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      Attenuated inhibition of medium spiny neurons participates in the pathogenesis of childhood depression

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          Abstract

          Accumulating evidence suggests that the nucleus accumbens, which is involved in mechanisms of reward and addiction, plays a role in the pathogenesis of depression and in the action of antidepressants. In the current study, intraperitoneal injection of nomifensine, a dopamine reuptake inhibitor, decreased depression-like behaviors in the Wistar Kyoto rat model of depression in the sucrose-preference and forced swim tests. Nomifensine also reduced membrane excitability in medium spiny neurons in the core of the nucleus accumbens in the childhood Wistar Kyoto rats as evaluated by electrophysiological recording. In addition, the expression of dopamine D2-like receptor mRNA was downregulated in the nucleus accumbens, striatum and hippocampus of nomifensine-treated childhood Wistar Kyoto rats. These experimental findings indicate that impaired inhibition of medium spiny neurons, mediated by dopamine D2-like receptors, may be involved in the formation of depression-like behavior in childhood Wistar Kyoto rats, and that nomifensine can alleviate depressive behaviors by reducing medium spiny neuron membrane excitability.

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          Most cited references62

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          Reward and aversion in a heterogeneous midbrain dopamine system.

          The ventral tegmental area (VTA) is a heterogeneous brain structure that serves a central role in motivation and reward processing. Abnormalities in the function of VTA dopamine (DA) neurons and the targets they influence are implicated in several prominent neuropsychiatric disorders including addiction and depression. Recent studies suggest that the midbrain DA system is composed of anatomically and functionally heterogeneous DA subpopulations with different axonal projections. These findings may explain a number of previously confusing observations that suggested a role for DA in processing both rewarding as well as aversive events. Here we will focus on recent advances in understanding the neural circuits mediating reward and aversion in the VTA and how stress as well as drugs of abuse, in particular cocaine, alter circuit function within a heterogeneous midbrain DA system. This article is part of a Special Issue entitled 'NIDA 40th Anniversary Issue'. Copyright © 2013 Elsevier Ltd. All rights reserved.
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            Physiology and pharmacology of striatal neurons.

            The basal ganglia occupy the core of the forebrain and consist of evolutionarily conserved motor nuclei that form recurrent circuits critical for motivation and motor planning. The striatum is the main input nucleus of the basal ganglia and a key neural substrate for procedural learning and memory. The vast majority of striatal neurons are spiny GABAergic projection neurons, which exhibit slow but temporally precise spiking in vivo. Contributing to this precision are several different types of interneurons that constitute only a small fraction of total neuron number but play a critical role in regulating striatal output. This review examines the cellular physiology and modulation of striatal neurons that give rise to their unique properties and function.
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              Bregma, lambda and the interaural midpoint in stereotaxic surgery with rats of different sex, strain and weight.

              Craniometric and stereotaxic data from rats of different sex, strain and weight were compared. It was found that stereotaxic atlases can be used with rats of different sex and strain provided that the weights of the rats conform to those used in the reference atlas. If rats of different weights are used, greater accuracy can be achieved if bregma is used as the reference point for work with rostral structures and the interaural line for work with caudal structures.
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                Author and article information

                Journal
                Neural Regen Res
                Neural Regen Res
                NRR
                Neural Regeneration Research
                Medknow Publications & Media Pvt Ltd (India )
                1673-5374
                1876-7958
                15 May 2014
                : 9
                : 10
                : 1079-1088
                Affiliations
                [1]Bio-X Institutes, Shanghai Jiao Tong University, Shanghai, China
                Author notes
                Corresponding author: Shengtian Li, Bio-X Institutes, Shanghai Jiao Tong University, Shanghai 200240, China, lstian@ 123456sjtu.edu.cn .

                Author contributions: Liu DD and Li ST designed the study. Liu DD, Hu LH, Zhang JQ and Zhang P conducted experiments. Liu DD and Li ST analyzed the data and wrote the manuscript. All authors approved the final version of the manuscript .

                Article
                NRR-9-1079
                10.4103/1673-5374.133171
                4146299
                73493116-07c1-4708-97e3-5f351c0d0b4a
                Copyright: © Neural Regeneration Research

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 11 April 2014
                Categories
                Technical Updates

                nerve regeneration,brain injury,neurophysiology,msns,dopamine d2-like receptors,childhood depression,wistar kyoto rats,nucleus accumbens,excitatory inhibition,neural plasticity,nomifensine,nsfc grant,neural regeneration

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