中国神经再生研究(英文版) ›› 2022, Vol. 17 ›› Issue (3): 632-642.doi: 10.4103/1673-5374.320993

• 原著:脑损伤修复保护与再生 • 上一篇    下一篇

淫羊藿苷对抗抑郁症中海马神经发生障碍的机制

  

  • 出版日期:2022-03-15 发布日期:2021-10-15

Exploration of the mechanism by which icariin modulates hippocampal neurogenesis in a rat model of depression

Ning-Xi Zeng#, Hui-Zhen Li#, Han-Zhang Wang, Kai-Ge Liu, Xia-Yu Gong, Wu-Long Luo, Can Yan*, Li-Li Wu*   

  1. Research Center for Basic Integrative Medicine, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong Province, China
  • Online:2022-03-15 Published:2021-10-15
  • Contact: Li-Li Wu, PhD, wulili@gzucm.edu.cn; Can Yan, PhD, yc1970@gzucm.edu.cn.
  • Supported by:
    This study was supported by the National Natural Science Foundation of China, No. 81774102 (to LLW).

摘要:

淫羊藿苷具有明显的抗抑郁和抗海马损伤作用,但其不能有效地穿越血脑屏障在大脑内蓄积,因此其抗抑郁症海马损伤的机制有待进一步揭示。实验以脑脊液蛋白质组学为基础,探索淫羊藿苷抗抑郁海马神经发生功能障碍的机制。(1)首先将大鼠暴露于慢性不可预知轻度应激环境6周建立抑郁模型,同时每天腹腔注射淫羊藿苷(120 mg / kg)进行干预。发现淫羊藿苷能减轻抑郁大鼠的抑郁症状、学习记忆障碍、神经发生障碍和减少神经元丢失;(2)将大鼠胚胎海马神经干细胞置于含20%淫羊藿苷干预的大鼠脑脊液中预培养,再以100 μM皮质酮模拟应激损伤,可明显改善高浓度皮质酮抑制神经元的增殖和分化;(3)以蛋白质组学方法筛选了脑脊液中由慢性应激和淫羊藿苷共同调控的52种差异表达的蛋白,这些蛋白主要参与核糖体通路、PI3K-Akt信号通路与白细胞介素17通路;(4)平行反应监测定量分析结果表明,Rps4x、Rps12、Rps14、Rps19、Hsp90b1和Hsp90aa1可被慢性应激上调,被淫羊藿苷下调;HtrA1则可被慢性应激下调,被淫羊藿苷上调;(5)表明淫羊藿苷可通过调节脑脊液中某些蛋白表达而发挥抗抑郁和抗海马神经发生障碍的作用。实验于2017年3月经广州中医药大学实验动物伦理委员会批准。

https://orcid.org/0000-0002-3643-9010 (Li-Li Wu); https://orcid.org/0000-0003-0680-5099 (Can Yan)

关键词: 抑郁症, 海马神经发生障碍, 淫羊藿苷, 慢性应激, 海马, 核糖体通路, 脑脊液, 蛋白质组学

Abstract: Icariin (ICA) has a significant capacity to protect against depression and hippocampal injury, but it cannot effectively cross the blood-brain barrier and accumulate in the brain. Therefore, the mechanism by which ICA protects against hippocampal injury in depression remains unclear. In this study, we performed proteomics analysis of cerebrospinal fluid to investigate the mechanism by which ICA prevents dysfunctional hippocampal neurogenesis in depression. A rat model of depression was established through exposure to chronic unpredictable mild stress for 6 weeks, after which 120 mg/kg ICA was administered subcutaneously every day. The results showed that ICA alleviated depressive symptoms, learning and memory dysfunction, dysfunctional neurogenesis, and neuronal loss in the dentate gyrus of rats with depression. Neural stem cells from rat embryonic hippocampi were cultured in media containing 20% cerebrospinal fluid from each group of rats and then treated with 100 μM corticosterone. The addition of cerebrospinal fluid from rats treated with ICA largely prevented the corticosterone-mediated inhibition of neuronal proliferation and differentiation. Fifty-two differentially expressed proteins regulated by chronic unpredictable mild stress and ICA were identified through proteomics analysis of cerebrospinal fluid. These proteins were mainly involved in the ribosome, PI3K-Akt signaling, and interleukin-17 signaling pathways. Parallel reaction monitoring mass spectrometry showed that Rps4x, Rps12, Rps14, Rps19, Hsp90b1, and Hsp90aa1 were up-regulated by chronic unpredictable mild stress and down-regulated by ICA. In contrast, HtrA1 was down-regulated by chronic unpredictable mild stress and up-regulated by ICA. These findings suggest that ICA can prevent depression and dysfunctional hippocampal neurogenesis through regulating the expression of certain proteins found in the cerebrospinal fluid. The study was approved by the Experimental Animal Ethics Committee of Guangzhou University of Chinese Medicine of China in March 2017.

Key words: cerebrospinal fluid, chronic unpredictable mild stress, depression, dysfunctional hippocampal neurogenesis, hippocampus, icariin, proteomics, ribosome pathway

中图分类号: