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外侧隔区参与丙泊酚诱导的焦虑样行为的调节。

The lateral septum partakes the regulation of propofol-induced anxiety-like behavior.

作者信息

Hu Qian, Cai Huajing, Ke Xinlong, Wang Hongwei, Zheng Du, Chen Yeru, Wang Yongjie, Chen Gang

机构信息

Department of Anesthesiology, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, 310058, China.

School of Pharmacy, Hangzhou Normal University, Hangzhou, Zhejiang, 311121, China.

出版信息

Eur J Pharmacol. 2024 Aug 15;977:176756. doi: 10.1016/j.ejphar.2024.176756. Epub 2024 Jun 18.

Abstract

Repeated exposure to propofol during early brain development is associated with anxiety disorders in adulthood, yet the mechanisms underlying propofol-induced susceptibility to anxiety disorders remain elusive. The lateral septum (LS), primarily composed of γ-aminobutyric acidergic (GABAergic) neurons, serves as a key brain region in the regulation of anxiety. However, it remains unclear whether LS GABAergic neurons are implicated in propofol-induced anxiety. Therefore, we conducted c-Fos immunostaining of whole-brain slices from mice exposed to propofol during early life. Our findings indicate that propofol exposure activates GABAergic neurons in the LS. Selective activation of LS GABAergic neurons resulted in increased anxiety-like behavior, while selective inhibition of these neurons reduced such behaviors. These results suggest that the LS is a critical brain region involved in propofol-induced anxiety. Furthermore, we investigated the molecular mechanism of propofol-induced anxiety in the LS. Microglia activation underlies the development of anxiety. Immunofluorescence staining and Western blot analysis of LS revealed activated microglia and significantly elevated levels of phospho-NF-κB p65 protein. Additionally, a decrease in the number of neuronal spines was observed. Our study highlights the crucial role of the LS in the development of anxiety-like behavior in adulthood following childhood propofol exposure, accompanied by the activation of inflammatory pathways.

摘要

在大脑发育早期反复接触丙泊酚与成年期焦虑症有关,但丙泊酚导致易患焦虑症的潜在机制仍不清楚。外侧隔核(LS)主要由γ-氨基丁酸能(GABA能)神经元组成,是调节焦虑的关键脑区。然而,尚不清楚LS的GABA能神经元是否与丙泊酚诱导的焦虑有关。因此,我们对生命早期接触丙泊酚的小鼠全脑切片进行了c-Fos免疫染色。我们的研究结果表明,接触丙泊酚会激活LS中的GABA能神经元。选择性激活LS的GABA能神经元会导致焦虑样行为增加,而选择性抑制这些神经元则会减少此类行为。这些结果表明,LS是参与丙泊酚诱导焦虑的关键脑区。此外,我们研究了丙泊酚在LS中诱导焦虑的分子机制。小胶质细胞激活是焦虑症发生的基础。对LS进行免疫荧光染色和蛋白质印迹分析显示小胶质细胞激活,且磷酸化核因子κB p65蛋白水平显著升高。此外,还观察到神经元棘突数量减少。我们的研究强调了LS在儿童期接触丙泊酚后成年期焦虑样行为发展中的关键作用,并伴有炎症途径的激活。

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