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大脑奖励回路中的中脑边缘多巴胺神经元介导对社交挫败的易感性和抗抑郁作用。

Mesolimbic dopamine neurons in the brain reward circuit mediate susceptibility to social defeat and antidepressant action.

机构信息

Department of Psychiatry, University of Texas Southwestern Medical Center, Dallas, Texas 75390-9070, USA.

出版信息

J Neurosci. 2010 Dec 8;30(49):16453-8. doi: 10.1523/JNEUROSCI.3177-10.2010.

Abstract

We previously reported that the activity of mesolimbic dopamine neurons of the ventral tegmental area (VTA) is a key determinant of behavioral susceptibility vs resilience to chronic social defeat stress. However, this was based solely on ex vivo measurements, and the in vivo firing properties of VTA dopamine neurons in susceptible and resilient mice, as well as the effects of antidepressant treatments, remain completely unknown. Here, we show that chronic (10 d) social defeat stress significantly increased the in vivo spontaneous firing rates and bursting events in susceptible mice but not in the resilient subgroup. Both the firing rates and bursting events were significantly negatively correlated with social avoidance behavior, a key behavioral abnormality induced by chronic social defeat stress. Moreover, the increased firing rates, bursting events, and avoidance behavior in susceptible mice were completely reversed by chronic (2 week), but not acute (single dose), treatments with the antidepressant medication fluoxetine (20 mg/kg). Chronic social defeat stress increased hyperpolarization-activated cation current (I(h)) in VTA dopamine neurons, an effect that was also normalized by chronic treatment with fluoxetine. As well, local infusion of I(h) inhibitors ZD7288 (0.1 μg) or DK-AH 269 (0.6 μg) into the VTA exerted antidepressant-like behavioral effects. Together, these data suggest that the firing patterns of mesolimbic dopamine neurons in vivo mediate an individual's responses to chronic stress and antidepressant action.

摘要

我们之前曾报道,腹侧被盖区(VTA)的中脑边缘多巴胺神经元的活动是决定个体对慢性社会挫败应激易感性和弹性的关键因素。然而,这仅仅基于离体测量,易感和弹性小鼠的 VTA 多巴胺神经元的体内放电特性以及抗抑郁治疗的效果仍然完全未知。在这里,我们表明慢性(10 天)社会挫败应激显著增加了易感小鼠的体内自发放电率和爆发事件,但在弹性亚组中没有增加。放电率和爆发事件与慢性社会挫败应激诱导的关键行为异常——社交回避行为呈显著负相关。此外,易感小鼠的放电率、爆发事件和回避行为增加可被慢性(2 周)而非急性(单次剂量)抗抑郁药物氟西汀(20mg/kg)治疗完全逆转。慢性社会挫败应激增加了 VTA 多巴胺神经元中的超极化激活阳离子电流(I(h)),氟西汀的慢性治疗也使这种效应正常化。此外,将 I(h)抑制剂 ZD7288(0.1μg)或 DK-AH 269(0.6μg)局部输注到 VTA 中可发挥抗抑郁样的行为效应。综上所述,这些数据表明,中脑边缘多巴胺神经元的体内放电模式介导了个体对慢性应激和抗抑郁作用的反应。

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