Analgesic and anti-inflammatory activity of ?-sitosterol isolated from leaves of Oxalis corniculata

S. Dighe, B. Kuchekar, S. Wankhede
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引用次数: 16

Abstract

Oxalis corniculata Linn. (Oxalidaceae) is one of the important medicinal plants used traditionally for the treatment of fever, pain and inflammation. To validate folk use of Oxalis corniculata as analgesic and anti-inflammatory remedy. The leaves of Oxalis corniculata was used for successive extraction with increasing polarity solvents. Petroleum ether extract was selected for activity guided fractionation to isolate ?-sitosterol due to its better efficacy than other extracts. Analgesic activity was done by hot plate test and acetic acid-induced writhings, while anti-inflammatory activity by carrageenan-induced paw edema method. All the extracts were screened at the dose of 100 mg/kg, i.p. and isolated ?-sitosterol was screened at the doses of 5, 10 and 20 mg/kg, i.p. Naloxone (1 mg/kg, s.c.) was used to understand the mechanism of nociception. In hot plate test, Petroleum ether extract was found most active with reaction time of 8.4 0.4 sec after 60 min while isolated ?-sitosterol at dose of 20 mg/kg showed 11.1 0.3 sec after 90 min. The number of writings in 30 min was compared with paracetamol. Petroleum ether extract and ?-sitosterol (20 mg/kg) showed 43.14 1.9 and 34.21 1.4 writhings respectively. Isolated ?-sitosterol (20 mg/kg) inhibited rat paw edema to 0.32 0.06 ml after 120 min. Naloxone reversed antinociceptive effects of extracts and isolated ?-sitosterol. It can be concluded that isolated ?-sitosterol is responsible for analgesic and anti-inflammatory activity of Oxalis corniculata leaves and it works through central mechanism.
牛膝草叶片中-谷甾醇的镇痛和抗炎活性
酢浆草;是传统上用于治疗发烧、疼痛和炎症的重要药用植物之一。目的:验证牛膝草在民间的镇痛抗炎作用。以酢浆草叶为原料,用极性渐强的溶剂进行连续提取。选择石油醚萃取物进行活性引导分离-谷甾醇,其萃取效果优于其他萃取物。采用热板法和醋酸扭体法测定镇痛活性,采用角叉菜胶诱导足跖水肿法测定抗炎活性。所有提取物在100mg /kg, i.p.的剂量下进行筛选,分离的谷甾醇在5mg /kg, i.p.的剂量下进行筛选。纳洛酮(1mg /kg, s.c)用于了解伤害感觉的机制。热板实验中,石油醚提取物的活性最强,60 min后反应时间为8.4 0.4秒,而分离的谷甾醇在20 mg/kg剂量下,90 min后反应时间为11.1 0.3秒。30 min内的写数与对乙酰氨基酚进行比较。石油醚提取物和-谷甾醇(20 mg/kg)的扭曲度分别为43.14 1.9和34.21 1.4。分离-谷甾醇(20 mg/kg)在120 min后可抑制大鼠足部水肿至0.32 0.06 ml。纳洛酮可逆转提取液和分离-谷甾醇的抗痛感作用。由此可见,分离的-谷甾醇参与了草叶的镇痛和抗炎作用,并通过中枢机制发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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