啮齿动物发情周期模式:协调周期评价与解释。

IF 3 4区 医学 Q1 MEDICINE, LEGAL
Shivakumar Holalagoudar, Susan Kisielewski, Austin Martini, Kamin Johnson, Anne-Laure Leoni, Corinna Demminger, Sonja Brosel
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引用次数: 0

摘要

从内分泌干扰物的角度来看,发情周期是一个敏感的终点,也包括在啮齿动物生殖毒性研究中。本文综述了动物发情周期计时的方法,以及检测实验室评估动物发情周期天数的不同方法。在计算4天的发情周期时,没有发现重大差异。然而,当发情期延长时,不同检测实验室的周期计数不同,可能导致误解和不准确的结果。在发情周期中出现两到三个E的延长发作需要解释。因此,我们提出以下建议:1)遵循OECD关于正常4/5天周期的指导文件;2)建议更新OECD文件,因为在目前的OECD文件中,对于以发情期(P)结束的5天周期,并伴有发情期(E)的情况没有明确规定;3)在5天周期中,P后出现2次E发作,以及连续3次E发作应被视为异常。4)在第一个周期的第一个E之前或在最后一个周期的最后一个E(5天内的最后一个P)之后的阶段不应被认为是一个完整的周期。此外,还呼吁进行协作,以协调循环计数方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rodent estrous cycle pattern: Harmonizing the cycle evaluation and interpretation.

The estrous cycle is a sensitive endpoint from an endocrine disruptor perspective and is included in rodent reproductive toxicity studies. In this paper, the methods for estrous cycle timing and different approaches followed by testing laboratories for evaluating the days of the estrous cycle were reviewed. No major differences are identified for counting 4-day estrous cycle. However, when extended episodes of estrus (E) stages occur, the cycle counting differs between testing laboratories potentially resulting in misinterpretation and inaccurate outcome. Appearance of extended episodes of two to three E in an estrous cycle need explanation. Therefore, the following are proposed, 1) follow OECD guidance document for normal 4/5 day cycles, 2) recommends an update of the OECD document as in the current one it is unclear for a 5-day cycle ending with Proestrus(P) followed by episode(s) of estrus(E), 3) two episodes of E after P in a 5-day cycle and three consecutive episodes of E should be considered abnormal, and 4) stages prior to first E of the first cycle or after last E (last P of a 5-day) of last cycle should not be assumed a complete cycle. Additionally, call for collaboration is made to harmonize the cycle counting approach.

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来源期刊
CiteScore
6.70
自引率
8.80%
发文量
147
审稿时长
58 days
期刊介绍: Regulatory Toxicology and Pharmacology publishes peer reviewed articles that involve the generation, evaluation, and interpretation of experimental animal and human data that are of direct importance and relevance for regulatory authorities with respect to toxicological and pharmacological regulations in society. All peer-reviewed articles that are published should be devoted to improve the protection of human health and environment. Reviews and discussions are welcomed that address legal and/or regulatory decisions with respect to risk assessment and management of toxicological and pharmacological compounds on a scientific basis. It addresses an international readership of scientists, risk assessors and managers, and other professionals active in the field of human and environmental health. Types of peer-reviewed articles published: -Original research articles of relevance for regulatory aspects covering aspects including, but not limited to: 1.Factors influencing human sensitivity 2.Exposure science related to risk assessment 3.Alternative toxicological test methods 4.Frameworks for evaluation and integration of data in regulatory evaluations 5.Harmonization across regulatory agencies 6.Read-across methods and evaluations -Contemporary Reviews on policy related Research issues -Letters to the Editor -Guest Editorials (by Invitation)
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