual vulnerability. Using a chronic social defeat stress model, we explored whether the susceptibility to stress-induced social avoidance was related to changes in SGZ proliferation and neurogenesis. Immediately after social defeat, stress-exposed mice (irrespective of whether they displayed social avoidance) had fewer proliferating SGZ cells labeled with the S-phase marker BrdU. The decrease was transient, because BrdU cell numbers were normalized 24 h later. The survival of BrdU cells labeled before defeat stress was also not altered. However, 4 weeks later, mice that displayed social avoidance had more surviving dentate gyrus neurons. Thus, dentate gyrus neurogenesis is increased after social defeat stress selectively in mice that display persistent social avoidance. Supporting a functional role for adult-generated dentate gyrus neurons, ablation of neurogenesis via cranial ray irradiation robustly inhibited social avoidance. These data show that the time window after cessation of stress is a critical period for the establishment of persistent cellular and behavioral responses to stress and that a compensatory enhancement in neurogenesis is related to the long-term individual differences in maladaptive responses to stress.
- Published
- 2010
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17. Nuclear factor-kappaB is a critical mediator of stress-impaired neurogenesis and depressive behavior.
- Author
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Koo JW, Russo SJ, Ferguson D, Nestler EJ, and Duman RS
- Subjects
- Animals, Cell Proliferation drug effects, Cells, Cultured, Depressive Disorder psychology, Female, Hippocampus cytology, Hippocampus metabolism, Interleukin-1beta pharmacology, Male, Mice, Mice, Transgenic, NF-kappa B antagonists & inhibitors, NF-kappa B genetics, Neurons cytology, Neurons drug effects, Neurons metabolism, Phenylenediamines pharmacology, Rats, Rats, Sprague-Dawley, Restraint, Physical psychology, Signal Transduction drug effects, Stem Cells cytology, Stem Cells drug effects, Stem Cells metabolism, Stress, Psychological physiopathology, Thiophenes pharmacology, Depressive Disorder physiopathology, NF-kappa B metabolism, Neurogenesis physiology, Signal Transduction physiology
- Abstract
Proinflammatory cytokines, such as IL-1beta, have been implicated in the cellular and behavioral effects of stress and in mood disorders, although the downstream signaling pathways underlying these effects have not been determined. In the present study, we demonstrate a critical role for NF-kappaB signaling in the actions of IL-1beta and stress. Stress inhibition of neurogenesis in the adult hippocampus, which has been implicated in the prodepressive effects of stress, is blocked by administration of an inhibitor of NF-kappaB. Further analysis reveals that stress activates NF-kappaB signaling and decreases proliferation of neural stem-like cells but not early neural progenitor cells in the adult hippocampus. We also find that depressive-like behaviors caused by exposure to chronic stress are mediated by NF-kappaB signaling. Together, these data identify NF-kappaB signaling as a critical mediator of the antineurogenic and behavioral actions of stress and suggest previously undescribed therapeutical targets for depression.
- Published
- 2010
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18. Nucleus accumbens dopamine mediates amphetamine-induced impairment of social bonding in a monogamous rodent species.
- Author
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Liu Y, Aragona BJ, Young KA, Dietz DM, Kabbaj M, Mazei-Robison M, Nestler EJ, and Wang Z
- Subjects
- Animals, Blotting, Western, Female, Male, Amphetamine pharmacology, Arvicolinae physiology, Dopamine metabolism, Nucleus Accumbens metabolism, Sexual Behavior, Animal drug effects, Social Behavior
- Abstract
The prairie vole (Microtus ochrogaster) is a socially monogamous rodent species that forms pair bonds after mating, a behavior in which central dopamine (DA) has been implicated. Here, we used male prairie voles to examine the effects of drug exposure on pair bonding and related neural circuitry. In our first experiment, amphetamine (AMPH) motivated behavior was examined using a conditioned place preference (CPP) paradigm and was shown to be mediated by activation of D1-like DA receptors. Next, we examined the effects of repeated AMPH exposure on pair bonding. Intact and saline pretreated control males displayed mating-induced partner preferences, whereas males pretreated with AMPH at the doses effective to induce CPP failed to show mating-induced partner preferences. Such AMPH treatment also enhanced D1, but not D2, DA receptor expression in the nucleus accumbens (NAcc). Furthermore, pharmacological blockade of D1-like DA receptors in the NAcc rescued mating-induced partner preferences in AMPH-treated males. Together, our data indicate that repeated AMPH exposure may narrow the behavioral repertoire of male prairie voles via a DA receptor-specific mechanism in the NAcc, resulting in the impairment of pair bond formation.
- Published
- 2010
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19. Mania-like behavior induced by disruption of CLOCK.
- Author
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Roybal K, Theobold D, Graham A, DiNieri JA, Russo SJ, Krishnan V, Chakravarty S, Peevey J, Oehrlein N, Birnbaum S, Vitaterna MH, Orsulak P, Takahashi JS, Nestler EJ, Carlezon WA Jr, and McClung CA
- Subjects
- Analysis of Variance, Animals, Behavioral Symptoms genetics, Bipolar Disorder drug therapy, Bipolar Disorder pathology, Bipolar Disorder therapy, CLOCK Proteins, Electric Stimulation, Gene Expression Regulation genetics, Gene Transfer Techniques, Genetic Therapy methods, Glycogen Synthase Kinase 3 genetics, Glycogen Synthase Kinase 3 beta, Immunohistochemistry, Lithium pharmacology, Lithium therapeutic use, Lithium Compounds pharmacology, Lithium Compounds therapeutic use, Locomotion drug effects, Mice, Mutagenesis, Mutation genetics, Trans-Activators therapeutic use, Ventral Tegmental Area drug effects, Bipolar Disorder genetics, Circadian Rhythm genetics, Trans-Activators genetics
- Abstract
Circadian rhythms and the genes that make up the molecular clock have long been implicated in bipolar disorder. Genetic evidence in bipolar patients suggests that the central transcriptional activator of molecular rhythms, CLOCK, may be particularly important. However, the exact role of this gene in the development of this disorder remains unclear. Here we show that mice carrying a mutation in the Clock gene display an overall behavioral profile that is strikingly similar to human mania, including hyperactivity, decreased sleep, lowered depression-like behavior, lower anxiety, and an increase in the reward value for cocaine, sucrose, and medial forebrain bundle stimulation. Chronic administration of the mood stabilizer lithium returns many of these behavioral responses to wild-type levels. In addition, the Clock mutant mice have an increase in dopaminergic activity in the ventral tegmental area, and their behavioral abnormalities are rescued by expressing a functional CLOCK protein via viral-mediated gene transfer specifically in the ventral tegmental area. These findings establish the Clock mutant mice as a previously unrecognized model of human mania and reveal an important role for CLOCK in the dopaminergic system in regulating behavior and mood.
- Published
- 2007
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20. Inhibition of Cdk5 in the nucleus accumbens enhances the locomotor-activating and incentive-motivational effects of cocaine.
- Author
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Taylor JR, Lynch WJ, Sanchez H, Olausson P, Nestler EJ, and Bibb JA
- Subjects
- Animals, Cocaine metabolism, Conditioning, Operant, Cyclin-Dependent Kinase 5 antagonists & inhibitors, Dopamine metabolism, Dopamine Uptake Inhibitors pharmacology, Male, Purines pharmacology, Rats, Rats, Sprague-Dawley, Reinforcement, Psychology, Roscovitine, Signal Transduction, Cocaine pharmacology, Cyclin-Dependent Kinase 5 physiology, Enzyme Inhibitors pharmacology, Kinetin pharmacology, Nucleus Accumbens drug effects, Nucleus Accumbens metabolism
- Abstract
Neuronal adaptations in striatal dopamine signaling have been implicated in enhanced responses to addictive drugs. Cyclin-dependent kinase 5 (Cdk5) regulates striatal dopamine signaling and is a downstream target gene of the transcription factor DeltaFosB, which accumulates in striatal neurons after chronic cocaine exposure. Here we investigated the role of Cdk5 activity in the nucleus accumbens (NAc) on cocaine-induced locomotor sensitization, responding for reward-associated stimuli (conditioned reinforcement), and cocaine self-administration under a progressive ratio schedule. Repeated infusions of the Cdk5 inhibitor roscovitine into the NAc before cocaine injections augmented both the development and expression of cocaine sensitization without having any intrinsic stimulant actions of its own. Additionally, repeated intra-NAc infusions of roscovitine to saline-injected rats enhanced locomotor responses to a subsequent cocaine challenge. Similar effects were found after infusions of another Cdk5 inhibitor, olomoucine, but not its inactive congener, iso-olomoucine. Repeated inhibition of Cdk5 within the NAc also robustly enhanced the incentive-motivational effects of cocaine, similar to the effect of prior repeated cocaine exposure. The enhanced responding with conditioned reinforcement induced by cocaine persisted at least 2 weeks after the final roscovitine infusion. NAc infusions of olomoucine also produced acute and enduring increases in "breakpoints" achieved on a progressive ratio schedule for cocaine reinforcement. These results demonstrate profound and persistent effects of NAc Cdk5 inhibition on locomotor sensitization and incentive-motivational processes and provide direct evidence for a role for striatal Cdk5-induced alterations in the brain's long-term adaptations to cocaine.
- Published
- 2007
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21. Adenylyl cyclase type 5 (AC5) is an essential mediator of morphine action.
- Author
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Kim KS, Lee KW, Lee KW, Im JY, Yoo JY, Kim SW, Lee JK, Nestler EJ, and Han PL
- Subjects
- Adenylyl Cyclases deficiency, Adenylyl Cyclases genetics, Animals, Behavior, Animal drug effects, Behavior, Animal physiology, Conditioning, Psychological drug effects, Corpus Striatum drug effects, Corpus Striatum enzymology, Isoenzymes deficiency, Isoenzymes genetics, Mice, Mice, Inbred C57BL, Mice, Knockout, Motor Activity drug effects, Pain Measurement, Receptors, Opioid agonists, Receptors, Opioid physiology, Receptors, Opioid, delta drug effects, Receptors, Opioid, delta physiology, Receptors, Opioid, mu drug effects, Receptors, Opioid, mu physiology, Signal Transduction, Substance Withdrawal Syndrome, Adenylyl Cyclases metabolism, Isoenzymes metabolism, Morphine pharmacology, Receptors, Opioid drug effects
- Abstract
Opioid drugs produce their pharmacological effects by activating inhibitory guanine nucleotide-binding regulatory protein-linked mu, delta, and kappa opioid receptors. One major effector for these receptors is adenylyl cyclase, which is inhibited upon receptor activation. However, little is known about which of the ten known forms of adenylyl cyclase are involved in mediating opioid actions. Here we show that all of the major behavioral effects of morphine, including locomotor activation, analgesia, tolerance, reward, and physical dependence and withdrawal symptoms, are attenuated in mice lacking adenylyl cyclase type 5 (AC5), a form of adenylyl cyclase that is highly enriched in striatum. Furthermore, the behavioral effects of selective mu or delta opioid receptor agonists are lost in AC5-/- mice, whereas the behavioral effects of selective kappa opioid receptor agonists are unaffected. These behavioral data are consistent with the observation that the ability of a mu or delta opioid receptor agonist to suppress adenylyl cyclase activity was absent in striatum of AC5-/- mice. Together, these results establish AC5 as an important component of mu and delta opioid receptor signal transduction mechanisms in vivo and provide further support for the importance of the cAMP pathway as a critical mediator of opioid action.
