Analgesic and anti-inflammatory activities of the n-butanol fraction of Vernonia glaberrima

I. Nasir, A. Yusuf, M. Abdullahi, A. Uba, A. Muntaka, S. S. Bello, A. Umar, A. Alhasan, C. Alebiosu, M. Yahaya, Mohammad Shah Hafez Kabir, C. Ottah, S. Ibrahim
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Abstract

The n-butanol leaf fraction of Vernonia glaberrima was evaluated for its toxicity, analgesic and anti-inflammatory effects. The leaves of V. glaberrima were collected, identified and extracted with methanol using maceration method and the resulting crude methanol extract was then partitioned using different solvents of increasing polarity (hexane, chloroform, ethyl acetate and n-butanol respectively). Preliminary phytochemical screening was conducted on the n-butanol fraction (BF) using standard procedures. The median lethal dose (LD50) of the fraction was determined using Lorke’s method and the analgesic effect was evaluated using acetic acid-induced writhing test in mice, while the anti-inflammatory activity was assessed using carrageenan-induced paw oedema in rats. Secondary metabolites including saponins, tannins, alkaloids, glycosides and flavonoids were found in the fraction. The LD50 of the fraction was 2154 mg/kg indicating the fraction to be moderately toxic. The fraction at 150 mg/kg exhibited 77.6 % inhibition of writhes, higher than the standard drug, piroxicam (10 mg/kg) which had 53.7 % inhibition. The n-butanol fraction at 150 and 250 mg/kg significantly inhibited the carrageenan-induced paw oedema at the 2nd and 4th hour, respectively, while there was no significant inhibition at 500 mg/kg of the fraction. The standard drug was only able to inhibit oedema at the 1st hour. The results showed the n-butanol fraction of V. glaberrima to possess significant analgesic and anti-inflammatory activities thereby validating its traditional use in the treatment of pain and inflammation.
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山梨正丁醇部分的镇痛和抗炎作用
研究了光水仙花正丁醇叶提取物的毒性、镇痛和抗炎作用。采用浸渍法对光蓝叶片进行收集、鉴定和甲醇提取,然后用极性递增的不同溶剂(分别为己烷、氯仿、乙酸乙酯和正丁醇)对粗甲醇提取物进行分离。采用标准程序对正丁醇馏分(BF)进行初步植物化学筛选。采用Lorke法测定其中位致死剂量(LD50),采用醋酸致小鼠扭体实验评价其镇痛作用,采用卡拉胶致大鼠足跖水肿实验评价其抗炎作用。次生代谢产物包括皂苷、单宁、生物碱、糖苷和黄酮类化合物。该馏分的LD50为2154 mg/kg,为中毒性。在150 mg/kg浓度下,其对扭体的抑制率为77.6%,高于标准药物吡罗昔康(10 mg/kg)的53.7%。150和250 mg/kg正丁醇组分分别在第2和第4小时显著抑制卡拉胶诱导的足跖水肿,而500 mg/kg正丁醇组分无显著抑制作用。标准药物仅能在第1小时抑制水肿。结果表明,光灰草正丁醇部分具有显著的镇痛和抗炎活性,从而验证了其在治疗疼痛和炎症方面的传统用途。
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