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白藜芦醇苷通过增加 GR mRNA 和 BDNF mRNA 逆转失败应激后小鼠的社交回避。

Icaritin opposes the development of social aversion after defeat stress via increases of GR mRNA and BDNF mRNA in mice.

机构信息

Department of Integrative Medicine, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai 200040, China.

出版信息

Behav Brain Res. 2013 Nov 1;256:602-8. doi: 10.1016/j.bbr.2013.09.034. Epub 2013 Sep 21.

Abstract

Icariin is a major constituent of flavonoids isolated from Herba Epimedii. Several previous studies have demonstrated the antidepressant-like effects of icariin. After oral administration of icariin, 19 metabolites of icariin were detected in rat plasma. Icaritin is one such of metabolite of icariin. In this study, a chronic social defeat protocol is used as a mouse model for depression, and the effects of icaritin administration on social avoidance are investigated. The data indicates that icaritin (5mg/kg and 10mg/kg) oral administration opposes the development of social aversion after defeat stress. In vitro corticosterone sensitivity assay demonstrated that icaritin partially restored social defeat-induced impairment of glucocorticoid sensitivity. The expressions of GR mRNA and BDNFmRNA in the hippocampus were increased after icaritin treatment. Meanwhile, the social defeat-induced increases in CRH mRNA in hypothalamus were restored by icaritin administration. Our data also suggests that icaritin administration remarkably attenuated the increases in serum IL-6 and TNF-α level that occur following exposure to social defeat. In conclusion, icaritin is a novel antidepressant. It partially restored social defeat-induced impairment of glucocorticoid sensitivity, HPA axis hyperactivity. These effects are at least partially attributed to normalization of the GR function and increases in BDNF expression.

摘要

朝藿定是从淫羊藿中分离得到的黄酮类化合物的主要成分。多项先前的研究已经证实了朝藿定具有抗抑郁作用。朝藿定经口服给药后,在大鼠血浆中检测到 19 种朝藿定的代谢物。朝藿次苷是朝藿定的一种代谢物。在这项研究中,采用慢性社交挫败协议作为抑郁的小鼠模型,研究了朝藿次苷给药对社交回避的影响。数据表明,朝藿次苷(5mg/kg 和 10mg/kg)口服给药可拮抗败应激后社会回避的发展。体外皮质酮敏感性测定表明,朝藿次苷部分恢复了社交挫败引起的糖皮质激素敏感性损害。朝藿次苷处理后,海马中的 GRmRNA 和 BDNFmRNA 的表达增加。同时,朝藿次苷给药可恢复下丘脑 CRHmRNA 在社交挫败诱导下的增加。我们的数据还表明,朝藿次苷给药可显著减弱暴露于社交挫败后血清 IL-6 和 TNF-α水平的升高。总之,朝藿次苷是一种新型的抗抑郁药。它部分恢复了社交挫败引起的糖皮质激素敏感性损害和 HPA 轴活性亢进。这些作用至少部分归因于 GR 功能的正常化和 BDNF 表达的增加。

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