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甜叶悬钩子水醇提物的急毒和亚急毒研究。

Acute and sub-acute toxicity study of hydroalcoholic fruit extract of Pithecellobium dulce.

机构信息

Research and Development Centre, Bharathiar University, Coimbatore 641046, India.

出版信息

Nat Prod Res. 2012;26(12):1167-71. doi: 10.1080/14786419.2011.562206. Epub 2011 Oct 24.

Abstract

This study was carried out to evaluate the acute and sub-acute toxicity profile of the hydroalcoholic fruit extract (HAEPD) of Pithecellobium dulce (Leguminosae). Albino rats were treated orally with 100, 200 and 500 mg kg(-1) bodyweight (BW) of HAEPD for 90 days to assess its sub-acute toxicity. HAEPD at single doses of 100, 500, 1000, 2000 and 4000 mg kg(-1) BW was also administered to rats to assess its acute toxicity. The rats were observed for physical discomfort, BW change and feeding habits. Pithecellobium dulce did not cause any abnormal changes in haematological or biochemical parameters. Pathologically, no gross abnormality in the tissue architecture was observed. The LD(50) was found to be 3916 mg kg(-1) BW and potential effective doses for efficacy studies are 100 and 300 mg kg(-1) BW as the minimum and maximum doses, respectively. It is concluded that HAEPD can be used safely for experimental and clinical trials.

摘要

本研究旨在评估苦甜水黄皮(豆科)水醇果提取物(HAEPD)的急性和亚急性毒性概况。用 100、200 和 500mg/kg 体重(BW)的 HAEPD 对白化大鼠进行口服处理 90 天,以评估其亚急性毒性。还对大鼠单次给予 HAEPD 100、500、1000、2000 和 4000mg/kg BW,以评估其急性毒性。观察大鼠的身体不适、BW 变化和饮食习惯。苦甜水黄皮未引起血液学或生物化学参数的任何异常变化。组织学上未观察到明显的大体异常。LD(50) 为 3916mg/kg BW,有效剂量为 100 和 300mg/kg BW,分别为最小和最大剂量。结论是 HAEPD 可安全用于实验和临床试验。

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