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Farnesoid X receptor-mediated cytoplasmic translocation of CRTC2 disrupts CREB-BDNF signaling in hippocampal CA1 and leads to the development of depression-like behaviors in mice.
International Journal of Neuropsychopharmacology ( IF 4.5 ) Pub Date : 2020-05-26 , DOI: 10.1093/ijnp/pyaa039
Wenfeng Hu 1 , Jingjing Wu 2 , Ting Ye 1 , Zhuo Chen 3 , Jinhua Tao 1 , Lijuan Tong 1 , Kai Ma 1, 4 , Jie Wen 5 , Hui Wang 1 , Chao Huang 1
Affiliation  

We recently identified neuronal expression of farnesoid X receptor (FXR), a bile acid receptor known to impair autophagy by inhibiting cyclic adenosine monophosphate response element-binding protein (CREB), a protein whose under-functioning is linked to neuroplasticity and depression. In this study, we hypothesize that FXR may mediate depression via a CREB-dependent mechanism.

中文翻译:

Farnesoid X 受体介导的 CRTC2 细胞质易位破坏了海马 CA1 中的 CREB-BDNF 信号传导,并导致小鼠出现抑郁样行为。

我们最近确定了法尼醇 X 受体 (FXR) 的神经元表达,这是一种胆汁酸受体,已知通过抑制环磷酸腺苷反应元件结合蛋白 (CREB) 来损害自噬,CREB ​​是一种功能不足与神经可塑性和抑郁有关的蛋白质。在这项研究中,我们假设 FXR 可能通过 CREB ​​依赖性机制介导抑郁症。
更新日期:2020-05-26
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