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苦巴旦杏仁油(Mart.)在小鼠体内的急性和亚急性(28 天)口服毒性研究。

Acute and subacute (28 days) oral toxicity studies of tucum almond oil ( Mart.) in mice.

机构信息

Postgraduate Program in Health and Development in the Midwest Region, Medical School, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.

Faculty of Pharmaceutical Sciences, Food and Nutrition, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.

出版信息

Drug Chem Toxicol. 2022 Jul;45(4):1754-1760. doi: 10.1080/01480545.2021.1871737. Epub 2021 Jan 13.

Abstract

Oils extracted from almonds are often used with particular interest due to their prospective health effects and benefits. Tucum is a Pantanal fruit widely consumed by local population and no toxicity studies regarding its safety are available in the literature to date. This study investigated the acute and subacute toxicity of tucum almond oil (TAO) in mice by evaluating its safety profile. For the acute (2000 mg/kg) and subacute (250, 500 and 1000 mg/kg) toxicity studies, TAO was administered orally to mice according to 425 and 407 Organization for Economic Cooperation and Development Guidelines, respectively. Food intake, body, and organ weight of animals were recorded. Signs of toxicity were assessed, and hematological, biochemical and histopathological analyses were performed. In the acute toxicity study, no mortality or behavioral changes were observed in mice treated with 2000 mg/kg, indicating that LD50 is higher than this dose. In the subacute toxicity test, the doses evaluated did not produce relevant changes in hematological, biochemical or histopathological parameters in the exposed animals. The data obtained suggest that TAO did not induce toxicity after exposure to a single or repeated doses and LD50 value may be considered to be more than 2000 mg/kg body weight.

摘要

杏仁油由于其潜在的健康影响和益处而受到特别关注。图库姆是一种广泛存在于潘塔纳尔地区并被当地居民食用的水果,目前文献中尚无关于其安全性的毒理学研究。本研究通过评估其安全性特征,调查了图库姆杏仁油(TAO)在小鼠中的急性和亚急性毒性。在急性(2000mg/kg)和亚急性(250、500 和 1000mg/kg)毒性研究中,根据经济合作与发展组织的 425 和 407 号指南,分别经口给予 TAO 小鼠。记录动物的食物摄入量、体重和器官重量。评估毒性症状,并进行血液学、生物化学和组织病理学分析。在急性毒性研究中,用 2000mg/kg 处理的小鼠未观察到死亡率或行为改变,表明 LD50 高于该剂量。在亚急性毒性试验中,所评估的剂量未在暴露动物的血液学、生物化学或组织病理学参数中产生相关变化。所得数据表明,TAO 在单次或重复剂量暴露后未引起毒性,LD50 值可能超过 2000mg/kg 体重。

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