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在小鼠强迫游泳和悬尾试验中对旋花的抗抑郁样活性进行评估。

Evaluation of the antidepressant-like activity of Convolvulus pluricaulis choisy in the mouse forced swim and tail suspension tests.

作者信息

Dhingra Dinesh, Valecha Rekha

机构信息

Department of Pharmaceutical Sciences, Pharmacology Division, Guru Jambheshwar University of Science and Technology, Hisar, India.

出版信息

Med Sci Monit. 2007 Jul;13(7):BR155-61.

Abstract

BACKGROUND

This study investigates the effect of the petroleum ether, chloroform, and ethyl acetate fractions of the total ethanolic extract of Convolvulus pluricaulis Choisy (Family: Convolvulaceae) on depression in mice.

MATERIAL/METHODS: The petroleum ether (25, 50 mg/kg), chloroform (25, 50, 100 mg/kg), and ethyl acetate (25, 50, 100 mg/kg) fractions were administered orally for 10 successive days to separate groups of Swiss young male albino mice. The effects of the extracts on the mice's immobility periods were assessed in the forced swim test (FST) and tail suspension test (TST). The effects of reserpine (2 mg/kg i.p.), sulpiride (50 mg/kg i.p.), prazosin (62.5 microg/kg i.p.), and p-chlorophenylalanine (100 mg/kg i.p.) on the extracts' antidepressant-like effect in TST was also studied. The extracts' antidepressant-like effect was compared with that of imipramine (15 mg/kg p.o.) and fluoxetine (20 mg/kg p.o.) administered for 10 successive days.

RESULTS

Only the chloroform fraction in doses of 50 and 100 mg/kg significantly reduced the immobility time in both FST and TST. This fraction did not significant effect locomotor activity. Its efficacy was found to be comparable to that of imipramine and fluoxetine administered for 10 successive days. The chloroform fraction reversed reserpine-induced extension of immobility period in FST and TST. Prazosin, sulpiride, and p-chlorophenylalanine significantly attenuated the chloroform fraction-induced antidepressant-like effect in TST.

CONCLUSIONS

The chloroform fraction of the total ethanolic extract of Convolvulus pluricaulis elicited a significant antidepressant-like effect in mice by interaction with the adrenergic, dopaminergic, and serotonergic systems.

摘要

背景

本研究考察了旋花(旋花科)乙醇总提取物的石油醚、氯仿和乙酸乙酯部位对小鼠抑郁的影响。

材料/方法:将石油醚部位(25、50毫克/千克)、氯仿部位(25、50、100毫克/千克)和乙酸乙酯部位(25、50、100毫克/千克)分别连续10天口服给予不同组别的瑞士雄性幼龄白化小鼠。通过强迫游泳试验(FST)和悬尾试验(TST)评估提取物对小鼠不动时间的影响。还研究了利血平(2毫克/千克腹腔注射)、舒必利(50毫克/千克腹腔注射)、哌唑嗪(62.5微克/千克腹腔注射)和对氯苯丙氨酸(100毫克/千克腹腔注射)对提取物在TST中抗抑郁样作用的影响。将提取物的抗抑郁样作用与连续10天给予的丙咪嗪(15毫克/千克口服)和氟西汀(20毫克/千克口服)进行比较。

结果

仅50和100毫克/千克剂量的氯仿部位能显著缩短FST和TST中的不动时间。该部位对运动活性无显著影响。发现其疗效与连续10天给予的丙咪嗪和氟西汀相当。氯仿部位可逆转利血平诱导的FST和TST中不动时间的延长。哌唑嗪、舒必利和对氯苯丙氨酸可显著减弱氯仿部位在TST中诱导的抗抑郁样作用。

结论

旋花乙醇总提取物的氯仿部位通过与肾上腺素能、多巴胺能和5-羟色胺能系统相互作用,在小鼠中产生显著的抗抑郁样作用。

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