Meems Laura M G, Mahmud Hasan, Buikema Hendrik, Tost Jörg, Michel Sven, Takens Janny, Verkaik-Schakel Rikst N, Vreeswijk-Baudoin Inge, Mateo-Leach Irene V, van der Harst Pim, Plösch Torsten, de Boer Rudolf A
Department of Cardiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Am J Physiol Heart Circ Physiol. 2016 Dec 1;311(6):H1459-H1469. doi: 10.1152/ajpheart.00141.2016. Epub 2016 Oct 21.
Vitamin D deficiency is one of the most common nutritional deficiencies worldwide. Maternal vitamin D deficiency is associated with increased susceptibility to hypertension in offspring, but the reasons for this remain unknown. The aim of this study was to determine if parental vitamin D deficiency leads to altered DNA methylation in offspring that may relate to hypertension. Male and female Sprague-Dawley rats were fed a standard or vitamin D-depleted diet. After 10 wk, nonsibling rats were mated. The conceived pups received standard chow. We observed an increased systolic and diastolic blood pressure in the offspring from depleted parents (F1-depl). Genome-wide methylation analyses in offspring identified hypermethylation of the promoter region of the Pannexin-1 (Panx1) gene in F1-depl rats. Panx1 encodes a hemichannel known to be involved in endothelial-dependent relaxation, and we demonstrated that in F1-depl rats the increase in blood pressure was associated with impaired endothelial relaxation of the large vessels, suggesting an underlying biological mechanism of increased blood pressure in children from parents with vitamin deficiency. Parental vitamin D deficiency is associated with epigenetic changes and increased blood pressure levels in offspring.
维生素D缺乏是全球最常见的营养缺乏症之一。母体维生素D缺乏与后代患高血压的易感性增加有关,但其原因尚不清楚。本研究的目的是确定父母维生素D缺乏是否会导致后代DNA甲基化改变,而这可能与高血压有关。将雄性和雌性Sprague-Dawley大鼠喂以标准饮食或维生素D缺乏饮食。10周后,非同胞大鼠进行交配。受孕的幼崽给予标准食物。我们观察到来自维生素D缺乏父母的后代(F1-缺乏组)收缩压和舒张压升高。对后代进行全基因组甲基化分析发现,F1-缺乏组大鼠中泛连接蛋白-1(Panx1)基因启动子区域存在高甲基化。Panx1编码一种已知参与内皮依赖性舒张的半通道,我们证明在F1-缺乏组大鼠中,血压升高与大血管内皮舒张功能受损有关,这表明维生素缺乏父母的孩子血压升高存在潜在的生物学机制。父母维生素D缺乏与后代的表观遗传变化和血压水平升高有关。