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The Regulation of Endothelin-1 in Pregnancies Complicated by Gestational Diabetes: Uncovering the Vascular Effects of Insulin.

Bianca R FatoSally BeardNatalie K BinderNatasha L PritchardTu'uhevaha J Kaitu'u-LinoNatasha De AlwisNatalie J Hannan
Published in: Biomedicines (2023)
Gestational diabetes mellitus (GDM) is a condition of pregnancy defined by new-onset hyperglycemia. GDM is associated with impaired maternal endothelial and vascular reactivity. Endothelin-1 (ET-1) is a potent vasoconstrictor that contributes to endothelial dysfunction, however, its abundance and actions in GDM are unclear. Maternal plasma was obtained from pregnancies complicated by GDM ( n = 24) and gestation-matched controls ( n = 42); circulating ET-1 levels were assessed by ELISA. Human omental arteries from healthy pregnancies and those complicated by GDM were dissected from omental fat biopsies and collected at cesarean section. mRNA expression of ET-1 and its receptors, ET A and ET B , in addition to vascular cell adhesion molecule-1 (VCAM1) and intercellular adhesion molecule-1 (ICAM1) were assessed by qPCR ( n = 28). Using wire myography, we investigated vascular constriction to ET-1 (10 -11 -10 -4 M) in omental arteries from pregnancies complicated by GDM, compared to gestation-matched controls ( n = 7). GDM cases were stratified by clinical management, diet intervention ( n = 5), or insulin treatment ( n = 6). Additionally, arteries from healthy pregnancies were treated with insulin (1 mU/mL ( n = 7) and 10 mU/mL ( n = 5)) or vehicle control. Vasoactive response to ET-1 was measured via wire myography. Circulating ET-1 levels and mRNA expression of the ET-1 system in omental arteries were not found to be significantly different between pregnancies complicated by GDM compared to healthy controls. However, we found insulin treatment during pregnancy and in ex vivo models reduced ET-1 vasoconstriction of maternal vasculature in GDM. These data suggest insulin may improve vascular function in GDM, however, further investigation is needed to define the role of ET-1 in pregnancy.
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