Involvement of nucleus accumbens D2-medium spiny neurons projecting to the ventral pallidum in anxiety-like behaviour

被引:5
|
作者
Correia, Raquel [2 ,3 ,4 ]
Coimbra, Barbara [2 ,3 ,4 ]
Domingues, Ana Veronica [2 ,3 ,4 ]
Wezik, Marcelina [2 ,3 ,4 ]
Vieitas-Gaspar, Natacha [2 ,3 ,4 ]
Gaspar, Rita [2 ,3 ,4 ]
Sousa, Nuno [2 ,3 ,4 ,5 ]
Pinto, Luisa [2 ,3 ,4 ]
Rodrigues, Ana Joao [1 ,2 ,3 ,4 ,5 ]
Soares-Cunha, Carina [1 ,2 ,3 ,4 ]
机构
[1] Univ Minho, Sch Med, ICVS, Campus Gualtar, P-4710057 Braga, Portugal
[2] Univ Minho, Life & Hlth Sci Res Inst ICVS, Sch Med, Braga, Portugal
[3] ICVS 3Bs PT Govt Associate Lab, Braga, Portugal
[4] ICVS 3Bs PT Govt Associate Lab, Guimaraes, Portugal
[5] Clin Acad Ctr Braga, Braga, Portugal
来源
JOURNAL OF PSYCHIATRY & NEUROSCIENCE | 2023年 / 48卷 / 04期
基金
欧洲研究理事会;
关键词
DOPAMINE NEURONS; PATHWAYS; ENCODE; STIMULATION; ACTIVATION; DEPRESSION; AVOIDANCE; STRIATUM; CORE;
D O I
10.1503/jpn.220111
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background:The nucleus accumbens (NAcc) is a crucial brain region for emotionally relevant behaviours. The NAcc is mainly composed of medium spiny neurons (MSNs) expressing either dopamine receptor D1 (D1-MSNs) or D2 (D2-MSNs). The D1-MSNs project to the ventral tegmental area (VTA) and the ventral pallidum (VP), whereas the D2-MSNs project only to the VP. The D1- and D2-MSNs have been associated with depression-like behaviours, but their contribution to anxiety remains to be determined. Methods:We used optogenetic tools to selectively manipulate D1-MSN projections from the NAcc core to the VP or VTA and D2-MSN projections to the VP during validated anxiety-producing behavioural procedures in naive mice. In addition, we assessed the effects of optical stimulation on neuronal activity using in vivo electrophysiologic recordings in anesthetized animals. Results:Optogenetic activation of D1-MSN projections to the VTA or VP did not trigger anxiety-like behaviour. However, optical activation of D2-MSN projections to the VP significantly increased anxiety-like behaviour. This phenotype was associated with a decrease in the neuronal activity of putative GABAergic neurons in the VP. Importantly, pretreating D2-MSN-VP animals with the & gamma;-aminobutyric acid modulator diazepam prevented the optically triggered anxiety-like behaviour. Limitations:The exclusive use of males in the behavioural tests limits broader interpretation of the findings. Although we used optogenetic conditions that trigger quasi-physiologic changes, there are caveats associated with the artificial manipulation of neuronal activity. Conclusion:The D2-MSN-VP projections contributed to the development of anxiety-like behaviour, through modulation of GABAergic activity in the VP.
引用
收藏
页码:E267 / E284
页数:18
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