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北五味子通过增加脑源性神经营养因子的信号传导来抑制睡眠剥夺和慢性不可预测轻度应激引起的行为缺陷。

Schisandrae Chinensis Fructus inhibits behavioral deficits induced by sleep deprivation and chronic unpredictable mild stress via increased signaling of brain-derived neurotrophic factor.

机构信息

School of Functional Food and Wine, Shenyang Pharmaceutical University, Shenyang, China.

School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.

出版信息

Phytother Res. 2019 Dec;33(12):3177-3190. doi: 10.1002/ptr.6489. Epub 2019 Aug 30.

Abstract

The present study was undertaken to explore the interactions between sleep deprivation (SD) and Schisandrae Chinensis Fructus (SCF) treatment in the antidepressant-like effects. We observed that SD aggravated the anxiety-like behavior induced by chronic unpredictable mild stress (CUMS) in the elevated plus maze test. However, the forced swimming test and sucrose preference test showed that SD (12 hr) alleviated the depressive symptoms and SD (72 hr) has the opposite effects. Administration of SCF showed a promising therapeutic effect on depression and anxiety induced by CUMS and SD. Moreover, SCF could potential strengthen the antidepressant-like effects of SD (12 hr) according to the behavioral tests. In addition, the BDNF level in hippocampus was elevated by SD (12 hr) and SCF treatment and together with the upregulation of TrkB/CREB/ERK and PI3K/AKT/GSK3β/mTOR signaling pathways. Besides, the protein levels of p70S6K and PSD95, which are downstream targets of mTOR, also increased by the treatment. These results indicated that the antidepressant-like effect of SCF in the CUMS depends on the activation of BDNF and the modulation of TrkB/CREB/ERK and PI3K/AKT/GSK3β/mTOR signaling cascades, and SD (12 hr) shared a common etiology consisting of complex bidirectional interactions with SCF.

摘要

本研究旨在探讨睡眠剥夺(SD)与五味子(SCF)治疗在抗抑郁样作用中的相互作用。我们观察到,SD 加重了慢性不可预测轻度应激(CUMS)在高架十字迷宫测试中引起的焦虑样行为。然而,强迫游泳试验和蔗糖偏好试验表明,SD(12 小时)减轻了 CUMS 和 SD 引起的抑郁症状,而 SD(72 小时)则有相反的作用。SCF 给药对 CUMS 和 SD 引起的抑郁和焦虑表现出有希望的治疗效果。此外,根据行为测试,SCF 可能增强了 SD(12 小时)的抗抑郁样作用。此外,SD(12 小时)和 SCF 处理后海马体中的 BDNF 水平升高,并伴随着 TrkB/CREB/ERK 和 PI3K/AKT/GSK3β/mTOR 信号通路的上调。此外,mTOR 的下游靶蛋白 p70S6K 和 PSD95 的蛋白水平也因治疗而增加。这些结果表明,SCF 在 CUMS 中的抗抑郁样作用依赖于 BDNF 的激活以及 TrkB/CREB/ERK 和 PI3K/AKT/GSK3β/mTOR 信号级联的调节,而 SD(12 小时)与 SCF 之间存在复杂的双向相互作用,具有共同的发病机制。

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