15 results on '"Noguchi, K."'
Search Results
2. Dorsal column-thalamic pathway is involved in thalamic hyperexcitability following peripheral nerve injury: a lesion study in rats with experimental mononeuropathy.
- Author
-
Miki, K, Iwata, K, Tsuboi, Y, Morimoto, T, Kondo, E, Dai, Y, Ren, K, and Noguchi, K
- Published
- 2000
- Full Text
- View/download PDF
3. Change in mRNAs for neuropeptides and the GABA(A) receptor in dorsal root ganglion neurons in a rat experimental neuropathic pain model.
- Author
-
Fukuoka, T, Tokunaga, A, Kondo, E, Miki, K, Tachibana, T, Noguchi, K, Fukuoka, Tetsuo, Tokunaga, Atsushi, Kondo, Eiji, Miki, Kenji, Tachibana, Toshiya, and Noguchi, Koichi
- Published
- 1998
- Full Text
- View/download PDF
4. Responses of dorsal column nuclei neurons in rats with experimental mononeuropathy.
- Author
-
Miki, K, Iwata, K, Tsuboi, Y, Sumino, R, Fukuoka, T, Tachibana, T, Tokunaga, A, Noguchi, K, Miki, Kenji, Iwata, Koichi, Tsuboi, Yoshiyuki, Sumino, Rhyuji, Fukuoka, Tetsuo, Tachibana, Toshiya, Tokunaga, Atsushi, and Noguchi, Koichi
- Published
- 1998
- Full Text
- View/download PDF
5. A selective increase in Fos expression in spinal dorsal horn neurons following graded thermal stimulation in rats with experimental mononeuropathy
- Author
-
Dai, Y., Iwata, K., Kondo, E., Morimoto, T., and Noguchi, K.
- Published
- 2001
- Full Text
- View/download PDF
6. The role of evolving concepts and new technologies and approaches in advancing pain research, management, and education since the establishment of the International Association for the Study of Pain.
- Author
-
Flor H, Noguchi K, Treede RD, and Turk DC
- Subjects
- Humans, Pain Management methods, Chronic Pain therapy
- Abstract
Abstract: The decades since the inauguration of the International Association for the Study of Pain have witnessed major advances in scientific concepts (such as the biopsychosocial model and chronic primary pain as a disease in its own right) and in new technologies and approaches (from molecular biology to brain imaging) that have inspired innovations in pain research. These have guided progress in pain management and education about pain for healthcare professionals, the general public, and administrative agencies., (Copyright © 2023 International Association for the Study of Pain.)
- Published
- 2023
- Full Text
- View/download PDF
7. Re-evaluation of the phenotypic changes in L4 dorsal root ganglion neurons after L5 spinal nerve ligation.
- Author
-
Fukuoka T, Yamanaka H, Kobayashi K, Okubo M, Miyoshi K, Dai Y, and Noguchi K
- Subjects
- Activating Transcription Factor 3 metabolism, Animals, Brain-Derived Neurotrophic Factor metabolism, Disease Models, Animal, Ligation, Male, Neuropeptide Y metabolism, Rats, Rats, Sprague-Dawley, Spinal Nerves metabolism, Ganglia, Spinal metabolism, Neuralgia metabolism, Neurons metabolism, Sodium Channels metabolism, Spinal Nerves injuries
- Abstract
The L5 spinal nerve ligation (SNL) is a widely used animal neuropathic pain model. There are conflicting reports regarding the extent of injury to the L4 dorsal root ganglion (DRG) neurons in this model. If a significant number of these neurons were injured, the previously reported phenotypic and electrophysiological changes at this level are in need of re-evaluation by separating the injured neurons and the frankly spared ones. So, we immunostained activating transcription factor 3 (ATF3) and examined the change in expression of transcripts for neuropeptide Y (NPY), brain-derived neurotrophic factor (BDNF) and several voltage-gated sodium channel α-subunits (Nav1.1, Nav1.3, Nav1.6, Nav1.7, Nav1.8, and Nav1.9) in the L4 DRG by comparing signal intensities of individual neurons using in situ hybridization histochemistry. ATF3-immunoreactivity was similarly observed in 4-6% of neuronal nuclei of the SNL and sham-operated ipsilateral L4 DRGs. Comparison between ATF3+ and ATF3- neurons in the SNL L4 DRG revealed that (1) whereas NPY induction occurred in ATF3+ cells, BDNF increased mainly in ATF3- neurons; (2) although ATF3+ neurons had higher Nav1.3 signals than ATF3- neurons, these signals were much lower than those of the L5 DRG neurons; and (3) ATF3+/N52- neurons selectively lost Nav1.8 and Nav1.9 mRNAs. Comparison of the total neuronal populations among naïve, SNL, and sham-operated rats revealed no significant differences for all examined Nav mRNAs. Because neuropathic pain behaviors were developed by rats with SNL but not the sham-operation, the small number of injured L4 neurons likely do not contribute to the pathomechanisms of neuropathic pain., (Copyright © 2011 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.)