- Published
- 2006
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22. Regulation of dopaminergic transmission and cocaine reward by the Clock gene.
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McClung CA, Sidiropoulou K, Vitaterna M, Takahashi JS, White FJ, Cooper DC, and Nestler EJ
- Subjects
- Animals, Blotting, Western, Brain metabolism, CLOCK Proteins, Circadian Rhythm, Dose-Response Relationship, Drug, Electrophysiology, Homozygote, Immunohistochemistry, Male, Mice, Mice, Transgenic, Models, Neurological, Mutation, Neurons metabolism, Oligonucleotide Array Sequence Analysis, Phenotype, Phosphorylation, Point Mutation, Time Factors, Tyrosine 3-Monooxygenase metabolism, Ventral Tegmental Area metabolism, Cocaine pharmacology, Dopamine metabolism, Reward, Substance-Related Disorders, Trans-Activators genetics, Trans-Activators physiology, Ventral Tegmental Area physiology
- Abstract
Although there are clear interactions between circadian rhythms and drug addiction, mechanisms for such interactions remain unknown. Here we establish a role for the Clock gene in regulating the brain's reward circuit. Mice lacking a functional Clock gene display an increase in cocaine reward and in the excitability of dopamine neurons in the midbrain ventral tegmental area, a key brain reward region. These phenotypes are associated with increased expression and phosphorylation of tyrosine hydroxylase (the rate-limiting enzyme in dopamine synthesis), as well as changes in several genes known to regulate dopamine activity in the ventral tegmental area. These findings demonstrate the involvement of a circadian-associated gene, Clock, in regulating dopamine function and cocaine reward.
- Published
- 2005
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23. Regulation of anxiety and initiation of sexual behavior by CREB in the nucleus accumbens.
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Barrot M, Wallace DL, Bolaños CA, Graham DL, Perrotti LI, Neve RL, Chambliss H, Yin JC, and Nestler EJ
- Subjects
- Animals, Anti-Anxiety Agents pharmacology, Gene Expression Regulation drug effects, Male, Rats, Rats, Sprague-Dawley, Sexual Behavior, Animal drug effects, Social Isolation, Transcription, Genetic drug effects, Anxiety physiopathology, Cyclic AMP Response Element-Binding Protein metabolism, Nucleus Accumbens physiology, Sexual Behavior, Animal physiology
- Abstract
Sexual deficits and other behavioral disturbances such as anxiety-like behaviors can be observed in animals that have undergone social isolation, especially in species having important social interactions. Using a model of protracted social isolation in adult rats, we observed increased anxiety-like behavior and deficits in both the latency to initiate sexual behavior and the latency to ejaculate. We show, using transgenic cAMP response element (CRE)-LacZ reporter mice, that protracted social isolation also reduces CRE-dependent transcription within the nucleus accumbens. This decrease in CRE-dependent transcription can be mimicked in nonisolated animals by local viral gene transfer of a dominant negative mutant of CRE-binding protein (CREB). We previously showed that this manipulation increases anxiety-like behavior. We show here that it also impairs initiation of sexual behavior in nonisolated animals, a deficit that can be corrected by anxiolytic drug treatment. This local reduction in CREB activity, however, has no influence on ejaculation parameters. Reciprocally, we used the viral transgenic approach to overexpress CREB in the nucleus accumbens of isolated animals. We show that this local increase in CREB activity completely rescued the anxiety phenotype of the isolated animals, as well as their deficit in initiating sexual behavior, but failed to rescue the deficit in ejaculation. Our data suggest a role for the nucleus accumbens in anxiety responses and in specific aspects of sexual behavior. The results also provide insight into the molecular mechanisms by which social interactions affect brain plasticity and behavior.
- Published
- 2005
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24. Essential role of brain-derived neurotrophic factor in adult hippocampal function.
- Author
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Monteggia LM, Barrot M, Powell CM, Berton O, Galanis V, Gemelli T, Meuth S, Nagy A, Greene RW, and Nestler EJ
- Subjects
- Animals, Antidepressive Agents, Tricyclic metabolism, Brain-Derived Neurotrophic Factor genetics, Desipramine metabolism, Electrophysiology, Hippocampus cytology, In Situ Hybridization, Learning physiology, Mice, Mice, Knockout, Brain-Derived Neurotrophic Factor metabolism, Hippocampus metabolism, Motor Activity physiology
- Abstract
Brain-derived neurotrophic factor (BDNF) regulates neuronal development and function. However, it has been difficult to discern its role in the adult brain in influencing complex behavior. Here, we use a recently developed inducible knockout system to show that deleting BDNF in broad forebrain regions of adult mice impairs hippocampal-dependent learning and long-term potentiation. We use the inducible nature of this system to show that the loss of BDNF during earlier stages of development causes hyperactivity and more pronounced hippocampal-dependent learning deficits. We also demonstrate that the loss of forebrain BDNF attenuates the actions of desipramine, an antidepressant, in the forced swim test, suggesting the involvement of BDNF in antidepressant efficacy. These results establish roles for BDNF in the adult, and demonstrate the strength of this inducible knockout system in studying gene function in the adult brain.
