Department of Pharmacology, Ribeirao Preto Medical School, University of São Paulo São Paulo Brazil.
Department of Pharmacology, Biological Sciences Institute, Federal University of Minas Gerais Belo Horizonte, Brazil.
Front Pharmacol. 2015 Mar 2;6:34. doi: 10.3389/fphar.2015.00034. eCollection 2015.
Aldosterone promotes non-genomic effects in endothelial and vascular smooth muscle cells via activation of mineralocorticoid receptors (MR) and G protein-coupled estrogen receptors (GPER). GPER activation is associated with beneficial/protective effects in the vasculature. Considering that vascular dysfunction plays a major role in diabetes-associated complications, we hypothesized that the beneficial effects mediated by vascular GPER activation, in response to aldosterone, are decreased in diabetes. Mesenteric resistance arteries from female, 14-16 weeks-old, control and diabetic (db/db) mice were used. Phenylephrine (PhE)-induced contractions were greater in arteries from db/db vs. control mice. Aldosterone (10 nM) increased maximal contractile responses to PhE in arteries from control mice, an effect elicited via activation of GPER. Although aldosterone did not increase PhE responses in arteries from db/db mice, blockade of GPER, and MR decreased PhE-induced contractile responses in db/db mesenteric arteries. Aldosterone also reduced the potency of acetylcholine (ACh)-induced relaxation in arteries from both control and db/db mice via MR-dependent mechanisms. GPER antagonism further decreased ACh-induced relaxation in the control group, but did not affect ACh responses in the diabetic group. Aldosterone increased extracellular signal-regulated kinase 1/2 phosphorylation in arteries from control and db/db mice by a GPER-dependent mechanism. GPER, but not MR, gene, and protein expression, determined by RT-PCR and immunoblotting/immunofluorescence assays, respectively, were increased in arteries from db/db mice vs. control arteries. These findings indicate that aldosterone activates both vascular MR and GPER and that the beneficial effects of GPER activation are decreased in arteries from diabetic animals. Our results further elucidate the mechanisms by which aldosterone influences vascular function and contributes to vascular dysfunction in diabetes. Financial Support: FAPESP, CNPq, and CAPES, Brazil.
醛固酮通过激活盐皮质激素受体 (MR) 和 G 蛋白偶联雌激素受体 (GPER) 促进内皮细胞和血管平滑肌细胞的非基因组效应。GPER 的激活与血管中的有益/保护作用有关。考虑到血管功能障碍在糖尿病相关并发症中起主要作用,我们假设醛固酮介导的血管 GPER 激活的有益作用在糖尿病中减少。使用来自雌性、14-16 周龄的对照和糖尿病 (db/db) 小鼠的肠系膜阻力动脉。与对照小鼠相比,db/db 小鼠的血管对苯肾上腺素 (PhE) 诱导的收缩更大。醛固酮 (10 nM) 增加了对照小鼠血管对 PhE 的最大收缩反应,这是通过激活 GPER 引起的。尽管醛固酮没有增加 db/db 小鼠血管对 PhE 的反应,但 GPER 和 MR 的阻断降低了 db/db 肠系膜动脉对 PhE 诱导的收缩反应。醛固酮还通过 MR 依赖性机制降低了来自对照和 db/db 小鼠的乙酰胆碱 (ACh) 诱导的舒张的效力。GPER 拮抗剂进一步降低了对照组的 ACh 诱导的舒张,但对糖尿病组的 ACh 反应没有影响。醛固酮通过 GPER 依赖性机制增加了来自对照和 db/db 小鼠的血管细胞外信号调节激酶 1/2 磷酸化。通过 RT-PCR 和免疫印迹/免疫荧光测定分别确定的 GPER,但不是 MR,基因和蛋白表达,在 db/db 小鼠的血管中增加,而在对照血管中则降低。这些发现表明,醛固酮激活血管 MR 和 GPER,并且 GPER 激活的有益作用在糖尿病动物的血管中减少。我们的研究结果进一步阐明了醛固酮影响血管功能的机制,并导致糖尿病中的血管功能障碍。资金支持:FAPESP、CNPq 和 CAPES,巴西。