- Published
- 2012
- Full Text
- View/download PDF
8. The role of ERK signaling and the P2X receptor on mechanical pain evoked by movement of inflamed knee joint.
- Author
-
Seino D, Tokunaga A, Tachibana T, Yoshiya S, Dai Y, Obata K, Yamanaka H, Kobayashi K, and Noguchi K
- Subjects
- Adenosine Triphosphate analogs & derivatives, Adenosine Triphosphate therapeutic use, Animals, Axonal Transport, Butadienes therapeutic use, Disease Models, Animal, Freund's Adjuvant toxicity, Ganglia, Spinal pathology, Hyperalgesia etiology, Hyperalgesia physiopathology, Injections, Intra-Articular, Injections, Spinal, Male, Neurons, Afferent drug effects, Neurons, Afferent physiology, Nitriles therapeutic use, Pain etiology, Phosphorylation drug effects, Purinergic P2 Receptor Antagonists, Rats, Rats, Sprague-Dawley, Receptors, Purinergic P2X3, Signal Transduction, Stifle innervation, Stress, Mechanical, Arthritis, Experimental physiopathology, Extracellular Signal-Regulated MAP Kinases physiology, Osteoarthritis, Knee physiopathology, Pain physiopathology, Protein Processing, Post-Translational drug effects, Range of Motion, Articular, Receptors, Purinergic P2 physiology
- Abstract
Pain during inflammatory joint diseases is enhanced by the generation of hypersensitivity in nociceptive neurons in the peripheral nervous system. To explore the signaling mechanisms of mechanical hypersensitivity during joint inflammation, experimental arthritis was induced by injection of complete Freund's adjuvant (CFA) into the synovial cavity of rat knee joints. As a pain index, the struggle threshold of the knee extension angle was measured. In rats with arthritis, the phosphorylation of extracellular signal-regulated kinase (ERK), induced by passive joint movement, increased significantly in dorsal root ganglion (DRG) neurons innervating the knee joint compared to the naïve rats that received the same movement. The intrathecal injection of a MEK inhibitor, U0126, reduced the phosphorylation of ERK in DRG neurons and alleviated the struggle behavior elicited by the passive movement of the joint. In addition, the injection of U0126 into the joint also reduced the struggle behavior. These findings indicate that the ERK signaling is activated in both cell bodies in DRG neurons and peripheral nerve fibers and may be involved in the mechanical sensitivity of the inflamed joint. Furthermore, the phosphorylated ERK-positive neurons co-expressed the P2X3 receptor, and the injection of TNP-ATP, which antagonizes P2X receptors, into the inflamed joint reduced the phosphorylated ERK and the struggle behavior. Thus, it is suggested that the activation of the P2X3 receptor is involved in the phosphorylation of ERK in DRG neurons and the mechanical hypersensitivity of the inflamed knee joint.
- Published
- 2006
- Full Text
- View/download PDF
9. Activation of p38 MAPK in primary afferent neurons by noxious stimulation and its involvement in the development of thermal hyperalgesia.
