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导致雄性大鼠生殖毒性的环芹醛的种属特异性代谢:体内和体外评估。

A species specific metabolism leading to male rat reprotoxicity of Cyclamen aldehyde: in vivo and in vitro evaluation.

机构信息

Fragrances S&T, Ingredients Research, Givaudan Schweiz AG, CH-8310 Kemptthal, Switzerland.

Regulatory Affairs & Product Safety Givaudan UK Ltd, UK.

出版信息

Food Chem Toxicol. 2021 Jul;153:112243. doi: 10.1016/j.fct.2021.112243. Epub 2021 Apr 27.

Abstract

Cyclamen aldehyde (CA; 3-(4-isopropylphenyl)-2-methylpropanal) is a widely used fragrance material. Repeated dose studies in rats revealed adverse effects on sperm maturation. Here we review all the mechanistic and in vivo evidence, to determine relevancy to human health. The effect on spermatogenesis appears to be linked to the metabolite p-isopropyl-benzoic acid (p-iPBA). Studies in rat, rabbit and human suspended hepatocytes indicated species differences with p-iPBA detected in rat hepatocytes only. In plated rat hepatocytes, p-iPBA is conjugated to Coenzyme A (CoA) and p-iPBA-CoA accumulates to stable levels over 22 h. In vitro accumulation of CoA conjugates is a metabolic hallmark correlated to male rat reproductive toxicity for related compounds. p-iPBA-CoA is formed in vivo in liver and testes of rats dosed with CA. In plated rabbit and human hepatocytes p-iPBA-CoA doesn't accumulate. Correlating to this lack of metabolite accumulation, no effects of CA on spermatogenesis were observed in a rabbit in vivo study. A species specific metabolic fate linked to CA toxicity in male rats is postulated which appears not relevant to the rabbit as non-responder species. Lack of accumulation of p-iPBA-CoA in human hepatocytes indicates that like rabbits, humans are unlikely to be vulnerable to p-iPBA hepatic and testicular toxicity.

摘要

环青醛(CA;3-(4-异丙基苯基)-2-甲基丙醛)是一种广泛使用的香料材料。在大鼠中的重复剂量研究显示对精子成熟有不良影响。在这里,我们回顾了所有的机制和体内证据,以确定其与人类健康的相关性。对精子发生的影响似乎与代谢物对异丙基苯甲酸(p-iPBA)有关。在大鼠、兔和人悬浮肝细胞中的研究表明,种属差异仅在大鼠肝细胞中检测到 p-iPBA。在贴壁大鼠肝细胞中,p-iPBA 与辅酶 A(CoA)结合,p-iPBA-CoA 在 22 小时内积累到稳定水平。体外 CoA 缀合物的积累是与相关化合物雄性大鼠生殖毒性相关的代谢标志。CA 给药的大鼠肝脏和睾丸中体内形成 p-iPBA-CoA。在贴壁的兔和人肝细胞中,p-iPBA-CoA 不会积累。与这种代谢物积累的缺乏相关,在兔体内研究中未观察到 CA 对精子发生的影响。推测与雄性大鼠 CA 毒性相关的种特异性代谢命运在兔子等非反应物种中并不相关。人肝细胞中 p-iPBA-CoA 的积累缺乏表明,与兔子一样,人类不太可能易患 p-iPBA 肝和睾丸毒性。

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