- Published
- 2004
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25. Essential role for RGS9 in opiate action.
- Author
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Zachariou V, Georgescu D, Sanchez N, Rahman Z, DiLeone R, Berton O, Neve RL, Sim-Selley LJ, Selley DE, Gold SJ, and Nestler EJ
- Subjects
- Alternative Splicing, Analgesics, Opioid pharmacology, Animals, Blotting, Western, Central Nervous System metabolism, Dose-Response Relationship, Drug, Gene Transfer Techniques, Immunohistochemistry, In Situ Hybridization, Male, Mice, Mice, Inbred C57BL, Mice, Knockout, Morphine metabolism, Morphine pharmacology, Rats, Rats, Sprague-Dawley, Spinal Cord pathology, Temperature, Time Factors, Narcotics metabolism, RGS Proteins physiology
- Abstract
Regulators of G protein signaling (RGS) are a family of proteins known to accelerate termination of effector stimulation after G protein receptor activation. RGS9-2, a brain-specific splice variant of the RGS9 gene, is highly enriched in striatum and also expressed at much lower levels in periaqueductal gray and spinal cord, structures known to mediate various actions of morphine and other opiates. Morphine exerts its acute rewarding and analgesic effects by activation of inhibitory guanine nucleotide-binding regulatory protein-coupled opioid receptors, whereas chronic morphine causes addiction, tolerance to its acute analgesic effects, and profound physical dependence by sustained activation of these receptors. We show here that acute morphine administration increases expression of RGS9-2 in NAc and the other CNS regions, whereas chronic exposure decreases RGS9-2 levels. Mice lacking RGS9 show enhanced behavioral responses to acute and chronic morphine, including a dramatic increase in morphine reward, increased morphine analgesia with delayed tolerance, and exacerbated morphine physical dependence and withdrawal. These findings establish RGS9 as a potent negative modulator of opiate action in vivo, and suggest that opiate-induced changes in RGS9 levels contribute to the behavioral and neural plasticity associated with chronic opiate administration.
- Published
- 2003
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26. CREB activity in the nucleus accumbens shell controls gating of behavioral responses to emotional stimuli.
- Author
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Barrot M, Olivier JD, Perrotti LI, DiLeone RJ, Berton O, Eisch AJ, Impey S, Storm DR, Neve RL, Yin JC, Zachariou V, and Nestler EJ
- Subjects
- Animals, Cyclic AMP Response Element-Binding Protein genetics, Genes, Reporter, Mice, Mice, Transgenic, Pain physiopathology, Rats, Stereotaxic Techniques, Substance-Related Disorders physiopathology, Transcription, Genetic, beta-Galactosidase genetics, Anxiety physiopathology, Avoidance Learning physiology, Conditioning, Psychological physiology, Cyclic AMP Response Element-Binding Protein physiology, Emotions physiology, Nucleus Accumbens physiology
- Abstract
The transcription factor cAMP response element (CRE)-binding protein (CREB) has been shown to regulate neural plasticity. Drugs of abuse activate CREB in the nucleus accumbens, an important part of the brain's reward pathways, and local manipulations of CREB activity have been shown to affect cocaine reward, suggesting an active role of CREB in adaptive processes that follow exposure to drugs of abuse. Using CRE-LacZ reporter mice, we show that not only rewarding stimuli such as morphine, but also aversive stimuli such as stress, activate CRE-mediated transcription in the nucleus accumbens shell. Using viral-mediated gene transfer to locally alter the activity of CREB, we show that this manipulation affects morphine reward, as well as the preference for sucrose, a more natural reward. We then show that local changes in CREB activity induce a more general syndrome, by altering reactions to anxiogenic, aversive, and nociceptive stimuli as well. Increased CREB activity in the nucleus accumbens shell decreases an animal's responses to each of these stimuli, whereas decreased CREB activity induces an opposite phenotype. These results show that environmental stimuli regulate CRE-mediated transcription within the nucleus accumbens shell, and that changes in CREB activity within this brain area subsequently alter gating between emotional stimuli and their behavioral responses. This control appears to be independent of the intrinsic appetitive or aversive value of the stimulus. The potential relevance of these data to addiction and mood disorders is discussed.
- Published
- 2002
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27. DeltaFosB: a sustained molecular switch for addiction.
- Author
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Nestler EJ, Barrot M, and Self DW
- Subjects
- Animals, Brain physiopathology, Humans, Models, Neurological, Neurons physiology, Brain physiology, Genes, fos, Proto-Oncogene Proteins c-fos genetics, Substance-Related Disorders genetics, Substance-Related Disorders physiopathology
- Abstract
The longevity of some of the behavioral abnormalities that characterize drug addiction has suggested that regulation of neural gene expression may be involved in the process by which drugs of abuse cause a state of addiction. Increasing evidence suggests that the transcription factor DeltaFosB represents one mechanism by which drugs of abuse produce relatively stable changes in the brain that contribute to the addiction phenotype. DeltaFosB, a member of the Fos family of transcription factors, accumulates within a subset of neurons of the nucleus accumbens and dorsal striatum (brain regions important for addiction) after repeated administration of many kinds of drugs of abuse. Similar accumulation of DeltaFosB occurs after compulsive running, which suggests that DeltaFosB may accumulate in response to many types of compulsive behaviors. Importantly, DeltaFosB persists in neurons for relatively long periods of time because of its extraordinary stability. Therefore, DeltaFosB represents a molecular mechanism that could initiate and then sustain changes in gene expression that persist long after drug exposure ceases. Studies in inducible transgenic mice that overexpress either DeltaFosB or a dominant negative inhibitor of the protein provide direct evidence that DeltaFosB causes increased sensitivity to the behavioral effects of drugs of abuse and, possibly, increased drug seeking behavior. This work supports the view that DeltaFosB functions as a type of sustained "molecular switch" that gradually converts acute drug responses into relatively stable adaptations that contribute to the long-term neural and behavioral plasticity that underlies addiction.
