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一对多巴胺神经元介导慢性应激信号,导致. 的学习能力缺陷。

A pair of dopamine neurons mediate chronic stress signals to induce learning deficit in .

机构信息

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Biology, Hunan University, Changsha 410082, P.R. China.

HHMI, Janelia Research Campus, Ashburn, VA 20147.

出版信息

Proc Natl Acad Sci U S A. 2021 Oct 19;118(42). doi: 10.1073/pnas.2023674118.

Abstract

Chronic stress could induce severe cognitive impairments. Despite extensive investigations in mammalian models, the underlying mechanisms remain obscure. Here, we show that chronic stress could induce dramatic learning and memory deficits in The chronic stress-induced learning deficit (CSLD) is long lasting and associated with other depression-like behaviors. We demonstrated that excessive dopaminergic activity provokes susceptibility to CSLD. Remarkably, a pair of PPL1-γ1pedc dopaminergic neurons that project to the mushroom body (MB) γ1pedc compartment play a key role in regulating susceptibility to CSLD so that stress-induced PPL1-γ1pedc hyperactivity facilitates the development of CSLD. Consistently, the mushroom body output neurons (MBON) of the γ1pedc compartment, MBON-γ1pedc>α/β neurons, are important for modulating susceptibility to CSLD. Imaging studies showed that dopaminergic activity is necessary to provoke the development of chronic stress-induced maladaptations in the MB network. Together, our data support that PPL1-γ1pedc mediates chronic stress signals to drive allostatic maladaptations in the MB network that lead to CSLD.

摘要

慢性应激可导致严重的认知障碍。尽管在哺乳动物模型中进行了广泛的研究,但潜在的机制仍不清楚。在这里,我们表明慢性应激可导致果蝇出现明显的学习和记忆缺陷。慢性应激诱导的学习障碍(CSLD)是持久的,并与其他类似抑郁的行为有关。我们证明,多巴胺能活动过度会引起对 CSLD 的易感性。值得注意的是,一对投射到蘑菇体(MB)γ1pedc 隔室的 PPL1-γ1pedc 多巴胺能神经元在调节对 CSLD 的易感性方面起着关键作用,因此应激诱导的 PPL1-γ1pedc 过度活跃促进了 CSLD 的发展。一致地,γ1pedc 隔室的蘑菇体输出神经元(MBON),MBON-γ1pedc>α/β 神经元,对于调节对 CSLD 的易感性很重要。成像研究表明,多巴胺能活动对于引发 MB 网络中慢性应激诱导的适应不良是必要的。总之,我们的数据支持 PPL1-γ1pedc 将慢性应激信号传递到 MB 网络中,导致 CSLD。

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