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Changes in calcium channel proteins according to magnesium sulfate administration in placentas from pregnancies with pre-eclampsia or fetal growth restriction.

Authors :
Hyun-Hwa Cha
Jae-Ryoung Hwang
Ji Hee Sung
Suk-Joo Choi
Soo-young Oh
Cheong-Rae Roh
Cha, Hyun-Hwa
Hwang, Jae-Ryoung
Sung, Ji Hee
Choi, Suk-Joo
Oh, Soo-Young
Roh, Cheong-Rae
Source :
Journal of Investigative Medicine (Sage Publications Inc.); Feb2019, Vol. 67 Issue 2, p319-326, 8p
Publication Year :
2019

Abstract

We aimed to evaluate the changes in plasma membrane Ca2+-ATPase (PMCA) and sarcoendoplasmic reticulum CA2+-ATPase (SERCA-2) according to the antepartal magnesium sulfate (MgSO4) administration in the placentas from pregnancies with pre-eclampsia (PE) or fetal growth restriction (FGR). Pregnant women were classified as follows: (group 1) pregnancies without PE or FGR (n=16), (group 2) pregnancies with PE or FGR but without MgSO4 administration (n=14), and (group 3) pregnancies with PE or FGR and with MgSO4 administration (n=28). We observed the localization of PMCA and SERCA-2 in placentas and compared its expression among 3 groups. And we observed its expression in BeWo cells following treatment with MgSO4 and CoCl2 PMCA staining was more observed in the basal membrane, whereas SERCA-2 staining was observed predominantly under the microvillous membrane. SERCA-2 expression was significantly increased in group 3 compared with that in group 1. Considering the gestational age at delivery, PMCA expression was increased in group 2 and group 3 compared with that in group 1 after 36 weeks of gestation. SERCA-2 was increased in group 3, but not in group 2 compared with that in group 1 after 36 weeks of gestation. In BeWo cells, MgSO4 treatment increased PMCA and SERCA-2 expression. PMCA expression was influenced by gestational age at delivery, and SERCA-2 expression was increased in the presence of PE and antepartal MgSO4 administration. This indicates that antepartal MgSO4 administration has a greater influence on SERCA-2 than PMCA. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10815589
Volume :
67
Issue :
2
Database :
Complementary Index
Journal :
Journal of Investigative Medicine (Sage Publications Inc.)
Publication Type :
Academic Journal
Accession number :
134365413
Full Text :
https://doi.org/10.1136/jim-2018-000844