Department of Physiology and Pharmacology, Libin Cardiovascular Institute of Alberta, Calgary, AB T2N 4N1, Canada.
Children's Hospital Research Institute; University of Calgary, Calgary, AB T2N 4N1, Canada.
Int J Mol Sci. 2018 Nov 20;19(11):3665. doi: 10.3390/ijms19113665.
With the rising global tide of obesity, gestational diabetes mellitus (GDM) burgeoned into one of the most common antenatal disorders worldwide. Macrosomic babies born to diabetic mothers are more likely to develop risk factors for cardiovascular disease (CVD) before they reach adulthood. Rodent studies in offspring born to hyperglycemic pregnancies show vascular dysfunction characterized by impaired nitric oxide (NO)-mediated vasodilation and increased production of contractile prostanoids by cyclooxygenase 2 (COX-2). Vascular dysfunction is a key pathogenic event in the progression of diabetes-related vascular disease, primarily attributable to glucotoxicity. Therefore, glucose-induced vascular injury may stem directly from the hyperglycemic intrauterine environment of GDM pregnancy, as evinced by studies showing endothelial activation and inflammation at birth or in childhood in offspring born to GDM mothers. This review discusses potential mechanisms by which intrauterine hyperglycemia programs dysfunction in the developing vasculature.
随着全球肥胖率的上升,妊娠糖尿病(GDM)成为全球最常见的产前疾病之一。患有糖尿病的母亲所生的巨大儿婴儿在成年前更有可能出现心血管疾病(CVD)的风险因素。高血糖妊娠所生后代的啮齿动物研究表明,血管功能障碍的特征是一氧化氮(NO)介导的血管舒张受损和环氧化酶 2(COX-2)产生的收缩性前列腺素增加。血管功能障碍是糖尿病相关血管疾病进展的关键致病事件,主要归因于糖毒性。因此,葡萄糖引起的血管损伤可能直接源自 GDM 妊娠的高血糖宫内环境,这一点可以通过研究在 GDM 母亲所生后代出生时或儿童期显示内皮激活和炎症来证明。这篇综述讨论了宫内高血糖使发育中血管功能障碍程序化的潜在机制。