Ji Bingyu, Deng Fengying, Zhou Bingqing, Zhao Chenxuan, Lei Jiahui, Xu Ting, Qiu Junlan, Zhang Meihua, Zhang Yueming, Wei Minggang, Gao Qinqin
Institute for Fetology, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Department of Gynecology and Obstetrics, Dushu Lake Hospital Affiliated to Soochow University, Suzhou, Jiangsu, 215100, People's Republic of China.
Cell Mol Life Sci. 2024 Dec 24;82(1):12. doi: 10.1007/s00018-024-05549-w.
Maternal western-style diets that are high in glucose and fat have well-known cardiovascular effects on offspring, yet the combined influence of such diets during pregnancy is relatively less comprehended. This study investigates the impact of maternal high glucose and fat diet (HGF) on vascular constriction in offspring and the underlying mechanisms.
Pregnant Sprague-Dawley rats were provided with either HGF or control diets. The assessment of fetal and postnatal vascular function disclosed an enhanced sensitivity to angiotensin II-induced vascular constriction in the offspring exposed to HGF. This was ascribed to increased oxidative stress via upregulated NOX2 expression, which was due to downregulated SHIP2 expression that was influenced by upregulated miR-325-3p. The maternal HGF diet elevated miR-325-3p, suppressed SHIP2 and enhanced NOX2 expression in fetal vascular tissues, thereby resulting in vascular dysfunction. These alterations persist into adulthood, heightening the risk of vascular diseases.
The present study is the first to demonstrate that maternal HGF diet impairs vascular constriction function in offspring through the miR-325-3p/SHIP2/NOX2 pathway. These novel findings indicate that the detrimental effects of maternal HGF diet on fetal vascular function can persist into adulthood, advancing our knowledge on the impact of maternal diet on offspring vascular health and the early stages of fetal-origin vascular diseases.
富含葡萄糖和脂肪的西式孕妇饮食对后代心血管系统的影响已为人熟知,然而孕期此类饮食的综合影响相对了解较少。本研究调查母体高糖高脂饮食(HGF)对后代血管收缩的影响及其潜在机制。
给怀孕的斯普拉格-道利大鼠喂食HGF或对照饮食。对胎儿和出生后血管功能的评估显示,暴露于HGF的后代对血管紧张素II诱导的血管收缩敏感性增强。这归因于通过上调NOX2表达导致氧化应激增加,而这是由于受上调的miR-325-3p影响SHIP2表达下调所致。母体HGF饮食使胎儿血管组织中miR-325-3p升高,SHIP2受到抑制,NOX2表达增强,从而导致血管功能障碍。这些改变持续到成年期,增加了血管疾病的风险。
本研究首次证明母体HGF饮食通过miR-325-3p/SHIP2/NOX2途径损害后代的血管收缩功能。这些新发现表明,母体HGF饮食对胎儿血管功能的有害影响可延续至成年期,增进了我们对母体饮食对后代血管健康及胎儿源性血管疾病早期阶段影响的认识。