首页> 美国卫生研究院文献>Evidence-based Complementary and Alternative Medicine : eCAM >Xiangshao Granule Exerts Antidepressive Effects in a Depression Mouse Model by Ameliorating Deficits in Hippocampal BDNF and TrkB
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Xiangshao Granule Exerts Antidepressive Effects in a Depression Mouse Model by Ameliorating Deficits in Hippocampal BDNF and TrkB

机译:香少颗粒通过减轻海马BDNF和TrkB的缺乏而在抑郁症小鼠模型中发挥抗抑郁作用

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摘要

This study explores the therapeutic effects of Xiangshao granules in a mouse depression model and examines the potential molecular mechanisms involved. After 21 consecutive days of chronic stress challenge, all mice were divided into three groups: control group, depression group, and Xiangshao granule treatment group. On the 22nd day, rats in the Xiangshao granule treatment group received Xiangshao granules via gastrogavage for 3 consecutive weeks. Depression group mice showed a significant reduction of crossings (P < 0.01) but not rearings (P < 0.05). Serum CRH, CORT, and ACTH levels were significantly increased in depression mice compared with control (P < 0.05) and the expression levels of hippocampal BDNF and TrkB were reduced in the model group (P < 0.05). However, Xiangshao granule treatment remarkably rescued the decrease in the body weight (P < 0.05), increased crossings in the open field test (P < 0.05), upregulated the expression of hippocampal BDNF and TrkB expression, and reduced the serum CRH, CORT, and ACTH concentrations compared with the depression group (P < 0.05). Collectively, these results demonstrated that Xiangshao granule could effectively induce antidepressive effects in the depression mouse model by ameliorating the expression of hippocampal BDNF and TrkB.
机译:这项研究探讨了香少颗粒在小鼠抑郁症模型中的治疗作用,并研究了其中涉及的潜在分子机制。连续21天的慢性应激挑战后,将所有小鼠分为三组:对照组,抑郁症组和香烧颗粒治疗组。第22天,香the颗粒治疗组大鼠连续3周通过胃管灌胃香received颗粒。抑郁组小鼠的穿越次数显着减少(P <0.01),但未出现饲养(P <0.05)。与对照组相比,抑郁症小鼠的血清CRH,CORT和ACTH水平显着升高(P <0.05),模型组海马BDNF和TrkB的表达水平降低(P <0.05)。然而,香韶颗粒治疗可明显减轻体重的减轻(P <0.05),在野外试验中增加交叉次数(P <0.05),上调海马BDNF和TrkB的表达,并降低血清CRH,CORT,和ACTH浓度与抑郁症组比较(P <0.05)。总的来说,这些结果表明,香参颗粒可以通过改善海马BDNF和TrkB的表达而有效地诱导抑郁症小鼠模型的抗抑郁作用。

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