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孕酮对于预防 LPS 诱导的妊娠丢失至关重要。LIF 作为孕酮抗炎作用的潜在介质。

Progesterone is essential for protecting against LPS-induced pregnancy loss. LIF as a potential mediator of the anti-inflammatory effect of progesterone.

机构信息

Centro de Estudios Farmacológicos y Botánicos (CONICET-UBA), Buenos Aires, Argentina.

出版信息

PLoS One. 2013;8(2):e56161. doi: 10.1371/journal.pone.0056161. Epub 2013 Feb 7.

Abstract

Lipopolysaccharide (LPS) administration to mice on day 7 of gestation led to 100% embryonic resorption after 24 h. In this model, nitric oxide is fundamental for the resorption process. Progesterone may be responsible, at least in part, for a Th2 switch in the feto-maternal interface, inducing active immune tolerance against fetal antigens. Th2 cells promote the development of T cells, producing leukemia inhibitory factor (LIF), which seems to be important due to its immunomodulatory action during early pregnancy. Our aim was to evaluate the involvement of progesterone in the mechanism of LPS-induced embryonic resorption, and whether LIF can mediate hormonal action. Using in vivo and in vitro models, we provide evidence that circulating progesterone is an important component of the process by which infection causes embryonic resorption in mice. Also, LIF seems to be a mediator of the progesterone effect under inflammatory conditions. We found that serum progesterone fell to very low levels after 24 h of LPS exposure. Moreover, progesterone supplementation prevented embryonic resorption and LPS-induced increase of uterine nitric oxide levels in vivo. Results show that LPS diminished the expression of the nuclear progesterone receptor in the uterus after 6 and 12 h of treatment. We investigated the expression of LIF in uterine tissue from pregnant mice and found that progesterone up-regulates LIF mRNA expression in vitro. We observed that LIF was able to modulate the levels of nitric oxide induced by LPS in vitro, suggesting that it could be a potential mediator of the inflammatory action of progesterone. Our observations support the view that progesterone plays a critical role in a successful pregnancy as an anti-inflammatory agent, and that it could have possible therapeutic applications in the prevention of early reproductive failure associated with inflammatory disorders.

摘要

妊娠第 7 天给小鼠注射脂多糖(LPS)后,24 小时后胚胎吸收率达到 100%。在这种模型中,一氧化氮(NO)是胚胎吸收过程的基础。孕激素可能至少部分地通过在胎-母体界面诱导 Th2 转换,诱导针对胎儿抗原的主动免疫耐受,从而发挥作用。Th2 细胞促进 T 细胞的发育,产生白血病抑制因子(LIF),由于其在早孕期间的免疫调节作用,LIF 似乎很重要。我们的目的是评估孕激素在 LPS 诱导的胚胎吸收机制中的作用,以及 LIF 是否可以介导激素作用。使用体内和体外模型,我们提供的证据表明,循环孕激素是感染引起小鼠胚胎吸收的机制中的一个重要组成部分。此外,LIF 似乎是炎症条件下孕激素作用的介质。我们发现,LPS 暴露 24 小时后,血清孕激素水平降至非常低的水平。此外,孕激素补充预防了胚胎吸收和 LPS 诱导的体内子宫一氧化氮水平升高。结果表明,LPS 在处理 6 和 12 小时后降低了子宫中核孕激素受体的表达。我们研究了妊娠小鼠子宫组织中 LIF 的表达,发现孕激素在体外上调 LIF mRNA 的表达。我们观察到 LIF 能够调节 LPS 在体外诱导的一氧化氮水平,表明它可能是孕激素炎症作用的潜在介质。我们的观察结果支持孕激素作为抗炎剂在成功妊娠中起关键作用的观点,并且它可能在预防与炎症紊乱相关的早期生殖失败方面具有潜在的治疗应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e112/3567061/28ffa772c946/pone.0056161.g001.jpg

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