- Author
-
Mizushima T, Obata K, Yamanaka H, Dai Y, Fukuoka T, Tokunaga A, Mashimo T, and Noguchi K
- Subjects
- Animals, Capsaicin pharmacology, Cell Count methods, Dose-Response Relationship, Drug, Dose-Response Relationship, Radiation, Drug Interactions, Hot Temperature, Hyperalgesia etiology, Immunohistochemistry methods, Ion Channels metabolism, Male, Mitogen-Activated Protein Kinase 6 metabolism, Neurofilament Proteins metabolism, Neurons drug effects, Pain Measurement drug effects, Pain Measurement radiation effects, Pyrazoles pharmacology, Pyridines pharmacology, Rats, Rats, Sprague-Dawley, TRPV Cation Channels, Time Factors, p38 Mitogen-Activated Protein Kinases antagonists & inhibitors, Enzyme Activation physiology, Ganglia, Spinal cytology, Hyperalgesia metabolism, Neurons enzymology, p38 Mitogen-Activated Protein Kinases metabolism
- Abstract
Alterations in the intracellular signal transduction pathway in primary afferents may contribute to pain hypersensitivity. We demonstrated that very rapid phosphorylation of p38 mitogen-activated protein kinase occurred in dorsal root ganglion (DRG) neurons that were participating in the transmission of noxious signals. Capsaicin injection induced phosphorylated-p38 (p-p38) in small-to-medium diameter sensory neurons with a peak at 2 min after capsaicin injection. Furthermore, we examined the p-p38 labeling in the DRG after noxious thermal stimuli and found a stimulus intensity-dependent increase in labeled cell size and the number of activated neurons. Most of these p-p38-immunoreactive (IR) neurons were small- and medium-sized neurons, which coexpressed transient receptor potential ion channel TRPV1 and phosphorylated-extracellular signal-regulated protein kinase. Intrathecal administration of the p38 inhibitor, FR167653, reversed the thermal hyperalgesia produced by the capsaicin injection. Inhibition of p38 activation was confirmed by the decrease in the number of p-p38-IR neurons in the DRG following capsaicin injection. Taken together, these findings suggest that the activation of p38 pathways in primary afferents by noxious stimulation in vivo may be, at least in part, correlated with functional activity, and further, involved in the development of thermal hyperalgesia.
- Published
- 2005
- Full Text
- View/download PDF
10. Activation of extracellular signal-regulated protein kinase in dorsal horn neurons in the rat neuropathic intermittent claudication model.
- Author
-
Liu Y, Obata K, Yamanaka H, Dai Y, Fukuoka T, Tokunaga A, and Noguchi K
- Subjects
- Alprostadil administration & dosage, Analysis of Variance, Animals, Butadienes administration & dosage, Disease Models, Animal, Enzyme Inhibitors administration & dosage, Immunohistochemistry methods, Intermittent Claudication drug therapy, Intermittent Claudication physiopathology, MAP Kinase Signaling System physiology, Male, Nitriles administration & dosage, Rats, Rats, Sprague-Dawley, Spinal Stenosis physiopathology, Walking physiology, Alprostadil analogs & derivatives, Intermittent Claudication enzymology, Mitogen-Activated Protein Kinases metabolism, Posterior Horn Cells enzymology
- Abstract
Extracellular signal-regulated protein kinase (ERK) is a mitogen-activated protein kinase (MAPK) that mediates several cellular responses to mitogenic and differentiation signals, and activation of ERK in dorsal horn neurons by noxious stimulation is known to contribute to pain hypersensitivity. In order to elucidate the pathophysiological mechanisms of the cauda equina syndrome, secondary to spinal canal stenosis, we evaluated walking dysfunction triggered by forced exercise and activation of ERK in the dorsal horn using a rat model of neuropathic intermittent claudication. Rats in the lumbar canal stenosis (LCS) group showed a shorter running distance from 1 to 14 days after surgery. Two minutes after running on the treadmill apparatus, phosphorylation of ERK was induced in neurons in the superficial laminae in the LCS group but not in the sham group, whereas there was no change in the deeper laminae. Intrathecal administration of the MAPK kinase inhibitor, U0126, 30 min before running, clearly increased the running distance, whereas there was no significant change in the vehicle control group 3 days after surgery. In addition, a prostaglandin E1 analog, OP-1206 alpha-CD, administered orally, improved the walking dysfunction, and further, inhibited activation of ERK following running 7 days after surgery. These findings suggest that intermittent claudication triggered by forced walking might affect the phosphorylation of ERK in the superficial laminae, possibly via transient (partial) ischemia of the spinal cord. ERK activation in the dorsal horn neurons may be involved in the transient pain in the neuropathic intermittent claudication model.
- Published
- 2004
- Full Text
- View/download PDF
11. Contribution of sensitized P2X receptors in inflamed tissue to the mechanical hypersensitivity revealed by phosphorylated ERK in DRG neurons.
