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脑与血浆中 carbaryl 水平和胆碱酯酶抑制的关系。

Relationship between brain and plasma carbaryl levels and cholinesterase inhibition.

机构信息

Neurotoxicology Branch, Toxicity Assessment Division, National Health and Environmental Effects Research Laboratory, Office of Research and Development, U.S. EPA, Research Triangle Park, NC 27711, United States.

出版信息

Toxicology. 2010 Oct 29;276(3):172-83. doi: 10.1016/j.tox.2010.08.001. Epub 2010 Aug 11.

Abstract

Carbaryl is a N-methylcarbamate pesticide and, like others in this class, is a reversible inhibitor of cholinesterase (ChE) enzymes. Although studied for many years, there is a surprising lack of information relating tissue levels of carbaryl with ChE activity in the same animals. The present studies were undertaken to describe the dose-response relationship about 40 min (approximate time of maximal ChE inhibition) after oral treatment in adult, post-natal day (PND) 17, and PND11 rats. Additionally, the time-course of plasma ChE activity and carbaryl levels in adult rats was determined after a 30 mg/kg dosage of carbaryl. The time-course study found that carbaryl levels could be detected in plasma 1 h after dosing, but rapidly decreased below the level of quantitation by the 2 h time point. In the dose-response studies, treatment-related increases in plasma and brain carbaryl levels were observed 40 min after dosing. Plasma levels of carbaryl increased linearly, while brain levels appeared to asymptote after 75 mg/kg carbaryl. Plasma and brain levels of carbaryl appeared to be linearly related with a slope close to 1 after various dosages (range: 1-75 mg/kg) of carbaryl at the 40 min time point. Finally, the dose-related relationship between tissue levels of carbaryl and ChE activity was described using a first order exponential decay function with an asymptote. The parameters of this function did not appear to differ between adult, PND17, or PND11 rats. This indicates that age-related differences in brain ChE inhibition by carbaryl are unlikely to be the result of greater tissue levels of the pesticide in PND11 animals. These are the first studies to report the relationship between brain and plasma tissue levels of carbaryl and ChE activity on an individual animal basis. The results of these experiments will be useful to extend physiologically-based pharmacokinetic models for carbaryl and their application in risk assessment.

摘要

carbaryl 是一种 N-甲基氨基甲酸酯类农药,与该类别的其他农药一样,它是胆碱酯酶 (ChE) 酶的可逆抑制剂。尽管已经研究了多年,但关于在同一动物中 carbaryl 的组织水平与 ChE 活性之间的关系,仍存在惊人的信息缺乏。本研究旨在描述成年、出生后第 17 天 (PND17) 和 PND11 大鼠口服治疗后约 40 分钟 (ChE 抑制的大致时间) 时的剂量反应关系。此外,还确定了成年大鼠给予 carbaryl 30mg/kg 剂量后血浆 ChE 活性和 carbaryl 水平的时间过程。时间过程研究发现,carbaryl 水平在给药后 1 小时即可在血浆中检测到,但在 2 小时时间点迅速降至定量水平以下。在剂量反应研究中,在给药后 40 分钟观察到与治疗相关的血浆和大脑 carbaryl 水平升高。血浆 carbaryl 水平呈线性增加,而脑水平在给予 75mg/kg carbaryl 后似乎达到平台。在各种剂量 (范围:1-75mg/kg) 下,在 40 分钟时间点,血浆和脑 carbaryl 水平与 ChE 活性呈线性相关,斜率接近 1。最后,使用一阶指数衰减函数和渐近线描述了组织中 carbaryl 水平与 ChE 活性之间的剂量相关关系。该函数的参数在成年、PND17 或 PND11 大鼠之间似乎没有差异。这表明 carbaryl 对大脑 ChE 抑制的年龄相关差异不太可能是 PND11 动物中该农药组织水平较高的结果。这些是首次在单个动物基础上报告 carbaryl 的大脑和血浆组织水平与 ChE 活性之间关系的研究。这些实验的结果将有助于扩展 carbaryl 的基于生理学的药代动力学模型及其在风险评估中的应用。

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