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驱虫斑鸠菊种子提取物的植物化学、卤虫致死性及小鼠急性经口毒性研究

Phytochemistry, Brine shrimp lethality and mice acute oral toxicity studies on seed extracts of Vernonia anthelmintica.

作者信息

Jamil Subia, Khan Rafeeq Alam, Afroz Syeda, Ahmed Shadab

机构信息

Department of Pharmacology, Faculty of Pharmacy and Pharmaceutical Sciences, University of Karachi, Karachi, Pakistan / Faculty of Pharmacy, Jinnah University for Women, Karachi, Pakistan.

Department of Pharmacology, Faculty of Pharmacy and Pharmaceutical Sciences, University of Karachi, Karachi, Pakistan.

出版信息

Pak J Pharm Sci. 2016 Nov;29(6):2053-2057.

Abstract

Despite the widespread use of Vernonia anthelmintica seeds in traditional medicine, the need to establish the safety of the Vernonia anthelmintica is required to ascertain the safe use of this herbal medicine. The aim of the present study is to establish the acute toxicity profile of different extracts of Vernonia anthelmintica. Hexane and ethanol extract of Vernonia Anthelmintica has been studied for its brine shrimp lethality potential. Water decoction (WDVA), Hexane (HEVA) and Ethanol (EEVA) extracts of Vernonia anthelmintica has also been evaluated for their in-vivo acute oral toxicity in mice by Lorke's method. Phytochemistry of all three extracts was also evaluated for the presence of their secondary metabolites. All three extracts showed the presence of flavonoids and terpenoids, while alkaloids, tannins and fixed oils were present in HEVA and EEVA. Furthermore EEVA also showed presence of carbohydrates and HEVA also showed the presence of cardiac glycosides. Ethanol and hexane extracts of Vernonia anthelmintica showed a positive cytotoxicity in brine shrimp lethality test at 24 hours with LC50 104.16 (224.0-48.05)μg/ml and 216.11μg/ml (378.2-128.7) respectively as compared to standard drug etoposide LC50 7.46μg/ml. The oral LD50 for EEVA, HEVA and WDVA in mice by Lorke's method was greater than 5000mg/kg. The result of brine shrimp lethality test clearly exhibited the presence of bioactive compounds with cytotoxic potential; however seems to be safe for oral use since LD50 was higher than 5000mg/kg and thus safety of acute dosing in vivo practices is justified.

摘要

尽管驱虫斑鸠菊种子在传统医学中被广泛使用,但为了确定这种草药的安全使用,仍需要确定驱虫斑鸠菊的安全性。本研究的目的是确定驱虫斑鸠菊不同提取物的急性毒性特征。对驱虫斑鸠菊的己烷和乙醇提取物进行了卤虫致死潜力研究。还通过洛尔科方法评估了驱虫斑鸠菊的水煎剂(WDVA)、己烷提取物(HEVA)和乙醇提取物(EEVA)对小鼠的体内急性经口毒性。还对所有三种提取物的植物化学性质进行了评估,以确定其次级代谢产物的存在。所有三种提取物均显示含有黄酮类化合物和萜类化合物,而HEVA和EEVA中含有生物碱、单宁和固定油。此外,EEVA还显示含有碳水化合物,HEVA还显示含有强心苷。与标准药物依托泊苷的LC50 7.46μg/ml相比,驱虫斑鸠菊的乙醇和己烷提取物在24小时的卤虫致死试验中显示出阳性细胞毒性,LC50分别为104.16(224.0 - 48.05)μg/ml和216.11μg/ml(378.2 - 128.7)。通过洛尔科方法测得EEVA、HEVA和WDVA对小鼠的经口LD50大于5000mg/kg。卤虫致死试验结果清楚地表明存在具有细胞毒性潜力的生物活性化合物;然而,由于LD50高于5000mg/kg,口服似乎是安全的,因此在体内急性给药实践中的安全性是合理的。

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