- Author
-
Dai Y, Fukuoka T, Wang H, Yamanaka H, Obata K, Tokunaga A, and Noguchi K
- Subjects
- Adenosine Triphosphate pharmacology, Animals, Cell Count, Disease Models, Animal, Dose-Response Relationship, Drug, Drug Interactions, Freund's Adjuvant, Functional Laterality drug effects, Immunohistochemistry methods, Inflammation chemically induced, Male, Neurofilament Proteins metabolism, Phosphorylation, Physical Stimulation, Platelet Aggregation Inhibitors pharmacology, Purinergic P2 Receptor Agonists, Purinergic P2 Receptor Antagonists, Pyridoxal Phosphate pharmacology, Rats, Rats, Sprague-Dawley, Receptors, Purinergic P2X, Adenosine Triphosphate analogs & derivatives, Ganglia, Spinal cytology, Inflammation metabolism, Mitogen-Activated Protein Kinases metabolism, Neurons metabolism, Pyridoxal Phosphate analogs & derivatives, Receptors, Purinergic P2 metabolism
- Abstract
The mechanism of mechanical hyperalgesia in inflammation might involve a 'mechanochemical' process whereby stretch evokes the release of adenosine 5'-triphosphate (ATP) from the damaged tissue that then excites nearby primary sensory nerve terminals. In the present study, phosphorylated extracellular signal-regulated protein kinase (pERK) immunoreactivity was used as a marker indicating functional activation of primary afferent neurons to examine the P2X receptor-mediated noxious response in DRG neurons in a rat model of peripheral inflammation. We found that very few pERK-labeled DRG neurons were detected in normal rats after alpha, beta methylene-ATP (alphabetame-ATP) intraplantar injection. However, a number of DRG neurons were labeled for pERK after alphabetame-ATP injection to the complete Freund's adjuvant (CFA) induced inflamed paw. Seventy-three percent of pERK-labeled DRG neurons co-expressed the P2X3 receptor. After mechanical noxious stimulation to the hind paw of CFA-inflamed rats, we found many more pERK-labeled neurons compared to those in the normal rats. Administration of the P2X3 receptor antagonists, pyridoxalphosphate-6-azophenyl-2',4'-disulfonic acid or 2'- (or 3')-O-(trinitrophenyl)adenosine 5'-triphosphate (TNP-ATP), significantly decreased the mechanical stimulation-evoked pERK labeling in CFA-inflamed rats, but not in normal rats. We also found the recruitment of neurons with myelinated A fibers labeled for pERK in CFA-inflamed rats, which was reversed by P2X3 receptor antagonists. Moreover, TNP-ATP dose dependently reduced the mechanical hypersensitivity of CFA rats. These data suggest that the P2X receptors in primary afferent neurons increase their activity with enhanced sensitivity of the intracellular ERK signaling pathway during inflammation and then contribute to the hypersensitivity to mechanical noxious stimulation in the inflammatory state.
- Published
- 2004
- Full Text
- View/download PDF
12. Contribution of injured and uninjured dorsal root ganglion neurons to pain behavior and the changes in gene expression following chronic constriction injury of the sciatic nerve in rats.
- Author
-
Obata K, Yamanaka H, Fukuoka T, Yi D, Tokunaga A, Hashimoto N, Yoshikawa H, and Noguchi K
- Subjects
- Activating Transcription Factor 3, Animals, Behavior, Animal, Brain-Derived Neurotrophic Factor analysis, Brain-Derived Neurotrophic Factor genetics, Chronic Disease, Ganglia, Spinal cytology, Gene Expression, Hyperalgesia epidemiology, Hyperalgesia physiopathology, Immunohistochemistry, In Situ Hybridization, Incidence, Male, Neurons, Afferent chemistry, RNA, Messenger analysis, Rats, Rats, Sprague-Dawley, Receptors, GABA-A analysis, Receptors, GABA-A genetics, Sciatica epidemiology, Touch, Transcription Factors analysis, Transcription Factors genetics, Ganglia, Spinal injuries, Neurons, Afferent physiology, Sciatica physiopathology
- Abstract
Neuropathic pain models, such as the chronic constriction injury (CCI) model, are partial nerve injury models where there exist both intact and injured peripheral axons. Recent studies suggested that dorsal root ganglion (DRG) neurons with intact axons also show the alteration of excitability and gene expression and might have some role in the pathophysiological mechanisms of neuropathic pain. The incidence of pain-related behavior after the CCI is unstable and variable. In the present study, we used activating transcription factor 3 (ATF3) expression as a neuronal injury marker, and analyzed a relationship between the number of axotomized neurons and the incidence of pain-related behavior. We divided all rats into three groups according to the percentage of ATF3-immunoreactive (IR) neurons, group 1 (<12.5%), group 2 (12.5-25%), and group 3 (>25%). We found that rats in groups 2 and 3 showed thermal hyperalgesia, whereas only the rats in group 2 developed tactile allodynia from the third day to the fourteenth day after surgery. Rats in group 1 did not show thermal hyperalgesia or tactile allodynia. The DRG neurons in group 2 contained ATF3-IR neurons mainly in medium- and large-sized neurons. In order to investigate brain-derived neurotrophic factor (BDNF) and gamma-aminobutyric acid(A)-receptor (GABA(A)-R) regulation in both intact and injured primary afferent neurons after the CCI, we used a double-labeling method with immunohistochemistry and in situ hybridization, as well as double immunofluorescent staining. The CCI induced an increased number of BDNF-labeled neurons in the ipsilateral DRG and the increase in BDNF expression was observed mainly in small- and medium-sized neurons that were mainly ATF3-negative. On the other hand, the number of GABA(A)-Rgamma2 subunit mRNA-positive neurons decreased in the ipsilateral DRG and GABA(A)-R- and ATF3-labeled neurons rarely overlapped. These changes in molecular phenotype in intact and injured primary afferents may be involved in the pathophysiological mechanisms of neuropathic pain produced by partial nerve injury.
