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山竹果皮水提物的毒理学评价。

Toxicological assessments of aqueous extract of Eugenia jambolana stem bark.

机构信息

Department of Pharmacology, School of Pharmacy and Technology Management, NMIMS University, Mumbai, India.

出版信息

Pharm Biol. 2010 Aug;48(8):849-54. doi: 10.3109/13880200903300204.

Abstract

Eugenia jambolana Lam. (Myrtaceae) is widely used in folk medicine as an antidiabetic, but there is a lack of information about its toxicity, especially for the stem bark. The present study evaluated acute oral and repeated-dose toxicity of the stem bark aqueous extract of Eugenia jambolana (EJ) in albino mice and Wistar rats. In the acute toxicity tests, mice received oral doses of EJ extract as 300, 2000, and 5000 mg/kg body weight. Mortality, signs of toxicity, body weight, food consumption, and gross findings were observed for 14 days post-treatment. In repeated toxicity, rats were orally treated with 300, 1000, and 2000 mg/kg body weight, and animals were observed till the 28th day of treatment. At the end of the study period, surviving animals were fasted overnight and anesthetized for blood collection and removal of some vital organs for histopathology. No significant differences were noted in body and organ weights between the control and treated groups from either of the studies. In addition, hematological parameters, e.g., red blood cell count (RBC), hemoglobin concentration (Hb), mean corpuscular hemoglobin concentration (MCHC), platelets (PLT), and white blood cell differential count, biochemical parameters, e.g., blood glucose, creatinine, blood urea nitrogen (BUN), alkaline phosphatase (ALP), bilirubin, total protein, and albumin, and ions, e.g., potassium, sodium, chloride, calcium, and phosphorus, were studied in the repeated-dose toxicity study. In conclusion, these investigations indicate the safety of acute and repeated oral administration of the aqueous extract of EJ stem bark, suggesting therefore that it may be continuously used safely.

摘要

罗望子(桃金娘科)在民间医学中被广泛用作抗糖尿病药物,但关于其毒性,特别是茎皮毒性的信息却很少。本研究评估了罗望子茎皮水提物(EJ)在白化小鼠和 Wistar 大鼠中的急性口服和重复剂量毒性。在急性毒性试验中,小鼠口服 EJ 提取物剂量分别为 300、2000 和 5000mg/kg 体重。在治疗后 14 天内观察死亡率、毒性症状、体重、食物消耗和大体观察结果。在重复毒性试验中,大鼠口服给予 300、1000 和 2000mg/kg 体重,观察动物至治疗第 28 天。在研究结束时,存活的动物禁食过夜,并麻醉采集血液和取出一些重要器官进行组织病理学检查。在这两项研究中,与对照组相比,处理组的体重和器官重量均无显著差异。此外,在重复剂量毒性研究中还研究了血液学参数,例如红细胞计数(RBC)、血红蛋白浓度(Hb)、平均红细胞血红蛋白浓度(MCHC)、血小板(PLT)和白细胞分类计数,生化参数,例如血糖、肌酐、血尿素氮(BUN)、碱性磷酸酶(ALP)、胆红素、总蛋白和白蛋白,以及离子,如钾、钠、氯、钙和磷。总之,这些研究表明 EJ 茎皮水提物的急性和重复口服给药是安全的,因此可以安全地连续使用。

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