Sex difference in GPER expression does not change vascular relaxation or reactive oxygen species generation in rat mesenteric resistance arteries

被引:14
作者
Peixoto, Pollyana [1 ]
da Silva, Josiane Fernandes [2 ]
Aires, Rosaria Dias [2 ]
Costa, Eduardo Damasceno [2 ]
Lemos, Virginia Soares [2 ]
Bissoli, Nazare Souza [1 ]
dos Santos, Roger Lyrio [1 ]
机构
[1] Univ Fed Espirito Santo, Dept Physiol Sci, Ave Marechal Campos 1468, BR-29050755 Vitoria, ES, Brazil
[2] Univ Fed Minas Gerais, Dept Physiol & Biophys, Belo Horizonte, MG, Brazil
关键词
GPER; Sex difference; Oxidative stress; Vascular relaxation; Mesenteric resistance arteries; 17; BETA-ESTRADIOL; ESTROGEN-RECEPTOR; NITRIC-OXIDE; ENDOTHELIAL DYSFUNCTION; OXIDATIVE STRESS; AGONIST G-1; CORONARY VASODILATION; SUPEROXIDE-DISMUTASE; GENDER-DIFFERENCES; NAD(P)H OXIDASE;
D O I
10.1016/j.lfs.2018.09.036
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Aim: An imbalance between antioxidant and pro-oxidant factors, with a predominance of the latter, characterises oxidative stress and is indicative of a loss of vascular function. The beneficial vascular effects of oestrogen may be related to its ability to stimulate the G protein-coupled oestrogen receptor (GPER) and produce antioxidant activity. This study evaluated the GPER-dependent relaxation response in the mesenteric resistance arteries of female and male rats and measured the contributions of pro-oxidant and antioxidant enzymes in this response. Main methods: The relaxation response was characterised in third-order mesenteric arteries using concentration-response curves of the selective GPER agonist G-1 (1 nM-10 mu M), target protein levels were measured using Western blots, and vascular superoxide anion (O-2 center dot(-)) and hydrogen peroxide (H2O2) levels were measured using dihydroethidium (DHE) and dichlorofluorescein (DCF) staining, respectively. Key findings: The GPER agonist induced concentration-dependent vasorelaxation without showing differences between sexes. However, GPER expression was greater in male rats. No sex differences were detected in the expression of antioxidant proteins (catalase, SOD-1, and SOD-2). The basal vascular production of O-2 center dot(-) and H2O2 was similar in the studied groups, and stimulation with G-1 maintained this response. Significance: Together, our results show that the expression of GPER is greater in male mesenteric arteries, despite of the lack of a difference in vascular response. Nevertheless, antioxidant enzyme expression levels and the generation rates of pro-oxidants were similar between the studied groups. These results offer a new perspective for understanding GPER expression and functionality in resistance arteries.
引用
收藏
页码:198 / 205
页数:8
相关论文
共 79 条
[51]  
MARCONDES F. K., 2002, Braz. J. Biol., V62, P609, DOI 10.1590/S1519-69842002000400008
[52]   Expression and intracellular distribution of the G protein-coupled receptor 30 in rat hippocampal formation [J].
Matsuda, KenIchi ;
Sakamoto, Hirotaka ;
Mori, Hiroko ;
Hosokawa, Koji ;
Kawamura, Akeo ;
Itose, Minoru ;
Nishi, Mayumi ;
Prossnitz, Eric R. ;
Kawata, Mitsuhiro .
NEUROSCIENCE LETTERS, 2008, 441 (01) :94-99
[53]   HUMAN-DISEASE, FREE-RADICALS, AND THE OXIDANT/ANTIOXIDANT BALANCE [J].
MCCORD, JM .
CLINICAL BIOCHEMISTRY, 1993, 26 (05) :351-357
[54]   Obligatory role for GPER in cardiovascular aging and disease [J].
Meyer, Matthias R. ;
Fredette, Natalie C. ;
Daniel, Christoph ;
Sharma, Geetanjali ;
Amann, Kerstin ;
Arterburn, Jeffrey B. ;
Barton, Matthias ;
Prossnitz, Eric R. .
SCIENCE SIGNALING, 2016, 9 (452)
[55]   Effect of gender and sex hormones on vascular oxidative stress [J].
Miller, Alyson A. ;
De Silva, T. Michael ;
Jackman, Katherine A. ;
Sobey, Christopher G. .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2007, 34 (10) :1037-1043
[56]   Effect of gender on NADPH-oxidase activity, expression, and function in the cerebral circulation - Role of estrogen [J].
Miller, Alyson A. ;
Drummond, Grant R. ;
Mast, Anja E. ;
Schmidt, Harald H. H. W. ;
Sobey, Christopher G. .
STROKE, 2007, 38 (07) :2142-2149
[57]   Role for hydrogen peroxide in flow-induced dilation of human coronary arterioles [J].
Miura, H ;
Bosnjak, JJ ;
Ning, G ;
Saito, T ;
Miura, M ;
Gutterman, DD .
CIRCULATION RESEARCH, 2003, 92 (02) :E31-E40
[58]  
Muller G, 2009, ANTIOXID REDOX SIGN, V11, P1711, DOI 10.1089/ARS.2008.2403
[59]   Role for NADPH/NADH oxidase in the modulation of vascular tone [J].
Münzel, T ;
Hink, U ;
Heitzer, T ;
Meinertz, T .
HEART IN STRESS, 1999, 874 :386-400
[60]   G Protein-Coupled Estrogen Receptor Agonist Improves Cerebral Microvascular Function After Hypoxia/Reoxygenation Injury in Male and Female Rats [J].
Murata, Takahiro ;
Dietrich, Hans H. ;
Xiang, Chuanxi ;
Dacey, Ralph G., Jr. .
STROKE, 2013, 44 (03) :779-+