- Published
- 2001
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28. Dopamine receptor regulating factor, DRRF: a zinc finger transcription factor.
- Author
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Hwang CK, D'Souza UM, Eisch AJ, Yajima S, Lammers CH, Yang Y, Lee SH, Kim YM, Nestler EJ, and Mouradian MM
- Subjects
- 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine pharmacology, Amino Acid Sequence, Animals, Autoradiography, Cell Line, Cocaine pharmacology, Conserved Sequence, Corpus Striatum metabolism, Dopamine metabolism, Dopamine Antagonists pharmacology, Down-Regulation, Gene Expression Regulation drug effects, Haloperidol pharmacology, In Situ Hybridization, Kruppel-Like Transcription Factors, Male, Mice, Mice, Inbred C57BL, Molecular Sequence Data, Neuroblastoma, RNA, Messenger analysis, Receptors, Dopamine metabolism, Sequence Alignment, Sequence Homology, Amino Acid, Transcription Factors chemistry, Transfection, Tumor Cells, Cultured, Zinc Fingers, Brain metabolism, Gene Expression Regulation physiology, Neurons metabolism, Receptors, Dopamine genetics, Transcription Factors genetics, Transcription Factors metabolism
- Abstract
Dopamine receptor genes are under complex transcription control, determining their unique regional distribution in the brain. We describe here a zinc finger type transcription factor, designated dopamine receptor regulating factor (DRRF), which binds to GC and GT boxes in the D1A and D2 dopamine receptor promoters and effectively displaces Sp1 and Sp3 from these sequences. Consequently, DRRF can modulate the activity of these dopamine receptor promoters. Highest DRRF mRNA levels are found in brain with a specific regional distribution including olfactory bulb and tubercle, nucleus accumbens, striatum, hippocampus, amygdala, and frontal cortex. Many of these brain regions also express abundant levels of various dopamine receptors. In vivo, DRRF itself can be regulated by manipulations of dopaminergic transmission. Mice treated with drugs that increase extracellular striatal dopamine levels (cocaine), block dopamine receptors (haloperidol), or destroy dopamine terminals (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine) show significant alterations in DRRF mRNA. The latter observations provide a basis for dopamine receptor regulation after these manipulations. We conclude that DRRF is important for modulating dopaminergic transmission in the brain.
- Published
- 2001
- Full Text
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29. Opiates inhibit neurogenesis in the adult rat hippocampus.
- Author
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Eisch AJ, Barrot M, Schad CA, Self DW, and Nestler EJ
- Subjects
- Animals, Cell Differentiation drug effects, Male, Narcotics pharmacology, Rats, Rats, Sprague-Dawley, Analgesics, Opioid pharmacology, Heroin pharmacology, Hippocampus cytology, Hippocampus drug effects, Morphine pharmacology, Neurons cytology, Neurons drug effects
- Abstract
Recent work implicates regulation of neurogenesis as a form of plasticity in the adult rat hippocampus. Given the known effects of opiates such as morphine and heroin on hippocampal function, we examined opiate regulation of neurogenesis in this brain region. Chronic administration of morphine decreased neurogenesis by 42% in the adult rat hippocampal granule cell layer. A similar effect was seen in rats after chronic self-administration of heroin. Opiate regulation of neurogenesis was not mediated by changes in circulating levels of glucocorticoids, because similar effects were seen in rats that received adrenalectomy and corticosterone replacement. These findings suggest that opiate regulation of neurogenesis in the adult rat hippocampus may be one mechanism by which drug exposure influences hippocampal function.
- Published
- 2000
- Full Text
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30. FosB mutant mice: loss of chronic cocaine induction of Fos-related proteins and heightened sensitivity to cocaine's psychomotor and rewarding effects.
- Author
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Hiroi N, Brown JR, Haile CN, Ye H, Greenberg ME, and Nestler EJ
- Subjects
- Animals, Brain drug effects, Brain metabolism, Immunohistochemistry, Male, Mice, Mice, Mutant Strains, Proto-Oncogene Proteins c-fos biosynthesis, Cocaine pharmacology, Motivation, Proto-Oncogene Proteins c-fos genetics, Psychomotor Performance drug effects
- Abstract
Chronic exposure to cocaine leads to prominent, long-lasting changes in behavior that characterize a state of addiction. The striatum, including the nucleus accumbens and caudoputamen, is an important substrate for these actions. We previously have shown that long-lasting Fos-related proteins of 35-37 kDa are induced in the striatum by chronic cocaine administration. In the present study, the identity and functional role of these Fos-related proteins were examined using fosB mutant mice. The striatum of these mice completely lacked basal levels of the 35- to 37-kDa Fos-related proteins as well as their induction by chronic cocaine administration. This deficiency was associated with enhanced behavioral responses to cocaine: fosB mutant mice showed exaggerated locomotor activation in response to initial cocaine exposures as well as robust conditioned place preference to a lower dose of cocaine, compared with wild-type littermates. These results establish the long-lasting Fos-related proteins as products of the fosB gene (specifically DeltaFosB isoforms) and suggest that transcriptional regulation by fosB gene products plays a critical role in cocaine-induced behavioral responses. This finding demonstrates that a Fos family member protein plays a functional role in behavioral responses to drugs of abuse and implicates fosB gene products as important determinants of cocaine abuse.
