Maternal Supplementation of Inositols, Fucoxanthin, and Hydroxytyrosol in Pregnant Murine Models of Hypertension

伊诺斯 内分泌学 羟基酪醇 内科学 医学 血压 内皮功能障碍 一氧化氮 一氧化氮合酶 生物化学 化学 抗氧化剂 多酚
作者
Daniela Menichini,Mesk Alrais,Liu Chen,Yang Xia,Sean C. Blackwell,Fabio Facchinetti,Baha M. Sibai,Monica Longo
出处
期刊:American Journal of Hypertension [Oxford University Press]
卷期号:33 (7): 652-659 被引量:9
标识
DOI:10.1093/ajh/hpaa041
摘要

Abstract Background Myoinositol (M) and D-chiro-inositol (D) are insulin sensitizer compounds, while fucoxanthin (F) and hydroxytyrosol (H) are antioxidant substances. We aim to investigate if the combination of these compounds, will improve the vascular responses in pregnant mouse models of hypertension: a genetic model, transgenic heterozygous mice lacking endothelial nitric oxide synthase gene (eNOS−/+); and environmental, wild-type (WT) mice. Those mouse models will allow a better understanding of the genetic/environmental contribution to hypertension in pregnancy. Methods eNOS−/+ and WT female were fed high fat diet for 4 weeks, then at 7–8 weeks of age were mated with WT male. On gestational day (GD) 1, they were randomly allocated to receive MDFH treatment or water as control: eNOS−/+ MDFH (n = 13), eNOS−/+ (n = 13), WT-MDFH (n = 14), and WT (n = 20). Systolic blood pressure (SBP) was obtained at GD 18, then dams were sacrificed; fetuses and placentas collected, and 2 mm segments of carotid arteries isolated for vascular responses using the wire-myograph system. Responses to phenylephrine (PE), with/without the NOS inhibitor (N-nitro-l-arginine methyl ester (l-NAME)), and to acetylcholine (Ach) and sodium nitroprussiate (SNP) were performed. Results SBP decreased in eNOS−/+ and WT dams after MDFH supplementation. In eNOS−/+, MDFH lower the contractile response to PE and l-NAME and improved Ach vasorelaxation. In WT dams, MDFH treatment did not affect PE response; MDFH treatment lowered the vascular PE response after incubation with l-NAME. No differences were seen in SNP relaxation in both models. Conclusions MDFH decreased SBP in both genetically and environmentally hypertensive dams and improved vascular responses mostly in the eNOS−/+ dams.
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