Back to Search Start Over

Expression of adipokines and their receptors in adipose tissue of women with class 3 obesity with or without hypertension.

Authors :
Cano-Martínez LJ
Marroquín C
Coral-Vázquez RM
Méndez JP
Trejo S
Campos Pérez FJ
Pérez-Razo JC
Canto P
Source :
Gene [Gene] 2019 Jun 20; Vol. 702, pp. 148-152. Date of Electronic Publication: 2019 Mar 30.
Publication Year :
2019

Abstract

Obesity increases the risk of developing hypertension. Since both pathological entities constitute public health problems, the aim of this study was to investigate RNA expression of adiponectin, leptin and their receptors in adipose tissue in women with class 3 obesity, with or without hypertension. Serum concentrations of these adipokines were also quantitated. Women with obesity and hypertension (n = 22) and with obesity without hypertension (n = 37) were included. All patients presented class 3 obesity, without diabetes mellitus. The expression of mRNA in: adiponectin, ADIPOR1 and ADIPOR2 was analyzed in visceral (VAT) and subcutaneous (SAT) adipose tissue; leptin and its receptor were only analyzed in SAT, by reverse transcription quantitative PCR. Measurements of adiponectin and leptin concentrations were performed using enzyme-linked immunosorbent assay kits. Analysis of mRNA expressions in VAT and SAT are presented as median and quartiles. Analysis of serum concentrations of adipokines are presented as median and percentiles 25th-75th. Women presenting a higher mean arterial pressure, had significantly higher levels of mRNA expression of adiponectin in SAT. Besides, we found several significant positive correlations of these adipokines and their receptors. In conclusion, we found that those women with a higher mean arterial pressure and receiving antihypertensive treatment, presented higher levels of mRNA expression of adiponectin in SAT.<br /> (Copyright © 2019. Published by Elsevier B.V.)

Details

Language :
English
ISSN :
1879-0038
Volume :
702
Database :
MEDLINE
Journal :
Gene
Publication Type :
Academic Journal
Accession number :
30940525
Full Text :
https://doi.org/10.1016/j.gene.2019.03.070