调节褪黑激素受体可调节生殖生理:阿戈美拉汀对大鼠发情周期、妊娠、后代和子宫收缩的影响

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Accounts of Chemical Research Pub Date : 2023-12-31
E Kacar, F Tan, S Sahinturk, G Zorlu, I Serhatlioglu, O Bulmus, Z Ercan, H Kelestimur
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引用次数: 0

摘要

阿戈美拉汀是一种药物化合物,可作为褪黑激素受体的激动剂,对 MT1 和 MT2 受体亚型具有特殊的亲和力。它的作用模式与多种生理过程的调节密不可分,包括昼夜节律的协调、睡眠-觉醒周期和情绪调节。在本研究中,我们深入探讨了阿戈美拉汀与发情周期、妊娠期、后代数量和子宫收缩调节之间错综复杂的相互作用,揭示了它们对生殖生理的共同影响。实验同时进行了体内和体外实验。Wistar Albino 大鼠分为四组:两组非妊娠组(D1 和 D2)和两组妊娠组(G1 和 G2)。D1 和 G1 组为对照组,D2 和 G2 组长期服用阿戈美拉汀(10 毫克/千克)。使用子宫肌层条在体外评估子宫收缩情况。褪黑激素受体拮抗剂卢吲哚(Luzindole)被用来研究阿戈美拉汀对子宫收缩影响的介导途径。在体内研究中,长期服用阿戈美拉汀可延长发情期(p
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modulation of Melatonin Receptors Regulates Reproductive Physiology: The Impact of Agomelatine on the Estrus Cycle, Gestation, Offspring, and Uterine Contractions in Rats.

Agomelatine is a pharmaceutical compound that functions as an agonist for melatonin receptors, with a particular affinity for the MT1 and MT2 receptor subtypes. Its mode of action is integral to the regulation of diverse physiological processes, encompassing the orchestration of circadian rhythms, sleep-wake cycles, and mood modulation. In the present study, we delve into the intricate interplay between agomelatine and the modulation of estrus cycles, gestation periods, offspring numbers, and uterine contractions, shedding light on their collective impact on reproductive physiology. Both in vivo and in vitro experiments were performed. Wistar Albino rats, divided into four groups: two non-pregnant groups (D1 and D2) and two pregnant groups (G1 and G2). The D1 and G1 groups served as control groups, while the D2 and G2 groups received chronic agomelatine administration (10 mg/kg). Uterine contractions were assessed in vitro using myometrial strips. Luzindole, a melatonin receptor antagonist, was employed to investigate the pathway mediating agomelatine's effects on uterine contractions. In in vivo studies, chronic agomelatine administration extended the diestrus phase (p<0.05) in non-pregnant rats, prolonged the gestational period (p<0.01), and increased the fetal count (p<0.01) in pregnant rats. Additionally, agomelatine reduced plasma oxytocin and prostoglandin-E levels (p<0.01) during pregnancy. In vitro experiments showed that agomelatine dose-dependently inhibited spontaneous and oxytocin-induced myometrial contractions. Luzindole (2 µM) reverse the agomelatine-induced inhibition of myometrial contractions. These findings suggest that agomelatine holds the potential to modulate diverse reproductive parameters during the gestational period, influencing estrus cycling, gestational progression, offspring development, and the orchestration of uterine contractions.

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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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