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Annual recruitment in fish is undoubtedly impacted by a vast number of biotic and abiotic factors. That is especially the case for fish species such as the black bass (species in the genus Micropterus), where there is extended parental care. Although much focus has been given in the past on determining the roles that many of these factors (e.g., temperatures, wind, flow rates, and habitat change) play in determining recruitment among the back basses, little attention has been given to assessing what role reproductive success plays in that determination. To address this question, we conducted a long-term study on two adjacent smallmouth bass (SMB) Micropterus dolomieu Lacepede, 1802 populations in eastern ON to assess the relationship between annual fry cohort size (FCS) (i.e., population-wide reproductive success) and annual recruitment. To measure population-wide annual FCS, we used snorkel surveys to conduct a complete census of nesting SMB males during the spawn from 1990 to 2015. During those surveys, we quantified mating success, determined which nests were successful or not, and calculated the number of independent fry produced each year by summing those numbers across all successful nests. Summer snorkel surveys from 1991 to 2016 assessed annual recruitment through visual counts of age 1+ juveniles. Results demonstrated a highly significant, positive, linear relationship between annual FCS and annual recruitment. Key words: smallmouth bass, Micropterus dolomieu, annual recruitment, reproductive success, angling, Introduction Smallmouth bass (SMB) Micropterus dolomieu Lacepede, 1802 and largemouth bass M. salmoides (Lacepede, 1802), two of the species in the genus commonly referred to as black bass, are both [...]

A new programmable trigger board and digital mean-timer modules using complex programmable logic device have been introduced to the trigger system of the BNL-E949 experiment. The online dead time was reduced from 4.0% to 1.7% by introducing an on-chip prescaler to the programmable trigger board. The acceptance loss of the online photon veto was reduced from 4.9% to 1.8% by introducing the mean-timer modules. Index Terms--Complex programmable logic device (CPLD), field-programmable gate array (FPGA), mean-timer, trigger.

The retromer complex is an evolutionarily conserved protein complex involved in the endosomal recycling of various cargo proteins. It is ubiquitously expressed in all tissue and is found in both invertebrate as well as mammalian nervous systems, where it recycles various synaptic membrane proteins including the dopamine transporter and dopamine D1 receptor, two proteins implicated in dopamine homeostasis and neurotransmission. The involvement of the retromer complex in dopamine neurobiology is further underscored by its links to Parkinson's disease, a neurodegenerative disorder of the dopamine system. In this article, the existing literature linking the retromer complex to synaptic function and dopamine homeostasis is reviewed. Additional possible links are highlighted by exploring the retromer and other Parkinson's disease‐associated proteins and possible relationships to synaptic function and dopamine transmission. [ABSTRACT FROM AUTHOR]

Using an in vitro model of ischemic stroke we treated differentiated SH-SY5Y cells to oxygen-glucose deprivation (OGD) followed by a reperfusion period where normal growth conditions were restored. Cells undergoing OGD exhibited significant cell death as measure by propidium iodide staining. However, cells treated with exogenous extracellular DJ-1 during reperfusion exhibited significant rescue from OGD-induced cell death. [ABSTRACT FROM AUTHOR]

Abstract: Parkinson''s disease (PD) is a neurodegenerative disease characterized by a loss of nigrostriatal dopaminergic neurons. Recently, PD research has been stimulated by the identification of genes that are implicated in rare familial forms of PD. However, despite these discoveries, the primary cause of PD is still unclear. Various pathogenic mechanisms may be involved including mitochondrial dysfunction, proteasomal dysfunction/protein aggregation, oxidative damage, environmental factors and genetic disposition. Furthermore, dopamine has also been implicated in contributing to the pathogenesis of PD. This review will focus on the genes that have been identified to be associated with PD and how they may impair dopamine metabolism. Understanding the role of these PD-related genes in dopamine neurobiology may provide insight into the underpinning pathogenic mechanisms of PD. [Copyright &y& Elsevier]

Dopamine is a major neurotransmitter in the mammalian central nervous system (CNS) that regulates neuroendocrine functions, locomotor activity, cognition and emotion. The dopamine system has been extensively studied because dysfunction of this system is linked to various pathological conditions including Parkinson's disease, schizophrenia, Tourette's syndrome, and drug addiction. Accordingly, intense efforts to delineate the full complement of signaling pathways mediated by individual receptor subtypes have been pursued. Dopamine D1-like receptors are of particular interest because they are the most abundant dopamine receptors in CNS. Recent work suggests that dopamine signaling could be regulated via dopamine receptor interacting proteins (DRIPs). Unraveling these DRIPs involved in the dopamine system may provide a better understanding of the mechanisms underlying CNS disorders related to dopamine system dysfunction and may help identify novel therapeutic targets. [ABSTRACT FROM AUTHOR]