- Published
- 1997
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31. Chronic morphine induces visible changes in the morphology of mesolimbic dopamine neurons.
- Author
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Sklair-Tavron L, Shi WX, Lane SB, Harris HW, Bunney BS, and Nestler EJ
- Subjects
- Animals, Cell Size drug effects, Drug Administration Schedule, Morphine pharmacology, Neurons ultrastructure, Rats, Rats, Sprague-Dawley, Brain-Derived Neurotrophic Factor pharmacology, Dopamine physiology, Morphine administration & dosage, Morphine Dependence pathology, Ventral Tegmental Area drug effects
- Abstract
The mesolimbic dopamine system, which arises in the ventral tegmental area (VTA), is an important neural substrate for opiate reinforcement and addiction. Chronic exposure to opiates is known to produce biochemical adaptations in this brain region. We now show that these adaptations are associated with structural changes in VTA dopamine neurons. Individual VTA neurons in paraformaldehyde-fixed brain sections from control or morphine-treated rats were injected with the fluorescent dye Lucifer yellow. The identity of the injected cells as dopaminergic or nondopaminergic was determined by immunohistochemical labeling of the sections for tyrosine hydroxylase. Chronic morphine treatment resulted in a mean approximately 25% reduction in the area and perimeter of VTA dopamine neurons. This reduction in cell size was prevented by concomitant treatment of rats with naltrexone, an opioid receptor antagonist, as well as by intra-VTA infusion of brain-derived neurotrophic factor. In contrast, chronic morphine treatment did not alter the size of nondopaminergic neurons in the VTA, nor did it affect the total number of dopaminergic neurons in this brain region. The results of these studies provide direct evidence for structural alterations in VTA dopamine neurons as a consequence of chronic opiate exposure, which could contribute to changes in mesolimbic dopamine function associated with addiction.
- Published
- 1996
- Full Text
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32. Regulation of expression of cAMP response element-binding protein in the locus coeruleus in vivo and in a locus coeruleus-like cell line in vitro.
- Author
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Widnell KL, Russell DS, and Nestler EJ
- Subjects
- Animals, Base Sequence, Cell Line, Colforsin pharmacology, Cyclic AMP metabolism, Cyclic AMP Response Element-Binding Protein genetics, Gene Expression, In Vitro Techniques, Male, Mice, Molecular Sequence Data, Oligodeoxyribonucleotides chemistry, PC12 Cells, Promoter Regions, Genetic, RNA, Messenger genetics, Rats, Rats, Sprague-Dawley, Cyclic AMP Response Element-Binding Protein metabolism, Locus Coeruleus physiology
- Abstract
Expression of the cAMP response element (CRE)-binding protein (CREB) has been thought to be constitutive and not subject to regulation. In the course of investigating effects of chronic morphine on the cAMP pathway in the locus coeruleus, a brain region important for opiate addiction, we found that levels of CREB immunoreactivity and CRE binding were increased by chronic morphine administration. To further investigate possible mechanisms underlying this unexpected finding, we studied the regulation of CREB expression in a cell line (CATH.a) that exhibits many properties of locus coeruleus neurons. Agents that activate the cAMP pathway led to a > 60% decrease in CREB mRNA in this cell line. Moreover, these alterations in CREB mRNA levels were associated with changes in levels of CREB immunoreactivity and CRE-binding activity. In contrast, the same treatments fail to alter CREB expression in PC12 pheochromocytoma cells.
- Published
- 1994
- Full Text
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33. Regulation of immediate early gene expression and AP-1 binding in the rat nucleus accumbens by chronic cocaine.
- Author
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Hope B, Kosofsky B, Hyman SE, and Nestler EJ
- Subjects
- Animals, Dose-Response Relationship, Drug, Male, Proto-Oncogene Proteins c-fos metabolism, RNA, Messenger genetics, Rats, Rats, Inbred Strains, Cocaine pharmacology, Gene Expression Regulation drug effects, Genes, fos, Genes, jun, Nucleus Accumbens physiology, Proto-Oncogene Proteins c-jun metabolism, Substance-Related Disorders genetics
- Abstract
Chronic treatment of rats with cocaine leads to long-term biochemical changes in the nucleus accumbens (NAc), a brain region implicated in mediating the reinforcing effects of cocaine and other drugs of abuse. Immediate early genes (IEGs) and their protein products appear to play an important role in transducing extracellular stimuli into altered patterns of cellular gene expression and, therefore, into long-term changes in cellular functioning. We therefore examined changes in the mRNA levels for the IEGs c-fos, c-jun, fosB, junB, and zif268 in the NAc of rats treated acutely and chronically with cocaine. A single cocaine injection increased the mRNA levels of all of the IEGs examined. Following chronic cocaine treatment, however, IEG expression had returned to control levels and was not significantly increased following a further acute challenge with cocaine, suggesting desensitization in the ability of cocaine to induce these IEGs. Similarly, levels of Fos-like immunoreactivity, which are increased in the NAc by acute cocaine, were reduced to control levels in chronic cocaine-treated rats. Fos, Jun, and a number of related proteins activate or repress transcription of genes by binding to DNA response elements called AP-1 sites. As would be expected from the RNA data and immunohistochemistry, acute cocaine administration increased AP-1 binding activity in the NAc, an effect that reverted completely to control levels within 8-12 hr. In contrast, AP-1 binding activity in the NAc of animals treated chronically with cocaine remained elevated at acute levels 18 hr after the last chronic injection, a time at which c-fos and c-jun mRNA levels and Fos-like immunoreactivity had returned to control values. An additional acute cocaine challenge did not further increase AP-1 binding. The data suggest that chronic cocaine treatment leads to a persistent increase in AP-1 binding activity, which may be involved in some of the physiological and behavioral aspects of cocaine addiction.
