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稳胆汤通过调节食欲素-A 和瘦素表达改善睡眠剥夺大鼠的负性情绪。

Wen-dan decoction improves negative emotions in sleep-deprived rats by regulating orexin-a and leptin expression.

机构信息

School of Preclinical Medicine, Beijing University of Chinese Medicine, No. 11 Bei Sanhuan Donglu, Chaoyang District, Beijing 100029, China.

Traditional Chinese Medical Hospital of Ji'nan, Shandong 250012, China.

出版信息

Evid Based Complement Alternat Med. 2014;2014:872547. doi: 10.1155/2014/872547. Epub 2014 Apr 17.

Abstract

Wen-Dan Decoction (WDD), a formula of traditional Chinese medicine, has been clinically used for treating insomnia for approximately 800 years. However, the therapeutic mechanisms of WDD remain unclear. Orexin-A plays a key role in the sleep-wake cycle, while leptin function is opposite to orexin-A. Thus, orexin-A and leptin may be important factors in sleep disorders. In this study, 48 rats were divided into control, model, WDD-treated, and diazepam-treated groups. The model of insomnia was produced by sleep deprivation (SD) for 14 days. The expressions of orexin-A, leptin, and their receptors in blood serum, prefrontal cortex, and hypothalamus were detected by enzyme-linked immunosorbent assay, immunohistochemistry, and real time PCR. Open field tests showed that SD increased both crossing movement (Cm) and rearing-movement (Rm) times. Orexin-A and leptin levels in blood serum increased after SD but decreased in brain compared to the control group. mRNA expressions of orexin receptor 1 and leptin receptor after SD were decreased in the prefrontal cortex but were increased in hypothalamus. WDD treatment normalized the behavior and upregulated orexin-A, leptin, orexin receptor 1 and leptin receptor in brain. The findings suggest that WDD treatment may regulate SD-induced negative emotions by regulating orexin-A and leptin expression.

摘要

文丹汤(WDD)是一种中药方剂,临床上用于治疗失眠已有约 800 年的历史。然而,WDD 的治疗机制尚不清楚。食欲素-A 在睡眠-觉醒周期中起着关键作用,而瘦素的功能与食欲素-A 相反。因此,食欲素-A 和瘦素可能是睡眠障碍的重要因素。在这项研究中,将 48 只大鼠分为对照组、模型组、WDD 治疗组和地西泮治疗组。通过 14 天的睡眠剥夺(SD)制作失眠模型。采用酶联免疫吸附试验、免疫组织化学和实时 PCR 检测血清、前额叶皮层和下丘脑内食欲素-A、瘦素及其受体的表达。旷场试验显示,SD 增加了穿越运动(Cm)和立起运动(Rm)的次数。SD 后血清中食欲素-A 和瘦素水平升高,但与对照组相比,大脑中的含量降低。SD 后前额叶皮层中食欲素受体 1 和瘦素受体的 mRNA 表达降低,但在下丘脑增加。WDD 治疗可使大脑中的行为正常化,并上调食欲素-A、瘦素、食欲素受体 1 和瘦素受体。这些发现表明,WDD 治疗可能通过调节食欲素-A 和瘦素的表达来调节 SD 诱导的负面情绪。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/839a/4016855/a947d1366b25/ECAM2014-872547.001.jpg

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