The actions of resveratrol in decidualizing endometrium: acceleration or inhibition?†

蜕膜化 蜕膜细胞 白藜芦醇 蜕膜 子宫内膜 生物 促炎细胞因子 间质细胞 男科 胚胎 内分泌学 内科学 细胞生物学 药理学 免疫学 炎症 怀孕 医学 癌症研究 胎儿 胎盘 遗传学
作者
Keiji Kuroda,Asako Ochiai,Jan J. Brosens
出处
期刊:Biology of Reproduction [Oxford University Press]
卷期号:103 (6): 1152-1156 被引量:16
标识
DOI:10.1093/biolre/ioaa172
摘要

Abstract Resveratrol, a natural polyphenolic compound, is widely studied for its anti-inflammatory and antisenescent properties. Recently, two studies reported seemingly conflicting findings on the actions of resveratrol on decidualization of human endometrial stromal cells (HESCs). One study by Ochiai et al. demonstrated that resveratrol inhibits decidual transformation of primary cultured HESCs. The other study by Mestre Citrinovitz et al., showed that resveratrol enhances decidualization of HESCs in culture. At a glance, the reason for these opposing observations seems puzzling. However, recent studies demonstrated that decidualization is a multistep process, which starts with an acute proinflammatory stress response that lasts for several days and is followed by the emergence of stress-resistant decidual cells as well as senescent decidual cells. The balance between these decidual subpopulations may determine if the cycling endometrium can successfully transition into the decidua of pregnancy upon embryo implantation. Here, we explore the importance of timing of drugs aimed at modulating the decidual response. We posit that resveratrol treatment during the initial proinflammatory decidual phase, i.e., coinciding with the implantation window in vivo, inhibits decidual transformation of the endometrium. However, when given after the initial phase, resveratrol may promote decidualization by inhibiting decidual senescence. Further, if restricted to the proliferative phase, resveratrol may promote ovarian function without adversely impacting on embryo implantation or decidualization. Thus, failure to align drug interventions with the correct phase of the menstrual cycle may negate beneficial clinical effects and results in adverse reproductive outcomes.
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