Multiple actions of a D3 dopamine receptor agonist, PD128907, on GABAergic inhibitory transmission between medium spiny neurons in mouse nucleus accumbens shell

被引:7
|
作者
Kohnomi, Shuntaro [1 ]
Konishi, Shiro [1 ]
机构
[1] Tokushima Bunri Univ, Kagawa Sch Pharmaceut Sci, Dept Neurophysiol, Sanuki Shi, Kagawa 7692193, Japan
基金
日本学术振兴会;
关键词
Dopamine; Dopamine D-3 receptor; GABAergic transmission; Lateral inhibition; Medium spiny neurons; Nucleus accumbens; JAW MOVEMENTS; SYSTEMS;
D O I
10.1016/j.neulet.2015.05.056
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The nucleus accumbens (NAc) plays a crucial role in pathophysiological responses, such as reward-related behaviors, addiction, depression and schizophrenia, through activation of dopaminergic system in the midbrain area. Principal cells in the NAc are medium spiny neurons (MSNs), which constitute the majority (90-95%) of NAc neuron populations in rodents. MSNs are mutually connected to form networks of lateral inhibition. Our previous study showed that activation of D-2-like receptors presynaptically inhibited GABAergic transmission between MSN-MSN connections in the NAc. D-2-like receptors in MSNs have been reported to consist of D-2 and D-3 receptors, but their functional roles remain to be elucidated. This study, therefore, aimed at examining the effects of D-3 receptor activation on MSN-MSN connections using PD128907, a preferential D-3 dopamine receptor agonist, and whole cell recordings from MSNs in acute slices including the NAc. In more than half of cells tested, PD128907 reduced the frequency of spontaneous inhibitory postsynaptic currents (sIPSCs) in a concentration-dependent manner. However, the agonist caused multiple actions, namely, decrease, increase and no significant changes, in the amplitude as well as the frequency of sIPSCs in individual cells. Our data, together with the results from previous studies, show that dopamine could suppress GABAergic transmission, i.e., lateral inhibition between some of MSNs, via activation of both D-2 and D-3 receptors. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:17 / 21
页数:5
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