- Published
- 2003
- Full Text
- View/download PDF
13. VR1, but not P2X(3), increases in the spared L4 DRG in rats with L5 spinal nerve ligation.
- Author
-
Fukuoka T, Tokunaga A, Tachibana T, Dai Y, Yamanaka H, and Noguchi K
- Subjects
- Animals, Disease Models, Animal, Ganglia, Spinal cytology, Gene Expression physiology, Hindlimb, Hyperalgesia metabolism, Hyperalgesia physiopathology, Ligation, Lumbar Vertebrae, Male, Neuralgia physiopathology, Neurons, Afferent physiology, Rats, Rats, Sprague-Dawley, Receptors, Drug genetics, Receptors, Purinergic P2 genetics, Receptors, Purinergic P2X3, Spinal Nerves cytology, Spinal Nerves physiology, TRPV Cation Channels, Ganglia, Spinal physiology, Neuralgia metabolism, Receptors, Drug metabolism, Receptors, Purinergic P2 metabolism
- Abstract
We investigated the expression of two candidate transducers of noxious stimuli in peripheral tissues, the vanilloid receptor subtype 1 (VR1) and the P2X(3), a subunit of the ionotropic P2X receptor for ATP, in spared L4 DRG neurons following L5 spinal nerve ligation, a neuropathic pain model. VR1 mRNA expression increased in the small- and medium-sized DRG neurons from the first to 28th day after injury, and this up-regulation corresponded well with the development and maintenance of thermal hyperalgesia of the hind paw. The increase in VR1-immunoreactive (ir) neurons was confirmed at the third day after surgery. In contrast, there was no change in expression of P2X(3) mRNA over 4 weeks after ligation, or in the percentage of P2X(3)-ir neurons observed 3 days after surgery. Our data suggests that increased VR1 in the spared L4 DRG may contribute to the exaggerated heat response observed in this neuropathic pain model. Taken together with the previous reports that P2X(3) expression increases in the spared DRG neurons in other neuropathic pain models, there appears to be differences in the phenotypic changes and pathomechanisms of the various neuropathic pain models., (Copyright 2002 International Association for the Study of Pain)
