首页> 美国卫生研究院文献>Evidence-based Complementary and Alternative Medicine : eCAM >Xiao Yao San Improves Depressive-Like Behavior in Rats through Modulation ofβ-Arrestin 2-Mediated Pathways in Hippocampus
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Xiao Yao San Improves Depressive-Like Behavior in Rats through Modulation ofβ-Arrestin 2-Mediated Pathways in Hippocampus

机译:逍遥散通过调节大鼠抑郁样行为β-arrestin2介导的海马途径

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摘要

Xiao Yao San (XYS) is a classical Chinese medicine formula that has been widely used to treat mood disorders for hundreds of years. To confirm the effect of XYS and better understand its underlying mechanism, high-performance liquid chromatography-mass spectrometry analysis-based quality control of XYS extracts and proteomics-based identification of differential proteins in the hippocampus were adopted in social isolation and chronic unpredictable mild stress- (CUMS-) treated rats. The depressive-like behavior of rats induced by CUMS resembled the manifestation of human depression. The upregulated corticosterone (CORT) and urocortin 2 (UCN2) levels demonstrated the existence of hypothalamic-pituitary-adrenal (HPA) axis hyperactivity. XYS was effective in ameliorating the depressive-like behavior and downregulating UCN2 and CORT. XYS decreased the expression of serine/threonine-protein phosphatase 2A subunit B and increased the expression of β-arrestin 2. The expressions of brain-derived neurotrophic factor (BDNF), tyrosine receptor kinase B (TrkB), and mammalian target of rapamycin (mTOR) were also elevated by XYS. In conclusion, XYS improves social isolation and CUMS-induced depressive-like behavior and ameliorates HPA hyperactivation through the downregulation of corticotrophin releasing hormone (CRH) receptor 2. The upregulation of BDNF/TrkB and the phosphorylation of mTOR require β-arrestin 2 as a scaffold to regulate stress signaling.
机译:逍遥散(XYS)是一种经典的中药配方,数百年来已广泛用于治疗情绪障碍。为了确认XYS的效果并更好地了解其潜在机理,在社会隔离和慢性不可预测的轻度应激中采用了基于高效液相色谱-质谱分析的XYS提取物质量控制和基于蛋白质组学的海马差异蛋白鉴定。 -(CUMS-)处理的大鼠。 CUMS诱导的大鼠的抑郁样行为类似于人类抑郁的表现。上皮皮质激素(CORT)和尿皮质素2(UCN2)的水平升高表明存在下丘脑-垂体-肾上腺(HPA)轴亢进。 XYS可有效改善抑郁症的行为并下调UCN2和CORT。 XYS降低了丝氨酸/苏氨酸蛋白磷酸酶2A亚基B的表达,并增加了β-arrestin2的表达。脑源性神经营养因子(BDNF),酪氨酸受体激酶B(TrkB)和哺乳动物雷帕霉素靶标的表达( XYS也提高了mTOR)。总之,XYS通过下调促肾上腺皮质激素释放激素(CRH)受体2来改善社交隔离和CUMS诱导的抑郁样行为,并改善HPA过度活化。BDNF/ TrkB的上调和mTOR的磷酸化需要β-arrestin2作为支架调节应激信号。

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