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孕酮对胃肠道动力的抑制作用。

Progesterone inhibitory role on gastrointestinal motility.

机构信息

Department of Physiology and Biochemistry, School of Medicine, Jordan University of Science and Technology, Irbid, Jordan.

出版信息

Physiol Res. 2022 Apr 30;71(2):193-198. doi: 10.33549/physiolres.934824. Epub 2022 Mar 28.

DOI:10.33549/physiolres.934824
PMID:35344673
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9150547/
Abstract

Progesterone is a steroidal hormone that is produced from the corpus luteum of the ovaries and from the placenta. The main function of progesterone is to promote the secretory differentiation in the endometrium of the uterus and to maintain pregnancy by inhibiting uterine contractions throughout pregnancy. Progesterone performs its actions by activating the classical progesterone nuclear receptors that affect gene transcription and by the non-classical activation of cell surface membrane receptors that accounts for the rapid actions of progesterone. Besides the reproductive roles of progesterone, it exerts functions in many tissues and systems such as the nervous system, the bone, the vascular system, and the gastrointestinal (GI) tract. This review will summarize the recent literature that investigated the role of progesterone in GI tract motility. Most literature indicates that progesterone exerts an inhibitory role on gut smooth muscle cells in part by elevating nitric oxide synthesis which induces relaxation in smooth muscle. Moreover, progesterone inhibits the signaling pathways that lead to contraction such as Rho kinase inhibition. These data serve as a quick resource for the future directions of progesterone research that could lead to better understanding and more effective treatment of gender-related GI tract motility disorders.

摘要

孕激素是一种甾体激素,由卵巢的黄体和胎盘产生。孕激素的主要功能是促进子宫子宫内膜的分泌分化,并通过抑制整个孕期的子宫收缩来维持妊娠。孕激素通过激活经典的孕激素核受体来发挥作用,这些受体影响基因转录,通过非经典的激活细胞表面膜受体来发挥作用,这解释了孕激素的快速作用。除了孕激素的生殖作用外,它还在许多组织和系统中发挥作用,如神经系统、骨骼、血管系统和胃肠道(GI)道。这篇综述将总结最近研究孕激素在胃肠道动力中的作用的文献。大多数文献表明,孕激素通过增加诱导平滑肌松弛的一氧化氮合成,对肠道平滑肌细胞发挥抑制作用。此外,孕激素抑制导致收缩的信号通路,如 Rho 激酶抑制。这些数据为孕激素研究的未来方向提供了快速资源,这可能导致更好地理解和更有效地治疗与性别相关的胃肠道动力障碍。

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Progesterone inhibitory role on gastrointestinal motility.孕酮对胃肠道动力的抑制作用。
Physiol Res. 2022 Apr 30;71(2):193-198. doi: 10.33549/physiolres.934824. Epub 2022 Mar 28.
2
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本文引用的文献

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Horm Behav. 2021 Jan;127:104873. doi: 10.1016/j.yhbeh.2020.104873. Epub 2020 Oct 19.
2
Progesterone increases blood glucose via hepatic progesterone receptor membrane component 1 under limited or impaired action of insulin.孕激素通过肝孕激素受体膜成分 1 在胰岛素作用有限或受损的情况下增加血糖。
Sci Rep. 2020 Oct 1;10(1):16316. doi: 10.1038/s41598-020-73330-7.
3
The Role Of Progestogens In Threatened And Idiopathic Recurrent Miscarriage.孕激素在先兆流产和特发性复发性流产中的作用
Int J Womens Health. 2019 Nov 7;11:589-596. doi: 10.2147/IJWH.S224159. eCollection 2019.
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Effects of progesterone on glucose uptake in neurons of Alzheimer's disease animals and cell models.孕激素对阿尔茨海默病动物和细胞模型神经元葡萄糖摄取的影响。
Life Sci. 2019 Dec 1;238:116979. doi: 10.1016/j.lfs.2019.116979. Epub 2019 Oct 21.
5
Role of mPRα (PAQR7) in progesterone-induced Ca2+ decrease in human vascular smooth muscle cells.mPRα(PAQR7)在孕激素诱导的人血管平滑肌细胞钙离子减少中的作用。
J Mol Endocrinol. 2019 Oct;63(3):199-213. doi: 10.1530/JME-19-0019.
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Changes in Gastric Smooth Muscle Cell Contraction during Pregnancy: Effect of Estrogen.孕期胃平滑肌细胞收缩的变化:雌激素的作用
J Pregnancy. 2019 Apr 4;2019:4302309. doi: 10.1155/2019/4302309. eCollection 2019.
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Effect of progesterone on nitric oxide/cyclic guanosine monophosphate signaling and contraction in gastric smooth muscle cells.孕酮对胃平滑肌细胞中一氧化氮/环磷酸鸟苷信号传导及收缩的影响。
Biomed Rep. 2018 Dec;9(6):511-516. doi: 10.3892/br.2018.1161. Epub 2018 Oct 18.
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Progesterone and human cognition.孕酮与人类认知。
Climacteric. 2018 Aug;21(4):333-340. doi: 10.1080/13697137.2018.1476484. Epub 2018 Jun 1.
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Horm Behav. 2018 Aug;104:100-110. doi: 10.1016/j.yhbeh.2018.04.013. Epub 2018 May 9.
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Progesterone induces relaxation of human umbilical cord vascular smooth muscle cells through mPRα (PAQR7).孕酮通过 mPRα(PAQR7)诱导人脐带动脉平滑肌细胞松弛。
Mol Cell Endocrinol. 2018 Oct 15;474:20-34. doi: 10.1016/j.mce.2018.02.003. Epub 2018 Feb 9.