无血性
胶质纤维酸性蛋白
前额叶皮质
神经科学
心理学
慢性应激
星形胶质增生
白喉毒素
生物
医学
中枢神经系统
内科学
毒素
认知
免疫组织化学
多巴胺
生物化学
作者
Sierra A. Codeluppi,Meiyu Xu,Yashika Bansal,Ashley E. Lepack,Vanja Đurić,Margaret Chow,Jessie Muir,Rosemary C. Bagot,Pawel Licznerski,Stacey L. Wilber,Gerard Sanacora,Etienne Sibille,Ronald S. Duman,Christopher Pittenger,M. Banasr
标识
DOI:10.1038/s41380-023-02246-1
摘要
Abstract Reductions of astroglia expressing glial fibrillary acidic protein (GFAP) are consistently found in the prefrontal cortex (PFC) of patients with depression and in rodent chronic stress models. Here, we examine the consequences of PFC GFAP+ cell depletion and cell activity enhancement on depressive-like behaviors in rodents. Using viral expression of diphtheria toxin receptor in PFC GFAP+ cells, which allows experimental depletion of these cells following diphtheria toxin administration, we demonstrated that PFC GFAP+ cell depletion induced anhedonia-like behavior within 2 days and lasting up to 8 days, but no anxiety-like deficits. Conversely, activating PFC GFAP+ cell activity for 3 weeks using designer receptor exclusively activated by designer drugs (DREADDs) reversed chronic restraint stress-induced anhedonia-like deficits, but not anxiety-like deficits. Our results highlight a critical role of cortical astroglia in the development of anhedonia and further support the idea of targeting astroglia for the treatment of depression.
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