Magnesium Sulfate-Mediated Vascular Relaxation and Calcium Channel Activity in Placental Vessels Different From Nonplacental Vessels.

BACKGROUND

Magnesium sulfate (MgSO) has been used as a common therapy for preeclampsia and eclampsia for many years. MgSO decreases peripheral vascular resistance so as to reduce maternal blood pressure. Whether placental blood vessels react to MgSO in the same patterns as that in maternal vessels is largely unknown.

METHODS AND RESULTS

This study compared placental vessels (PV) versus nonplacental vessels (non-PV) in human and animal models. MgSO-caused vascular dilation was significantly weaker in PV than that in non-PV. Prostaglandin I synthetase affected MgSO-mediated vasodilatation in PV, not in umbilical vessels, while cyclooxygenase did not influence MgSO-induced relaxation in both PV and non-PV. Mg-caused vasodilatation was mainly through calcium channels. In PV, calcium channel activities were significantly weaker in PV than that in non-PV. Relative mRNA expression of , , and was significantly higher in PV than those in umbilical vessels, despite the fact that the expression of was less in PV. The contractile phenotype of smooth muscle cell marker (CALD1) was less and the synthetic phenotype (MYH10) was more in PV than that in UV.

CONCLUSIONS

These results demonstrated that PV were characterized by much weaker responses to MgSO compared with nonplacental vessels. The difference was related to weaker calcium channel activity and minor contractile phenotype smooth muscle cells in PV, providing important information for further understanding treatments with MgSO in preeclampsia.