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姜黄精油的急性和亚慢性毒性以及致突变性评价。

Acute and subchronic toxicity as well as mutagenic evaluation of essential oil from turmeric (Curcuma longa L).

机构信息

Department of Biochemistry, Amala Cancer Research Centre, Amala Nagar 680555, Thrissur, Kerala, India.

出版信息

Food Chem Toxicol. 2013 Mar;53:52-61. doi: 10.1016/j.fct.2012.11.027. Epub 2012 Nov 29.

DOI:10.1016/j.fct.2012.11.027
PMID:23201370
Abstract

The present study investigated the acute, subchronic and genotoxicity of turmeric essential oil (TEO) from Curcuma longa L. Acute administration of TEO was done as single dose up to 5 g of TEO per kg body weight and subchronic toxicity study for thirteen weeks was done by daily oral administration of TEO at doses 0.1, 0.25 and 0.5 g/kg b.wt. in Wistar rats. There were no mortality, adverse clinical signs or changes in body weight; water and food consumption during acute as well as subchronic toxicity studies. Indicators of hepatic function such as aspartate aminotransferase (AST), alanine amino transferase (ALT) and alkaline phosphatase (ALP) were unchanged in treated animals compared to untreated animals. Oral administration of TEO for 13 weeks did not alter total cholesterol, triglycerides, markers of renal function, serum electrolyte parameters and histopathology of tissues. TEO did not produce any mutagenicity to Salmonella typhimurium TA-98, TA-100, TA-102 and TA-1535 with or without metabolic activation. Administration of TEO to rats (1 g/kg b.wt.) for 14 days did not produce any chromosome aberration or micronuclei in rat bone marrow cells and did not produce any DNA damage as seen by comet assay confirming the non toxicity of TEO.

摘要

本研究调查了姜黄精油(TEO)对 Curcuma longa L 的急性、亚慢性和遗传毒性。急性给药采用单剂量,TEO 用量高达 5 克/千克体重,亚慢性毒性研究采用 Wistar 大鼠每日口服 TEO,剂量分别为 0.1、0.25 和 0.5 g/kg bw。在急性和亚慢性毒性研究中,没有动物死亡、出现不良临床症状或体重变化;也没有出现水和食物消耗的变化。与未处理的动物相比,治疗动物的肝功能指标如天冬氨酸氨基转移酶(AST)、丙氨酸氨基转移酶(ALT)和碱性磷酸酶(ALP)没有变化。TEO 连续口服 13 周不会改变总胆固醇、甘油三酯、肾功能标志物、血清电解质参数和组织的组织病理学。TEO 对鼠伤寒沙门氏菌 TA-98、TA-100、TA-102 和 TA-1535 没有产生任何致突变性,无论是否有代谢激活。连续 14 天给大鼠(1 g/kg bw)灌胃 TEO 不会导致大鼠骨髓细胞出现染色体畸变或微核,彗星试验也未显示 DNA 损伤,证实 TEO 没有毒性。

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