- Published
- 1992
- Full Text
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34. Chronic lithium regulates the expression of adenylate cyclase and Gi-protein alpha subunit in rat cerebral cortex.
- Author
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Colin SF, Chang HC, Mollner S, Pfeuffer T, Reed RR, Duman RS, and Nestler EJ
- Subjects
- Adenylyl Cyclases metabolism, Animals, Blotting, Northern, Cerebral Cortex drug effects, GTP-Binding Proteins metabolism, Isoenzymes metabolism, Lithium Chloride, Macromolecular Substances, Male, Molecular Weight, RNA genetics, RNA isolation & purification, RNA, Messenger genetics, RNA, Messenger isolation & purification, Rats, Rats, Inbred Strains, Adenylyl Cyclases genetics, Cerebral Cortex physiology, Chlorides pharmacology, GTP-Binding Proteins genetics, Gene Expression Regulation, Enzymologic drug effects, Isoenzymes genetics, Lithium pharmacology
- Abstract
A possible role for adenylate cyclase and guanine nucleotide-binding proteins (G proteins) in contributing to the chronic actions of lithium on brain function was investigated in rat cerebral cortex. It was found that chronic treatment of rats with lithium (with therapeutically relevant serum levels of approximately 1 mM) increased levels of mRNA and protein for the calmodulin-sensitive (type 1) and calmodulin-insensitive (type 2) forms of adenylate cyclase and decreased levels of mRNA and protein for the inhibitory G-protein subunits Gi alpha 1 and Gi alpha 2. Chronic lithium did not alter levels of other G-protein subunits, including Go alpha, Gs alpha, and G beta. Lithium regulation of adenylate cyclase and Gi alpha was not seen in response to short-term lithium treatment (with final serum levels of approximately 1 mM) or in response to chronic treatment at a lower dose of lithium (with serum levels of approximately 0.5 mM). The results suggest that up-regulation of adenylate cyclase and down-regulation of Gi alpha could represent part of the molecular mechanism by which lithium alters brain function and exerts its clinical actions in the treatment of affective disorders.
- Published
- 1991
- Full Text
- View/download PDF
35. Chronic antidepressant administration decreases the expression of tyrosine hydroxylase in the rat locus coeruleus.
- Author
-
Nestler EJ, McMahon A, Sabban EL, Tallman JF, and Duman RS
- Subjects
- Animals, Blotting, Northern, Locus Coeruleus drug effects, Male, RNA, Messenger drug effects, RNA, Messenger genetics, RNA, Messenger isolation & purification, Rats, Rats, Inbred Strains, Reference Values, Substantia Nigra drug effects, Substantia Nigra enzymology, Tyrosine 3-Monooxygenase biosynthesis, Antidepressive Agents pharmacology, Gene Expression Regulation, Enzymologic drug effects, Locus Coeruleus enzymology, Tyrosine 3-Monooxygenase genetics
- Abstract
Regulation of tyrosine hydroxylase expression by antidepressant treatments was investigated in the locus coeruleus (LC), the major noradrenergic nucleus in brain. Rats were treated chronically with various antidepressants, and tyrosine hydroxylase levels were measured in the LC by immunoblot analysis. Representatives of all major classes of antidepressant medication-including imipramine, nortriptyline, tranylcypromine, fluvoxamine, fluoxetine, bupropion, iprindole, and electroconvulsive seizures-were found to decrease levels of tyrosine hydroxylase immunoreactivity by 40-70% in the LC. Decreased levels of enzyme immunoreactivity were shown to be associated with equivalent decreases in enzyme mRNA levels. Antidepressant regulation of LC tyrosine hydroxylase appeared specific to these compounds, inasmuch as chronic treatment of rats with representatives of other classes of psychotropic drugs, including haloperidol, diazepam, clonidine, cocaine, and morphine, failed to decrease levels of this protein. The results demonstrate that chronic antidepressants dramatically downregulate the expression of tyrosine hydroxylase in the LC and raise the possibility that such regulation of the enzyme represents an adaptive response of LC neurons to antidepressants that mediates some of their therapeutic actions in depression and/or other psychiatric disturbances.
- Published
- 1990
- Full Text
- View/download PDF
36. Dopamine and depolarizing agents regulate the state of phosphorylation of protein I in the mammalian superior cervical sympathetic ganglion.
