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红木树叶的初步药理筛选

Preliminary pharmacological screening of Bixa orellana L. leaves.

作者信息

Shilpi Jamil Ahmad, Taufiq-Ur-Rahman Md, Uddin Shaikh Jamal, Alam Md Shahanur, Sadhu Samir Kumar, Seidel Véronique

机构信息

Phytochemistry Research Laboratories, Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, 27 Taylor Street, Glasgow G4 0NR, UK.

出版信息

J Ethnopharmacol. 2006 Nov 24;108(2):264-71. doi: 10.1016/j.jep.2006.05.008. Epub 2006 Jun 12.

Abstract

Preliminary pharmacological studies were performed on the methanol extract of Bixa orellana L. (Bixaceae) leaves to investigate neuropharmacological, anticonvulsant, analgesic, antidiarrhoeal activity and effect on gastrointestinal motility. All studies were conducted in mice using doses of 125, 250 and 500 mg/kg of body weight. In the pentobarbitone-induced hypnosis test, the extract statistically reduced the time for the onset of sleep at 500 mg/kg dose and (dose-dependently) increased the total sleeping time at 250 and 500 mg/kg dose. A statistically significant decrease in locomotor activity was observed at all doses in the open-field and hole-cross tests. In the strychnine-induced anticonvulsant test, the extract increased the average survival time of the test animals (statistically significant at 250 and 500 mg/kg). The extract significantly and dose-dependently reduced the writhing reflex in the acetic acid-induced writhing test. Antidiarrhoeal activity was supported by a statistically significant decrease in the total number of stools (including wet stools) in castor oil-induced diarrhoea model. A statistically significant delay in the passage of charcoal meal was observed at 500 mg/kg in the gastrointestinal motility test. The extract was further evaluated in vitro for antioxidant and antibacterial activity. It revealed radical scavenging properties in the DPPH assay (IC(50)=22.36 microg/ml) and antibacterial activity against selected causative agents of diarrhoea and dysentery, including Shigella dysenteriae.

摘要

对红木(紫葳科)叶的甲醇提取物进行了初步药理研究,以考察其神经药理学、抗惊厥、镇痛、止泻活性及对胃肠动力的影响。所有研究均在小鼠身上进行,使用的剂量为125、250和500毫克/千克体重。在戊巴比妥诱导的催眠试验中,该提取物在500毫克/千克剂量时能显著缩短入睡时间,在250和500毫克/千克剂量时能(剂量依赖性地)延长总睡眠时间。在旷场试验和穿洞试验中,所有剂量下均观察到运动活性显著降低。在士的宁诱导的抗惊厥试验中,该提取物能延长试验动物的平均存活时间(在250和500毫克/千克时具有统计学显著性)。在醋酸诱导的扭体试验中,该提取物能显著且剂量依赖性地减少扭体反射。在蓖麻油诱导的腹泻模型中,粪便(包括稀便)总数显著减少,支持了其止泻活性。在胃肠动力试验中,500毫克/千克剂量时观察到炭末推进显著延迟。该提取物还进行了体外抗氧化和抗菌活性评估。在DPPH试验中显示出自由基清除特性(IC(50)=22.36微克/毫升),并对包括痢疾志贺菌在内的腹泻和痢疾的选定病原体具有抗菌活性。

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