绵羊早产儿皮质醇浓度升高会影响心脏发育。

IF 2.8 4区 医学 Q2 PHYSIOLOGY
Reza Amanollahi, Stacey L Holman, Melanie R Bertossa, Ashley S Meakin, Vicki L Clifton, Kent L Thornburg, I Caroline McMillen, Michael D Wiese, Mitchell C Lock, Janna L Morrison
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引用次数: 0

摘要

皮质醇的前期升高促进心脏发育和成熟。在这里,我们研究了妊娠中后期循环皮质醇升高对胎羊心脏生长和代谢的影响。生理盐水或皮质醇(2-3 mg, 4.4 mL/24 h)于妊娠109 ~ 116天(孕龄= 150天)注入胎儿颈静脉,116天采集胎儿心脏组织。测定胎儿左心室(LV)组织糖皮质激素浓度、基因及蛋白表达。胎儿内注射皮质醇增加了心脏皮质醇浓度,但降低了糖皮质激素受体(GR)异构体(GRα- a、GR- p、GR- a、GRα- d2和GRα- d3)的蛋白丰度。皮质醇输注可下调心脏增生性生长标志物(IGF1、IGF-1R、TGFβ和AGT)的基因和蛋白表达,上调DNA复制蛋白标志物(增殖细胞核抗原)的表达。心脏蛋白和/或电子传递链复合体I、SOD2、GLUT-4(基因和蛋白)以及磷酸化IRS-1的基因表达随着胎儿皮质醇浓度升高而上调。胎儿皮质醇输注下调PDK4基因表达,PDK4介导从葡萄糖到脂肪酸代谢的代谢转换。皮质醇组参与心血管保护的分子标记(SIRT-1、HO1、LAMP1和SK1)的心脏表达也下调。总之,这些发现表明,早产儿长期暴露于皮质醇会改变心脏发育,促进心脏成熟,如果这些变化持续到成年期,可能会增加以后患心血管疾病的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Elevated cortisol concentration in preterm sheep fetuses impacts heart development.

The prepartum rise in cortisol promotes cardiac development and maturation. Here, we investigated the impact of elevated circulating cortisol during mid-late gestation on cardiac growth and metabolism in fetal sheep. Saline or cortisol (2-3 mg in 4.4 mL/24 h) was infused into the fetal jugular vein from 109 to 116 days gestation (dG, term = 150 dG), and fetal heart tissue was collected at 116 dG. Glucocorticoid concentrations, gene and protein expression were measured in fetal left ventricle (LV) tissue. Intrafetal cortisol infusion increased cardiac cortisol concentration but downregulated the protein abundance of glucocorticoid receptor (GR) isoforms (GRα-A, GR-P, GR-A, GRα-D2 and GRα-D3). The gene and protein expression of markers of cardiac hyperplastic growth (IGF1, IGF-1R, TGFβ and AGT) were downregulated, while a protein marker of DNA replication (proliferating cell nuclear antigen) was upregulated by cortisol infusion. Cardiac protein and/or gene expression of complex I of the electron transport chain, SOD2, GLUT-4 (gene and protein), and phosphorylated IRS-1, were upregulated in response to elevated fetal cortisol concentration. Intrafetal cortisol infusion downregulated gene expression of PDK4, which mediates the metabolic switch from glucose to fatty acid metabolism. Cardiac expression of molecular markers involved in cardiovascular protection (SIRT-1, HO1, LAMP1 and SK1) were also downregulated in the cortisol group. In conclusion, these findings suggest that chronic cortisol exposure in preterm fetuses alters heart development, promoting cardiac maturation and potentially increasing the risk of cardiovascular disease later in life if these changes persist into adulthood.

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来源期刊
Experimental Physiology
Experimental Physiology 医学-生理学
CiteScore
5.10
自引率
3.70%
发文量
262
审稿时长
1 months
期刊介绍: Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged. Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.
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