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Investigation of repeated dose (90 day) oral toxicity reproductive/developmental toxicity and mutagenic potential of ‘Calebin A’

机译:研究 Calebin A的重复剂量(90天)的口服毒性生殖/发育毒性和致突变性

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摘要

The present work investigated repeated dose and reproductive toxicity of Calebin A in Wistar rats. A study for assessing the mutagenic potential of Calebin A through an AMES test is also described. Calebin A was orally administered to groups of 10 male and/or 10 female Wistar rats each, assigned to three dose levels (20, 50 and 100 mg/kg/body weight) once daily for 90 consecutive days. None of the animals in any of the treatment/control groups exhibited any abnormal clinical signs/behavioral changes, reproductive as well as developmental parameters, or gross and microscopic changes in both male and female rats. Calebin A was also evaluated for its ability to induce reverse mutations at selected loci of Salmonella typhimurium in the presence and absence of Aroclor 1254 induced rat liver S9 cell lines. In conclusion, 100 mg/kg/d of Calebin A is not likely to produce any significant toxic effects in male and female Wistar rats and no reproductive or developmental toxicity was observed at the same dose and hence Calebin A at 100 mg/kg was determined as “No Observed Adverse Effect Level (NOAEL)” under the test conditions.
机译:目前的工作调查了Calebin A在Wistar大鼠中的重复剂量和生殖毒性。还描述了一项通过AMES测试评估Calebin A诱变潜力的研究。将Calebin A口服给予每组10只雄性和/或10只雌性Wistar大鼠,每组连续3天每天分配三种剂量水平(20、50和100 mg / kg /体重)。在任何治疗/对照组中,在雄性和雌性大鼠中,没有动物表现出任何异常的临床体征/行为变化,生殖和发育参数,或总体和微观变化。在存在和不存在Aroclor 1254诱导的大鼠肝S9细胞系的情况下,还评估了Calebin A在鼠伤寒沙门氏菌的选定基因座上诱导反向突变的能力。总之,100 mg / kg / d的Calebin A在雄性和雌性Wistar大鼠中不太可能产生任何明显的毒性作用,并且在相同剂量下未观察到生殖或发育毒性,因此确定了100 mg / kg的Calebin A在测试条件下为“未观察到不利影响水平(NOAEL)”。

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