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逍遥散对慢性不可预测轻度应激大鼠抑郁样行为的影响:神经甾体及其合成和代谢酶。

Effects of Refined Xiaoyaosan on Depressive-Like Behaviors in Rats with Chronic Unpredictable Mild Stress through Neurosteroids, Their Synthesis and Metabolic Enzymes.

机构信息

School of Basic Medical Science, Beijing University of Chinese Medicine, Beijing 100029, China.

Beijing Fengtai District Fangzhuang Community Health Service Center, Beijing 100078, China.

出版信息

Molecules. 2017 Aug 21;22(8):1386. doi: 10.3390/molecules22081386.


DOI:10.3390/molecules22081386
PMID:28825678
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6152155/
Abstract

t To observe the effects of refined Xiaoyaosan (XYS) on the depressive-like behaviors in rats with chronic unpredictable mild stress (CUMS), and to explore the relationship between the changes of neurosteroids and mRNA expressions of their synthesis and metabolic enzymes, and the mechanism of XYS in the treatment of depression. : Eighty-four healthy male Sprague-Dawley rats were randomly divided into normal group, model group, XYS group and fluoxetine group. The latter three groups were subjected to 21 days of CUMS to prepare the stress depression model. Rats in the XYS group, and fluoxetine group were given intragastric administration with refined XYS and fluoxetine, respectively. The behavioral changes of the rats were observed after 21 days. The contents of pregnenolone (PREG), progesterone (PROG) and alloprognanolone (ALLO) in the plasma of rats were measured by ELISA. The levels of PREG, PROG and ALLO in the hippocampus and amygdala tissues were measured by LC-MS/MS. The mRNA expressions of 3α-hydroxysteroid dehydrogenase (3α-HSD), 3β-hydroxysteroid dehydrogenase (3β-HSD), cholesterol side-chain cleavage enzyme (P450scc) and 5α-reductase (5a-R) in the hippocampus and amygdala were detected by RT-qPCR methods. : There were changes in the model rats. The contents of PREG, PROG and ALLO changed similarly, which reflected in the decrease of PROG and ALLO, and the increase of PREG. The mRNA expression of P450scc was increased, and the mRNA expressions of 3α-HSD, 3β-HSD and 5a-R were decreased. Refined XYS could improve the behaviors of rats and the biological indicators. : There is a neurosteroid dysfunction in the brain region of depression rat model animals, and the mechanism of refined XYS depression treatment may be related to the regulation of the control of mRNA expression of related synthesis and metabolic enzymes in the hippocampus and amygdala, further affecting the contents of neurosteroids.

摘要

观察加味逍遥散对慢性不可预知轻度应激(CUMS)大鼠抑郁样行为的影响,探讨神经甾体变化及其合成和代谢酶的 mRNA 表达变化与加味逍遥散治疗抑郁症的关系机制。方法:将 84 只健康雄性 Sprague-Dawley 大鼠随机分为正常组、模型组、加味逍遥散组和氟西汀组。后 3 组采用 21 天 CUMS 制备应激抑郁模型。加味逍遥散组和氟西汀组分别给予灌胃加味逍遥散和氟西汀。21 天后观察大鼠行为变化。采用 ELISA 法检测大鼠血浆中 pregnenolone(PREG)、progesterone(PROG)和 alloprognanolone(ALLO)的含量。采用 LC-MS/MS 法检测海马和杏仁核组织中 PREG、PROG 和 ALLO 的含量。采用 RT-qPCR 法检测海马和杏仁核组织中 3α-羟甾脱氢酶(3α-HSD)、3β-羟甾脱氢酶(3β-HSD)、胆固醇侧链裂解酶(P450scc)和 5α-还原酶(5a-R)的 mRNA 表达。结果:模型大鼠行为发生改变,PREG、PROG 和 ALLO 含量变化趋势一致,表现为 PROG 和 ALLO 降低,PREG 升高。P450sccmRNA 表达增加,3α-HSD、3β-HSD 和 5a-RmRNA 表达降低。加味逍遥散可改善大鼠行为及生物学指标。结论:抑郁模型动物脑区存在神经甾体功能障碍,加味逍遥散治疗抑郁症的机制可能与其调控海马和杏仁核相关合成及代谢酶的 mRNA 表达有关,进而影响神经甾体含量有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6397/6152155/957e236fd336/molecules-22-01386-g008a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6397/6152155/2ddf29f488e3/molecules-22-01386-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6397/6152155/3848efc0f00b/molecules-22-01386-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6397/6152155/59cda219e603/molecules-22-01386-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6397/6152155/c9bbe6a3872d/molecules-22-01386-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6397/6152155/fb0dd589781d/molecules-22-01386-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6397/6152155/583d16103da2/molecules-22-01386-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6397/6152155/957e236fd336/molecules-22-01386-g008a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6397/6152155/2ddf29f488e3/molecules-22-01386-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6397/6152155/8acd2be513f2/molecules-22-01386-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6397/6152155/3848efc0f00b/molecules-22-01386-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6397/6152155/59cda219e603/molecules-22-01386-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6397/6152155/c9bbe6a3872d/molecules-22-01386-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6397/6152155/fb0dd589781d/molecules-22-01386-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6397/6152155/583d16103da2/molecules-22-01386-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6397/6152155/957e236fd336/molecules-22-01386-g008a.jpg

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本文引用的文献

[1]
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J Ethnopharmacol. 2011-5-26

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Biol Psychiatry. 2010-7-23

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