- Author
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Nestler EJ and Greengard P
- Subjects
- 1-Methyl-3-isobutylxanthine pharmacology, Animals, Calcium pharmacology, Cattle, Ganglia, Sympathetic metabolism, Membrane Potentials drug effects, Phentolamine pharmacology, Potassium pharmacology, Veratridine pharmacology, Dopamine pharmacology, Ganglia, Sympathetic drug effects, Nerve Tissue Proteins metabolism, Phosphoproteins metabolism
- Abstract
The regulation of the state of phosphorylation of protein I, a specific neuronal protein that appears to be associated predominantly with synaptic vesicles, has been studied in intact sections of bovine superior cervical ganglion. For this purpose, a technique was developed that made possible the quantitation of the state of phosphorylation of as little as 5 fmol of protein I. Incubation of ganglion sections in the presence of dopamine, 8-bromo-cyclic AMP, or depolarizing agents (i.e., high K+ concentration or veratridine) increased the state of phosphorylation of protein I relative to that of control ganglion sections. Other results indicated that the effect of dopamine is probably mediated via the activation of a cyclic AMP-dependent protein kinase and that the effect of high K+ concentration is probably mediated via the activation of a calcium-dependent protein kinase.
- Published
- 1980
- Full Text
- View/download PDF
37. Distribution of protein I in mammalian brain as determined by a detergent-based radioimmunoassay.
- Author
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Goelz SE, Nestler EJ, Chehrazi B, and Greengard P
- Subjects
- Animals, Brain Mapping, Cats, Cattle, Cerebral Cortex metabolism, Detergents, Humans, Phosphoproteins metabolism, Rabbits, Radioimmunoassay, Rats, Synapsins, Brain metabolism, Nerve Tissue Proteins metabolism
- Abstract
A radioimmunoassay has been developed for measuring protein I, a basic, neuron-specific protein associated with nerve terminals. The procedure utilizes the detergents NaDodSO4 and Nonidet P-40 to prevent nonspecific adsorption of this highly charged protein to various surfaces. By use of this procedure, it has been possible to show that protein I comprises approximately 0.4% of the total protein in cerebral cortex of several mammalian species. In addition, the amount of protein I was determined in about 40 regions of cat brain. The results suggest that measurement of protein I may provide a quantitative method for estimating the density of nerve terminals in various regions of the mammalian nervous system.
- Published
- 1981
- Full Text
- View/download PDF
38. Corticosterone differentially regulates the expression of Gs alpha and Gi alpha messenger RNA and protein in rat cerebral cortex.
- Author
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Saito N, Guitart X, Hayward M, Tallman JF, Duman RS, and Nestler EJ
- Subjects
- Adenosine Diphosphate Ribose metabolism, Adrenalectomy, Animals, Blotting, Northern, Blotting, Western, Molecular Weight, RNA, Messenger genetics, Rats, Rats, Inbred Strains, Cerebral Cortex physiology, Corticosterone pharmacology, GTP-Binding Proteins genetics, Gene Expression Regulation drug effects
- Abstract
The possibility that glucocorticoids regulate specific guanine nucleotide binding regulatory proteins (G proteins) was investigated in rat cerebral cortex. Corticosterone was administered to normal and bilaterally adrenalectomized rats, and hormone regulation of individual G-protein subunits was investigated in cerebral cortex in three ways: (i) immunoblot analysis of subunit protein, (ii) hybridization blot analysis of subunit mRNA, and (iii) ADP-ribosylation analysis of stimulatory G protein (Gs alpha) subunits. Chronic (7 days) corticosterone administration to normal rats increased levels of Gs alpha immunoreactivity, mRNA, and ADP-ribosylation but decreased levels of inhibitory G protein (Gi alpha) mRNA and tended to decrease levels of Gi alpha immunoreactivity. In contrast, levels of Go alpha and G beta immunoreactivity and mRNA were not influenced by corticosterone treatment. In adrenalectomized rats, corticosterone treatment produced a 25-50% increase in the levels of Gs alpha immunoreactivity, mRNA, and ADP-ribosylation, whereas the hormone produced a 20-35% decrease in the levels of Gi alpha immunoreactivity and mRNA. Adrenalectomy, without corticosterone replacement, produced the opposite effects on Gs alpha and Gi alpha compared to sham-operated controls, indicating that these G proteins are regulated by this class of steroid hormone under physiological conditions in vivo. The results indicate that specific G-protein subunits--namely, Gs alpha and Gi alpha--are under the coordinated control of glucocorticoids in rat brain and demonstrate that G proteins are physiological targets of glucocorticoids in vivo. Possible roles played by these G-protein responses in mediating the effects of glucocorticoids on brain function are discussed.
- Published
- 1989
- Full Text
- View/download PDF
39. Cellular and subcellular localization of protein I in the peripheral nervous system.
- Author
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Fried G, Nestler EJ, De Camilli P, Stjärne L, Olson L, Lundberg JM, Hökfelt T, Ouimet CC, and Greengard P
- Subjects
- Adrenal Glands innervation, Adrenal Medulla analysis, Animals, Denervation, Dopamine beta-Hydroxylase analysis, Iris analysis, Iris innervation, Norepinephrine analysis, Radioimmunoassay, Rats, Subcellular Fractions analysis, Synapsins, Nerve Tissue Proteins analysis, Peripheral Nerves analysis, Phosphoproteins analysis
- Abstract
The cellular and subcellular distribution of protein I, a major brain phosphoprotein, has been studied in the peripheral nervous system. The levels of protein I in various peripheral nerves and innervated peripheral tissues were determined by radioimmunoassay and radioimmunolabeling of polyacrylamide gels. The results indicated tha protein I is present throughout the peripheral nervous system. Denervation studies of adrenal medulla and iris suggested that the protein I contained in peripheral tissues is localized to the neuronal elements innervating those tissues. Protein I was found to be enriched in neurotransmitter vesicle fractions of peripheral nervous tissue. Moreover, protein I appeared to be transported from cell bodies to axons terminals at least partly in association with neurotransmitter vesicles.
- Published
- 1982
- Full Text
- View/download PDF
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