» Articles » PMID: 35213910

Expression of Endothelin-1 and Endothelial Nitric Oxide Synthase in Normal and Preeclamptic Placentae

Overview
Date 2022 Feb 25
PMID 35213910
Authors
Affiliations
Soon will be listed here.
Abstract

Objective:  To investigate the expression of endothelin-1 (ET-1) and endothelial nitric oxide (NO) synthase (eNOS) in normal and preeclamptic (PE) placentae.

Methods:  The present cross-sectional analytical study was performed in normal and PE primigravidae ( = 10 in each group) who were admitted to the North Okkalapa General and Teaching Hospital from February 2019 to February 2020. Serum samples were collected immediately before delivery, and placental tissues were collected immediately after emergency or elective cesarean section. The expression of placental eNOS was measured by western blot, and the levels of ET-1 in placental tissue homogenates and in the serum were measured by enzyme-linked immunosorbent assay (ELISA).

Results:  The PE group had significantly higher serum levels of ET-1 (median: 116.56 pg/mL; IQR: 89.14-159.62 pg/mL) than the normal group (median: 60.02 pg/mL; IQR: 50.89-94.37 pg/mL) ( < 0.05). However, statistically significant differences were not observed in the levels of ET-1 in placental tissue homogenates between normal and PE placentae (median: 0.007 pg/µg of total protein; IQR: 0.002-0.0123 pg/µg of total protein; and median: 0.005 pg/µg of total protein; IQR: 0.003-0.016 pg/µg of total protein respectively). The median and IQR values of relative placental eNOS expression were significantly higher in the PE group than in the normal group ( < 0.05). The serum levels of ET-1 level were not significantly correlated with placental ET-1 expression, and neither there was a significant correlation between placental ET-1 and eNOS expression in any of the groups.

Conclusion:  The serum levels of ET-1 were significantly higher in PE pregnant women compared with normal pregnant women, while the ET-1 levels of placental tissue homogenates were not significantly different. Serum ET-1 rather than placental ET-1 might play a major role in the pathogenesis of PE.

Citing Articles

Plasma eNOS Concentration in Healthy Pregnancy and in Hypertensive Disorders of Pregnancy: Evidence of Reduced Concentrations in Pre-Eclampsia from Two Independent Studies.

Kaihara J, Minami C, Peracoli M, Romao-Veiga M, Ribeiro-Vasques V, Peracoli J Diseases. 2023; 11(4).

PMID: 37987266 PMC: 10660730. DOI: 10.3390/diseases11040155.


Gestational intermittent hypoxia induces endothelial dysfunction and hypertension in pregnant rats: role of endothelin type B receptor†.

Song R, Yadav P, Dangudubiyyam S, Hofmann A, Mishra J, Kumar S Biol Reprod. 2023; 110(1):185-197.

PMID: 37823770 PMC: 11484499. DOI: 10.1093/biolre/ioad139.

References
1.
Ghabour M, Eis A, Brockman D, Pollock J, Myatt L . Immunohistochemical characterization of placental nitric oxide synthase expression in preeclampsia. Am J Obstet Gynecol. 1995; 173(3 Pt 1):687-94. DOI: 10.1016/0002-9378(95)90324-0. View

2.
Napolitano M, Miceli F, Calce A, Vacca A, Gulino A, Apa R . Expression and relationship between endothelin-1 messenger ribonucleic acid (mRNA) and inducible/endothelial nitric oxide synthase mRNA isoforms from normal and preeclamptic placentas. J Clin Endocrinol Metab. 2000; 85(6):2318-23. DOI: 10.1210/jcem.85.6.6623. View

3.
Myatt L, Eis A, Brockman D, Greer I, Lyall F . Endothelial nitric oxide synthase in placental villous tissue from normal, pre-eclamptic and intrauterine growth restricted pregnancies. Hum Reprod. 1997; 12(1):167-72. DOI: 10.1093/humrep/12.1.167. View

4.
Wang Y, Gu Y, Zhang Y, Lewis D . Evidence of endothelial dysfunction in preeclampsia: decreased endothelial nitric oxide synthase expression is associated with increased cell permeability in endothelial cells from preeclampsia. Am J Obstet Gynecol. 2004; 190(3):817-24. DOI: 10.1016/j.ajog.2003.09.049. View

5.
Brosens I . A STUDY OF THE SPIRAL ARTERIES OF THE DECIDUA BASALIS IN NORMOTENSIVE AND HYPERTENSIVE PREGNANCIES. J Obstet Gynaecol Br Commonw. 1964; 71:222-30. DOI: 10.1111/j.1471-0528.1964.tb04270.x. View