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哈姆斯茎皮甲醇提取物的安全性评估:Wistar大鼠急性和亚慢性经口毒性研究

Safety assessment of the methanol extract of the stem bark of Harms: Acute and subchronic oral toxicity studies in Wistar rats.

作者信息

Tchoumtchoua Job, Mouchili Oumarou Riepouo, Ateba Sylvin Benjamin, Zingue Stéphane, Halabalaki Maria, Mbanya Jean Claude, Skaltsounis Alexios-Leandros, Njamen Dieudonné

机构信息

Laboratory of Animal Physiology, Department of Animal Biology and Physiology, Faculty of Science, University of Yaounde I, P.O. Box 812, Yaounde, Cameroon.

Division of Pharmacognosy and Natural Products Chemistry, Faculty of Pharmacy, University of Athens, Panepistimioupoli Zografou, 15771, Athens, Greece.

出版信息

Toxicol Rep. 2014 Oct 16;1:877-884. doi: 10.1016/j.toxrep.2014.10.003. eCollection 2014.

Abstract

Harms (Leguminosae) is widely used traditionally in Central and West Africa for the treatment of various ailments. However, no data regarding its safety have been published until now. Thus, the present study aimed to investigate the potential toxicity of the methanol extract of the stem bark of (AP) in Wistar rats following the OECD guidelines. In acute oral toxicity, female rats received a single dose of 2000 mg/kg of AP and were observed for 14 days. In subchronic toxicity, doses of 150, 300, 600 mg/kg/day of AP were given to rats (males and females) for 28 days. No death and abnormal behaviors were observed in acute toxicity and the LD was estimated higher than 5000 mg/kg. In the subchronic study, AP induced no significant variation in body weight and relative weight of organs, whereas a delayed decrease of white blood cell count and granulocytes was observed. Inconsistent increase of the total cholesterol/high density lipoprotein was observed at 600 mg/kg in males. Such variation (not dose dependent) and without biological relevance indicate a wide margin of safety for the traditional use of AP.

摘要

哈姆斯(豆科)在中非和西非传统上被广泛用于治疗各种疾病。然而,迄今为止尚未发表有关其安全性的数据。因此,本研究旨在按照经合组织指南,研究哈姆斯(AP)茎皮甲醇提取物对Wistar大鼠的潜在毒性。在急性经口毒性试验中,雌性大鼠接受单剂量2000 mg/kg的AP,并观察14天。在亚慢性毒性试验中,给大鼠(雄性和雌性)分别给予150、300、600 mg/kg/天的AP,持续28天。在急性毒性试验中未观察到死亡和异常行为,估计半数致死量高于5000 mg/kg。在亚慢性研究中,AP对体重和器官相对重量未引起显著变化,而观察到白细胞计数和粒细胞数量延迟下降。在雄性大鼠中,600 mg/kg剂量时观察到总胆固醇/高密度脂蛋白不一致增加。这种变化(与剂量无关)且无生物学相关性表明,AP传统用途的安全范围很宽。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/977e/5598524/f0883eb8128f/gr1.jpg

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