Reduced Cystathionine g-Lyase and Increased miR-21 Expression Are Associated with Increased Vascular Resistance in Growth-Restricted Pregnancies Hydrogen Sulfide as a Placental Vasodilator
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Cindrova Davies, Tereza
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Reduced Cystathionine g-Lyase and Increased miR-21 Expression Are Associated with Increased Vascular Resistance in Growth-Restricted Pregnancies Hydrogen Sulfide as a Placental Vasodilator
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Abstract
Increased vascular impedance in the fetoplacental circulation is associated with fetal hypoxia and growth
restriction. We sought to investigate the role of hydrogen sulfide (H2S) in regulating vasomotor tone in the
fetoplacental vasculature. H2S is produced endogenously by catalytic activity of cystathionine b-synthase
and cystathionine g-lyase (CSE). Immunohistochemical analysis localized CSE to smooth muscle cells
encircling arteries in stem villi. Immunoreactivity was reduced in placentas from pregnancies with severe
early-onset growth-restriction and preeclampsia displaying abnormal umbilical artery Doppler waveforms
compared with preeclamptic placentas with normal waveforms and controls. These findings were confirmed
at the protein and mRNA levels. MicroRNA-21, which negatively regulates CSE expression, was increased in
placentas with abnormal Doppler waveforms. Exposure of villus explants to hypoxia-reoxygenation
significantly reduced CSE protein and mRNA and increased microRNA-21 expression. No changes were
observed in cystathionine b-synthase expression, immunolocalized principally to the trophoblast, in
pathologic placentas or in vitro. Finally, perfusion of normal placentas with an H2S donor, after preconstriction
with a thromboxane mimetic, resulted in dose-dependent vasorelaxation. Glibenclamide and
NG-nitro-L-arginine methyl ester partially blocked the effect, indicating that H2S acts through
ATP-sensitive Kþ channels and nitric oxide synthesis. These results demonstrate that H2S is a powerful
vasodilator of the placental vasculature and that expression of CSE is reduced in placentas associated
with increased vascular resistance.
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URI: https://repositorio.uchile.cl/handle/2250/126441
DOI: doi 10.1016/ j.ajpath.2013.01.001
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(Am J Pathol 2013, 182: 1448e1458
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