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单萜(百里香酚)对大鼠地西泮诱导的戒断症状的神经保护作用。

Neuroprotective role of a monoterpene (thymol) on diazepam induced withdrawal symptoms in rats.

作者信息

Saleem Sadia, Naqvi Fizza, Batool Asma, Naqvi Sajjad Haider, Naqvi Faizan, Batool Zehra, Tabassum Saiqa, Haider Saida

机构信息

Neurochemistry and Biochemical Neuropharmacology Research Unit, Department of Biochemistry, University of Karachi, Karachi, Pakistan.

Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan.

出版信息

Pak J Pharm Sci. 2021 Jul;34(4(Supplementary)):1615-1620.

Abstract

Benzodiazepine administration is known to be related to tolerance and a withdrawal syndrome on sudden cessation. Thymol possesses multiple biological properties especially in the pathogenesis of different brain disorders. However, to the best of our knowledge there is no study that relates the use of thymol to benzodiazepine induced withdrawal symptoms. Therefore the aim of the current study was to investigate the usefulness of thymol in the treatment of benzodiazepine withdrawal syndrome in rats. Animals were divided into four groups, thymol (40mg/kg/ml), diazepam (4 mg/kg), thymol + diazepam and vehicle control group. The treatment was given for 14 days and then suddenly ceased. After 24 h animals were tested in different behavioral paradigms such as physical signs for withdrawal, marble burying test, inverted screen test, elevated plus maze, passive avoidance test and open field activity. The results of the present study revealed that co-administration of thymol significantly reduced the withdrawal symptoms induced by diazepam. Our results further suggest that administration of thymol not only ameliorates rebound anxiety associated with diazepam withdrawal but also improves motor and memory impairment in rats.

摘要

已知使用苯二氮䓬会产生耐受性,且突然停药会引发戒断综合征。百里香酚具有多种生物学特性,尤其在不同脑部疾病的发病机制方面。然而,据我们所知,尚无研究将百里香酚的使用与苯二氮䓬引起的戒断症状联系起来。因此,本研究的目的是探讨百里香酚在治疗大鼠苯二氮䓬戒断综合征中的效用。将动物分为四组:百里香酚组(40毫克/千克/毫升)、地西泮组(4毫克/千克)、百里香酚+地西泮组和赋形剂对照组。治疗持续14天,然后突然停药。24小时后,对动物进行不同行为模式的测试,如戒断体征、大理石掩埋试验、倒屏试验、高架十字迷宫试验、被动回避试验和旷场活动。本研究结果显示,百里香酚联合使用可显著减轻地西泮引起的戒断症状。我们的结果进一步表明,给予百里香酚不仅可改善与地西泮戒断相关的反弹性焦虑,还可改善大鼠的运动和记忆障碍。

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