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越鞠丸迅速诱导抗抑郁样作用,并在小鼠大脑中急性增强脑源性神经营养因子的表达。

Yueju pill rapidly induces antidepressant-like effects and acutely enhances BDNF expression in mouse brain.

机构信息

Center for Translational Systems Biology and Neuroscience, School of Basic Biomedical Science, Nanjing University of Chinese Medicine, Nanjing 210023, China ; Laboratory of Integrative Biomedicine of Brain Diseases, School of Basic Biomedical Science, Nanjing University of Chinese Medicine, Nanjing 210023, China.

出版信息

Evid Based Complement Alternat Med. 2013;2013:184367. doi: 10.1155/2013/184367. Epub 2013 Apr 22.

DOI:10.1155/2013/184367
PMID:23710213
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3654702/
Abstract

The traditional antidepressants have a major disadvantage in delayed onset of efficacy, and the emerging fast-acting antidepressant ketamine has adverse behavioral and neurotoxic effects. Yueju pill, an herb medicine formulated eight hundred years ago by Doctor Zhu Danxi, has been popularly prescribed in China for alleviation of depression-like symptoms. Although several clinical outcome studies reported the relative short onset of antidepressant effects of Yueju, this has not been scientifically investigated. We, therefore, examined the rapid antidepressant effect of Yueju in mice and tested the underlying molecular mechanisms. We found that acute administration of ethanol extract of Yueju rapidly attenuated depressive-like symptoms in learned helpless paradigm, and the antidepressant-like effects were sustained for at least 24 hours in tail suspension test in ICR mice. Additionally, Yueju, like ketamine, rapidly increased the expression of brain-derived neurotrophic factor (BDNF) in the hippocampus, whereas the BDNF mRNA expression remained unaltered. Yueju rapidly reduced the phosphorylation of eukaryotic elongation factor 2 (eEF2), leading to desuppression of BDNF synthesis. Unlike ketamine, both the BDNF expression and eEF2 phosphorylation were revered at 24 hours after Yueju administration. This study is the first to demonstrate the rapid antidepressant effects of an herb medicine, offering an opportunity to improve therapy of depression.

摘要

传统的抗抑郁药在疗效出现时间上存在主要缺点,而新兴的快速作用抗抑郁药氯胺酮则具有不良的行为和神经毒性作用。越鞠丸是由朱丹溪医生在八百年前制定的一种草药,在中国一直被广泛用于缓解抑郁症状。尽管有几项临床结果研究报告了越鞠丸相对较短的抗抑郁作用起效时间,但这尚未得到科学研究。因此,我们在小鼠中检查了越鞠丸的快速抗抑郁作用,并测试了潜在的分子机制。我们发现,越鞠丸的乙醇提取物急性给药可迅速减轻习得性无助范式中的抑郁样症状,并且在 ICR 小鼠的悬尾试验中,抗抑郁样作用至少持续 24 小时。此外,越鞠丸与氯胺酮一样,可迅速增加海马中的脑源性神经营养因子(BDNF)的表达,而 BDNF mRNA 的表达则保持不变。越鞠丸可迅速降低真核延伸因子 2(eEF2)的磷酸化,从而抑制 BDNF 的合成。与氯胺酮不同,在越鞠丸给药后 24 小时,BDNF 的表达和 eEF2 磷酸化均恢复正常。这项研究首次证明了一种草药的快速抗抑郁作用,为改善抑郁症的治疗提供了机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27c0/3654702/71316216974a/ECAM2013-184367.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27c0/3654702/10991bfe7ce9/ECAM2013-184367.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27c0/3654702/4a913e361037/ECAM2013-184367.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27c0/3654702/30f0efaed6aa/ECAM2013-184367.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27c0/3654702/16c2eea0a418/ECAM2013-184367.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27c0/3654702/71316216974a/ECAM2013-184367.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27c0/3654702/10991bfe7ce9/ECAM2013-184367.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27c0/3654702/4a913e361037/ECAM2013-184367.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27c0/3654702/30f0efaed6aa/ECAM2013-184367.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27c0/3654702/16c2eea0a418/ECAM2013-184367.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27c0/3654702/71316216974a/ECAM2013-184367.005.jpg

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