- Published
- 2002
- Full Text
- View/download PDF
14. Expression of neurotrophic factors in the dorsal root ganglion in a rat model of lumbar disc herniation.
- Author
-
Obata K, Tsujino H, Yamanaka H, Yi D, Fukuoka T, Hashimoto N, Yonenobu K, Yoshikawa H, and Noguchi K
- Subjects
- Animals, Behavior, Animal, Brain-Derived Neurotrophic Factor analysis, Disease Models, Animal, Ganglia, Spinal cytology, Gene Expression physiology, Glial Fibrillary Acidic Protein analysis, Lumbar Vertebrae, Male, Nerve Growth Factor analysis, Nerve Growth Factor pharmacology, Neuritis physiopathology, Neurons, Afferent chemistry, Neurons, Afferent physiology, Peripheral Nerves drug effects, RNA, Messenger analysis, Rats, Rats, Sprague-Dawley, Brain-Derived Neurotrophic Factor genetics, Ganglia, Spinal physiology, Intervertebral Disc Displacement complications, Nerve Growth Factor genetics, Neuralgia physiopathology
- Abstract
A variety of molecules released by inflammatory reactions in the dorsal root and dorsal root ganglion (DRG) may play important roles in the pathology of neuronal abnormalities in lumbar disc herniation. In order to elucidate the pathophysiological mechanisms of painful radiculopathy, secondary to lumbar disc herniation, we evaluated pain-related behavior and the change of nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF) expression in the DRG and dorsal root using a rat model of lumbar disc herniation. In the nucleus pulposus (NP) group, the left L4/5 nerve roots were exposed after hemilaminectomies and autologous intervertebral discs, which were obtained from coccygeal intervertebral discs, were implanted on each of the exposed nerve roots without mechanical compression. Rats in the NP group, but not the sham-operated rats, developed mechanical allodynia on the ipsilateral hind paw for 1 day after surgery and showed a significant increase in the number of NGF-immunoreactive (IR) cells in the nerve root and DRG. NGF-IR cells in the nerve root and DRG included macrophages and Schwann cells, because these cells were labeled for NGF and ED-1 or glial fibrillary acid protein by dual immunostaining. A significant increase in the percentage of BDNF-IR neurons in the DRG was observed in the NP group at 3 days after surgery and the increase in BDNF mRNA expression was confirmed using in situ hybridization histochemistry and reverse transcription-polymerase chain reaction. We also injected NGF into the endoneurial space of the normal rat spinal nerve root and found that the NGF injection produced dose-dependent mechanical allodynia on the ipsilateral hind paw at 1 day after surgery and an increase in the percentage of BDNF-IR neurons in the DRG at 3 days after surgery compared to the group receiving saline injection. These findings suggest that in the lumbar disc herniation model, i.e. neuritis of the nerve root, increased NGF produced by the inflammatory responses in the dorsal root and DRG tissues may affect the production of BDNF in the DRG and may play important roles in the modulation of the dorsal horn neurons. These changes in neurotrophic factors in the primary afferents may be involved in the pathophysiological mechanisms of neuropathic pain produced by lumbar disc herniation., (Copyright 2002 International Association for the Study of Pain)
- Published
- 2002
- Full Text
- View/download PDF
15. Involvement of glutamate receptors on hyperexcitability of wide dynamic range neurons in the gracile nucleus of the rats with experimental mononeuropathy.
- Author
-
Kondo E, Iwata K, Ogawa A, Tashiro A, Tsuboi Y, Fukuoka T, Yamanaka H, Dai Y, Morimoto T, and Noguchi K
- Subjects
- Animals, Male, Medulla Oblongata cytology, Medulla Oblongata drug effects, Neurons drug effects, Rats, Rats, Sprague-Dawley, Sciatic Neuropathy metabolism, Excitatory Amino Acid Antagonists pharmacology, Hyperalgesia metabolism, Medulla Oblongata metabolism, Mononeuropathies metabolism, Neurons metabolism, Receptors, Glutamate physiology
- Abstract
In order to clarify the functional role of glutamate receptors of the gracile nucleus neurons in rats with nerve injury-induced hyperalgesia, pharmacological, electrophysiological and in situ hybridization techniques were used in rats with chronic constriction nerve injury (CCI) of the sciatic nerve. A total of 54 wide dynamic range neurons were recorded from the gracile nucleus in the rats with CCI. Mechanical evoked responses were significantly depressed following application of AMPA receptor antagonist, CNQX, with noxious and non-noxious responses being similarly affected. AP-5, an NMDA receptor antagonist, induced depression of the pressure-evoked response only after application of the 1-microM concentration of this drug. The size of the receptive fields was significantly decreased after CNQX, but not MK-801 or AP-5, application. Afterdischarge was significantly depressed following the application of CNQX (1000 microM). The expression of ionotropic glutamate receptor subunit mRNAs in the gracile nucleus was studied using the in situ hybridization technique. The signals for NMDA subunits, NR2A, -2B and -2C, in the gracile nucleus neurons were not prominent, suggesting a low level expression of functional NMDA receptor complex. AMPA receptor subunits GluR1, -R2, -R3 and -R4 mRNAs were expressed in a large number of gracile nucleus neurons. These data are consistent with the pharmacological results that AMPA receptor antagonists depressed nociceptive neuronal activity, but NMDA receptor antagonists showed limited effects. These results suggest that the ionotropic glutamate receptors, i.e. the AMPA and NMDA receptors, are differentially involved in modulation of the wide dynamic range neuronal activity in the gracile nucleus following peripheral nerve injury.
- Published
- 2002
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.