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印度银杏中银杏酸共轭物的抗焦虑活性

Anxiolytic activity of ginkgolic acid conjugates from Indian Ginkgo biloba.

作者信息

Satyan K S, Jaiswal A K, Ghosal S, Bhattacharya S K

机构信息

Department of Pharmacology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.

出版信息

Psychopharmacology (Berl). 1998 Mar;136(2):148-52. doi: 10.1007/s002130050550.

Abstract

Ginkgolic acid conjugates (GAC) (6-alkylsalicylates, namely n-tridecyl-, n-pentadecyl-, n-heptadecyl-, n-pentadecenyl- and n-heptadecenylsalicylates) isolated from the leaves of Indian Ginkgo biloba Linn., (IGb) were tested for their putative role in anxiety in rats. Elevated plus maze, open-field behaviour, novelty-induced feeding latency and social interaction were the rodent behavioural models used in this study. GAC (0.3 and 0.6 mg/kg, each, p.o.) on single acute administration, showed dose-related changes in the behaviour. GAC (0.6 mg/kg) and DZ augmented open arm entries, the open arm/closed arm entries ratio and increased time spent in the open arm on the elevated plus maze. In the open field, GAC (0.6 mg/kg) and DZ significantly increased ambulation and reduced the immobility time. EGb 761 showed a similar profile. GAC (0.6 mg/kg) and DZ significantly attenuated the increased latency to feed in novel environment. By contrast, EGb 761 and Ginkocer further augmented feeding latency. None of the drugs tested showed any significant effect in the social interaction test. GAC showed consistent and significant anxiolytic activity in all the variables investigated. By contrast, EGb 761 and Ginkocer, which are devoid of GAC, did not evoke significant activity. However, increased rearing and decreased immobility time only in open field behaviour shown by EGb 761 may be due to some antianxiety activity of a lesser degree. Our observations suggest that GAC may be the active constituents of Ginkgo biloba responsible for the anxiolytic activity.

摘要

从印度银杏叶(IGb)中分离出的银杏酸共轭物(GAC)(6-烷基水杨酸酯,即正十三烷基、正十五烷基、正十七烷基、正十五碳烯基和正十七碳烯基水杨酸酯),对其在大鼠焦虑中的假定作用进行了测试。高架十字迷宫、旷场行为、新奇诱导摄食潜伏期和社交互动是本研究中使用的啮齿动物行为模型。单次急性给予GAC(每次0.3和0.6mg/kg,口服)后,行为出现剂量相关变化。GAC(0.6mg/kg)和地西泮增加了高架十字迷宫中进入开放臂的次数、开放臂/封闭臂进入次数比,并增加了在开放臂上花费的时间。在旷场实验中,GAC(0.6mg/kg)和地西泮显著增加了活动度并减少了不动时间。EGb 761表现出类似的情况。GAC(0.6mg/kg)和地西泮显著减轻了在新环境中摄食潜伏期的增加。相比之下,EGb 761和银杏蜡酯进一步延长了摄食潜伏期。所测试的药物在社交互动测试中均未显示出任何显著效果。GAC在所有研究变量中均表现出一致且显著的抗焦虑活性。相比之下,不含GAC的EGb 761和银杏蜡酯未引发显著活性。然而,EGb 761仅在旷场行为中表现出增加竖毛行为和减少不动时间,这可能归因于某种程度较轻的抗焦虑活性。我们的观察结果表明,GAC可能是银杏中负责抗焦虑活性的活性成分。

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