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孕周和胎儿甲状腺功能减退会改变猪的甲状腺以及局部肝脏和肾脏的肾素-血管紧张素系统。

Gestational age and fetal hypothyroidism Alter the porcine thyroid and local hepatic and renal renin-angiotensin systems.

作者信息

Smith Alyssa A, Pasternak J Alex

机构信息

Department of Animal Sciences, Purdue University, West Lafayette, Indiana, USA.

Department of Animal and Food Sciences, University of Kentucky, Lexington, Kentucky, USA.

出版信息

Physiol Rep. 2025 Sep;13(17):e70565. doi: 10.14814/phy2.70565.

Abstract

This study was conducted to examine the ontogeny of and interactions between the thyroid system and local renin-angiotensin systems (RAS) in the porcine fetus. N = 24 pregnant gilts were split into two groups, receiving either a daily dose of methimazole to induce fetal hypothyroidism, or a daily sham control. Within each group, treatment of n = 3 gilts was initiated at gestational day 34, 45, 55, or 65, and terminated 21 days later to allow for fetal sample collection. The morphology of the fetal thyroid was assessed via lectin staining, showing that follicular structure changes with both increasing gestational age and altered thyroid status. Subsequently, the ontogeny of thyroid and RAS-related genes in the fetal liver and kidney, as well as the effect of fetal hypothyroidism, was assessed via qPCR. In the liver, SERPINA7, TTR, THRA, and THRB were all ontogenically regulated, with THRB also ontogenically regulated in the kidney. All studied RAS genes were ontogenically regulated in at least one of the studied tissues. Hypothyroidism caused temporal dysregulations in the expression of hepatic SERPINA7, AGT, ACE, ACE2, and AGTR2, as well as renal THRB, ACE, and AGTR1. These results suggest a temporal and tissue-dependent relationship between the thyroid and RAS in the fetal pig.

摘要

本研究旨在探讨猪胎儿甲状腺系统与局部肾素-血管紧张素系统(RAS)的个体发育及其相互作用。将24头妊娠母猪分为两组,一组每日给予甲巯咪唑以诱导胎儿甲状腺功能减退,另一组为每日假手术对照。在每组中,对n = 3头母猪在妊娠第34、45、55或65天开始治疗,并在21天后终止,以便采集胎儿样本。通过凝集素染色评估胎儿甲状腺的形态,结果显示滤泡结构随胎龄增加和甲状腺状态改变而变化。随后,通过qPCR评估胎儿肝脏和肾脏中甲状腺及RAS相关基因的个体发育,以及胎儿甲状腺功能减退的影响。在肝脏中,SERPINA7、TTR、THRA和THRB均受到个体发育调控,THRB在肾脏中也受到个体发育调控。所有研究的RAS基因在至少一种研究组织中受到个体发育调控。甲状腺功能减退导致肝脏中SERPINA7、AGT、ACE、ACE2和AGTR2以及肾脏中THRB、ACE和AGTR1的表达出现暂时失调。这些结果表明,胎儿猪的甲状腺与RAS之间存在时间和组织依赖性关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d451/12431595/607fcd593b83/PHY2-13-e70565-g003.jpg

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