Diallo Aboudoulatif, Eklu-Gadegbeku Kwashie, Amegbor Koffi, Agbonon Amegnona, Aklikokou Kodjo, Creppy Edmond, Gbeassor Messanvi
Department of Toxicology, Faculty of Health Sciences, University of Lome, P.O. Box 216 Lomé 05, Lomé, Togo.
Department of Animal Physiology, Faculty of Sciences, University of Lome, Togo.
J Ethnopharmacol. 2014 Sep 11;155(2):1214-8. doi: 10.1016/j.jep.2014.07.005. Epub 2014 Jul 15.
In African traditional medicine, Ageratum conyzoides has been used as purgative, febrifuge, anti-ulcer and wound dressing. To date there is no safety information about long term use of Ageratum conyzoides which contains pyrrolizidine alkaloids, a class of hepatotoxic and carcinogenic phytochemicals. This study aims to evaluate the 90 days subchronic toxicity and in vitro toxicity of Ageratum conyzoides.
Three groups of 8 rats (4 males and 4 females) received distilled water (control), 500 and 1000 mg/kg of the extract daily for 90 consecutive days by oral gavage. The animals were observed daily for abnormal clinical signs and death. Body weight, relative organ weight, haematological and biochemical parameters of blood as well as heart, kidney, liver and spleen tissues histology were evaluated.
After 90 days administration, Ageratum conyzoides increased significantly (p<0.05) the relative weight of the liver, the spleen and kidney as compared to control group. Ageratum conyzoides increased also significantly (p<0.05) ALP, ALT, AST and blood glucose. Furthermore, an increase in the number of platelets associated with a normocytic and normochromic anaemia was observed. The cytotoxicity, determined by the MTT test and neutral red assay, has shown that the cytotoxicity of hydroalcoholic extract of Ageratum conyzoides and its total alkaloids was very close.
Our results have shown that Ageratum conyzoides at 500 and 1000 mg/kg can induce liver, kidney and haematological disorders. These toxics effects can be attributed to its total alkaloids especially to pyrrolizidine alkaloids which are present in this plant.
在非洲传统医学中,藿香蓟被用作泻药、退烧药、抗溃疡药和伤口敷料。迄今为止,关于长期使用含有吡咯里西啶生物碱(一类具有肝毒性和致癌性的植物化学物质)的藿香蓟,尚无安全信息。本研究旨在评估藿香蓟90天的亚慢性毒性和体外毒性。
三组,每组8只大鼠(4只雄性和4只雌性),连续90天每天通过灌胃给予蒸馏水(对照组)、500和1000 mg/kg的提取物。每天观察动物的异常临床症状和死亡情况。评估体重、相对器官重量、血液的血液学和生化参数以及心脏、肾脏、肝脏和脾脏组织的组织学。
给药90天后,与对照组相比,藿香蓟显著增加了肝脏、脾脏和肾脏的相对重量(p<0.05)。藿香蓟还显著增加了碱性磷酸酶、谷丙转氨酶、谷草转氨酶和血糖(p<0.05)。此外,观察到血小板数量增加,伴有正细胞正色素性贫血。通过MTT试验和中性红试验测定的细胞毒性表明,藿香蓟水醇提取物及其总生物碱的细胞毒性非常接近。
我们的结果表明,500和1000 mg/kg的藿香蓟可引起肝脏、肾脏和血液系统紊乱。这些毒性作用可归因于其总生物碱,尤其是该植物中存在的吡咯里西啶生物碱。