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首页> 外文期刊>Journal of Ethnopharmacology: An Interdisciplinary Journal Devoted to Bioscientific Research on Indigenous Drugs >Acute and subchronic oral toxicities of Pu-erh black tea extract in Sprague-Dawley rats.
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Acute and subchronic oral toxicities of Pu-erh black tea extract in Sprague-Dawley rats.

机译:普-红茶提取物对Sprague-Dawley大鼠的急性和亚慢性口腔毒性。

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ETHNOPHARMACOLOGICAL RELEVANCE: Pu-erh black tea, which is obtained by first parching crude green tea leaves and then undergoes secondary fermentation with microorganisms, has been believed to be beneficial beverages for health for nearly 2000 years in China, Japan and Taiwan area. But its potential toxicity when administered at a high dose as concentrated extracts has not been completely investigated. THE AIM OF THE STUDY: The present study was aimed at evaluating potential toxicity of Pu-erh black tea extracts (BTE) from acute and sub-chronic administration to male and female Sprague-Dawley (SD) rats. MATERIALS AND METHODS: A single BTE dose of 10,000 mg/kg of body weight was administered by oral gavage for acute toxicity in SD rats. Four groups (10 males and 10 females per group) of dose levels of 1250, 2500, and 5,000 mg/kg/day of the test article, as well as controls (distilled water) were tested as the subchronic toxicity study. RESULTS: No deaths and signs of toxicity occurred during the 14 days of the study. There were no test article related mortalities, body weight gain, feed consumption, clinical observation, organ weight changes, gross finding, clinical or histopathological alterations during the 91-day administration. CONCLUSIONS: The LD(50) of BTE can be defined as more than 10,000 mg/kg, and a dose of 5,000 mg/kg/day was identified as the no-observed-adverse-effect-level (NOAEL) in this study.
机译:人种药理关系:普-红茶是通过先将粗制绿茶干后再与微生物进行二次发酵而制得的,在中国,日本和台湾地区已有近2000年被认为是有益健康的饮料。但是,当以浓缩提取物高剂量给药时,其潜在的毒性尚未完全研究。研究的目的:本研究旨在评估急性和亚慢性给药的普-红茶提取物(BTE)对雄性和雌性Sprague-Dawley(SD)大鼠的潜在毒性。材料与方法:通过口服强饲法给予10,000 mg / kg体重的BTE单剂量,以减轻SD大鼠的急性毒性。作为亚慢性毒性研究,测试了剂量水平为1250、2500和5,000 mg / kg /天的四组(每组10位男性和10位女性)以及对照(蒸馏水)。结果:在研究的14天内没有死亡和毒性迹象的发生。在91天服用期间,没有与测试物品有关的死亡率,体重增加,饲料消耗,临床观察,器官重量变化,总体发现,临床或组织病理学改变。结论:本研究中BTE的LD(50)可以定义为10,000毫克/千克以上,5,000毫克/千克/天的剂量被确定为未观察到的不良反应水平(NOAEL)。

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