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通用阿育吠陀药物特里卡图在查尔斯·福斯特大鼠中的安全性评估。

Safety evaluation of Trikatu, a generic Ayurvedic medicine in Charles Foster rats.

作者信息

Chanda Debabrata, Shanker Karuna, Pal Anirban, Luqman Suaib, Bawankule Dnyaneshwar Umrao, Mani Dayanandan, Darokar Mahendra Pandurang

机构信息

Genetic Resources and Biotechnology Division, Central Institute of Medicinal and Aromatic Plants (CSIR).

出版信息

J Toxicol Sci. 2009 Feb;34(1):99-108. doi: 10.2131/jts.34.99.

Abstract

Chemical characterization and acute and sub-acute toxicity study of Trikatu, a generic herbal formulation of Indian system of medicine, was carried out in Charles Foster (CF) rats for safety profiling. In acute toxicity experiment, Trikatu at 2,000 mg/kg body weight once orally was well tolerated by the experimental animals (both male and female) and no changes were observed in mortality, morbidity, gross pathology, gain in weight, vital organ weight, hematological (total white blood cells (WBC) and red blood cells (RBC) count), biochemical parameters such as serum creatinine, serum glutamate oxaloacetate transaminase (SGOT), serum glutamate pyruvate transaminase (SGPT), serum lipid profile and tissue biochemical parameters such as reduced glutathione and malonaldehyde content as oxidative stress markers. In sub-acute experiment, Trikatu was administered at 5, 50 and 300 mg/kg body weight once daily for 28 days in female CF rats, and non-significant changes were found in most of the parameters studied such as acute experiment except significant increase in low density lipoprotein (LDL) cholesterol level at 50 and 300 mg/kg body weight, decrease in high density lipoprotein (HDL) cholesterol level at 300 mg/kg body weight, increase in SGPT activity at 50 mg/kg body weight and decrease in WBC count at 300 mg/kg body weight on 28(th) day post treatment.

摘要

对印度传统医学通用草药配方特里卡图(Trikatu)进行了化学表征以及急性和亚急性毒性研究,以评估其安全性,实验选用了查尔斯·福斯特(CF)大鼠。在急性毒性实验中,实验动物(雄性和雌性)口服一次2000毫克/千克体重的特里卡图后耐受性良好,在死亡率、发病率、大体病理学、体重增加、重要器官重量、血液学指标(白细胞(WBC)和红细胞(RBC)总数)、生化参数如血清肌酐、血清谷草转氨酶(SGOT)、血清谷丙转氨酶(SGPT)、血清脂质谱以及作为氧化应激标志物的组织生化参数如还原型谷胱甘肽和丙二醛含量等方面均未观察到变化。在亚急性实验中,对雌性CF大鼠每日一次给予5、50和300毫克/千克体重的特里卡图,持续28天,结果发现,除了在第28天治疗后,体重50和300毫克/千克组低密度脂蛋白(LDL)胆固醇水平显著升高、300毫克/千克组高密度脂蛋白(HDL)胆固醇水平降低、50毫克/千克组SGPT活性升高以及300毫克/千克组白细胞计数降低外,所研究的大多数参数与急性实验一样没有显著变化。

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