Abstract: Recent research suggests that basal ganglia dysfunction may result in problems integrating concurrent vision and proprioception during movement. We evaluated dopaminergic system involvement in this sensorimotor process during locomotion within a large sample of Parkinson’s disease (PD) patients while “On” and “Off” their dopaminergic medications (n=25), in conditions that selectively manipulated the availability of proprioception, vision or both. The present experiment focused on two main objectives: i) to examine the relative influence of visual and proprioceptive inputs on locomotion and target accuracy in patients with PD; and ii) to examine the influence of dopamine replacement therapy on sensorimotor integration while moving toward the target. All participants walked at a self-selected pace on a GAITRite® carpet in two baseline conditions (light and dark), as well as four experimental darkness conditions: a) to a remembered target (i.e. proprioception only), b) to a remembered target with light on chest for body position awareness (proprioception plus), c) with vision of a lit target, also with light on chest (vision and proprioception), d) pushed in wheelchair to remembered target (no proprioception or vision). Final position was measured by 2-D radial error, and revealed a group by condition interaction, suggesting that PD patients “Off” their medications move to targets with less accuracy, but approach the accuracy of healthy participants when in the “On” state. Both PD and healthy improved their accuracy with availability of concurrent vision and proprioception (condition c). Interestingly, our results demonstrate that PD “Off” performed the task with greater difficulty than when “On” medication, but only when proprioception was the sole source of feedback. Since PD, whether medicated or unmedicated were even more affected when proprioception was removed (wheelchair), a memory-related explanation can be ruled out. Our results suggest that the basal ganglia are not specifically involved in visuoproprioceptive integration; however, assimilation of proprioceptive feedback to guide an ongoing movement may be a critical function of the basal ganglia. [Copyright &y& Elsevier]

Focuses on the dual regulation of NMDA receptor functions by direct protein-protein interactions with the dopamine D1 receptor. Contents of Dopamine D1-like receptors; Calcium permeability of NMDA receptor; Dependence of NMDA-mediated excitoxicity on local cellular environment.

The mechanism by which dopaminergic neurons are selectively lost in Parkinson disease (PD) is unknown. Here we show that accumulation of α-synuclein in cultured human dopaminergic neurons results in apoptosis that requires endogenous dopamine production and is mediated by reactive oxygen species. In contrast, α-synuclein is not toxic in non-dopaminergic human cortical neurons, but rather exhibits neuroprotective activity. Dopamine-dependent neurotoxicity is mediated by 54?83-kD soluble protein complexes that contain α-synuclein and 14-3-3 protein, which are elevated selectively in the substantia nigra in PD. Thus, accumulation of soluble α-synuclein protein complexes can render endogenous dopamine toxic, suggesting a potential mechanism for the selectivity of neuronal loss in PD. [ABSTRACT FROM AUTHOR]

Examines the subcellular distribution of dystrophin in isolated adult and neonatal cardiac myocytes. Dystrophin as a protein product of Duchenne muscular dystrophy (DMD) gene; Presence in T-tubular membrane; Use of immunocytochemical studies; Excitation-contraction coupling; Cytoskeleton of muscle cells.

Background: Although dopamine D1 receptors are involved in working memory, how D1 receptors contribute to this process remains unclear. Numerous studies have shown that D1 receptors have extensive functional interaction with N-methyl-D-aspartate (NMDA) receptor. Our group previously demonstrated that D1 receptors were able to regulate NMDA receptor functions through direct protein–protein interactions involving the carboxyl terminals of D1 receptors and NMDA receptor NR1a and NR2A subunits respectively. In this study, we explored the effects of the D1–NR1 interaction on NMDA receptor-dependent long-term potentiation (LTP) and working memory by using the TAT-conjugated interfering peptide (TAT-D1-t2). Methods: Miniature excitatory postsynaptic currents are recorded in rat hippocampal primary cultures. Coimmunoprecipitation and calcium/calmodulin-dependent protein kinase II (CaMKII) activity are measured in hippocampal slices and hippocampal neurons under the specified experimental conditions, respectively. Working memory was assessed using a delayed match-to-place protocol in the Morris Water Maze following administration of the TAT-D1-t2 peptide. Results: Electrophysiology experiments showed that activation of D1 receptor upregulates NMDA receptor-mediated LTP in a CaMKII-dependent manner. Furthermore, D1 receptor agonist stimulation promotes the NR1-CaMKII coupling and enhances the CaMKII activity; and the D1 receptor-mediated effects can be blocked by the application of the TAT-D1-t2 peptide. Interestingly, animals injected with TAT-D1-t2 peptide exhibited significantly impaired working memory. Conclusions: Our study showed a critical role of NMDA-D1 direct protein–protein interaction in NMDA receptor–mediated LTP and working memory and implicated the involvement of CaMKII in this process. [Copyright &y& Elsevier]

Summary: The molecular underpinnings of exploration and its link to learning and memory remain poorly understood. Here we show that inducible, modest overexpression of neuronal calcium sensor 1 (Ncs1) selectively in the adult murine dentate gyrus (DG) promotes a specific form of exploratory behavior. The mice also display a selective facilitation of long-term potentiation (LTP) in the medial perforant path and a selective enhancement in rapid-acquisition spatial memory, phenotypes that are reversed by direct application of a cell-permeant peptide (DNIP) designed to interfere with NCS-1 binding to the dopamine type-2 receptor (D2R). Moreover, the DNIP and the D2R-selective antagonist L-741,626 attenuated exploratory behavior, DG LTP, and spatial memory in control mice. These data demonstrate a role for NCS-1 and D2R in DG plasticity and provide insight for understanding how the DG contributes to the origin of exploration and spatial memory acquisition. [Copyright &y& Elsevier]