Department of Integrative Medicine, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai 200040, China.
Behav Brain Res. 2013 Nov 1;256:602-8. doi: 10.1016/j.bbr.2013.09.034. Epub 2013 Sep 21.
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.
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。