Mineralocorticoid Receptor-Dependent Proximal Tubule Injury Is Mediated by a Redox-Sensitive mTOR/S6K1 Pathway

被引:32
|
作者
Whaley-Connell, Adam T. [1 ,2 ,3 ,4 ,7 ]
Habibi, Javad [1 ,2 ,3 ,4 ,8 ]
Nistala, Ravi [1 ,2 ,3 ,4 ,7 ]
DeMarco, Vincent G. [1 ,2 ,3 ,4 ,5 ,8 ]
Pulakat, Lakshmi [1 ,2 ,3 ,4 ,6 ,7 ,8 ]
Hayden, Melvin R. [2 ,3 ,4 ,8 ]
Joginpally, Tejaswini [1 ,3 ]
Ferrario, Carlos M. [9 ]
Parrish, Alan R. [2 ,5 ,7 ]
Sowers, James R. [1 ,2 ,3 ,4 ,5 ,8 ]
机构
[1] Harry S Truman VA Med Ctr, Columbia, MO 65211 USA
[2] Univ Missouri, Sch Med, Columbia, MO USA
[3] Diabet & Cardiovasc Ctr, Columbia, MO USA
[4] Dept Internal Med, Columbia, MO USA
[5] Dept Med Pharmacol & Physiol, Columbia, MO USA
[6] Dept Nutr & Exercise Physiol, Columbia, MO USA
[7] Div Nephrol & Hypertens, Columbia, MO USA
[8] Div Endocrinol & Metab, Columbia, MO USA
[9] Wake Forest Univ, Winston Salem, NC 27109 USA
关键词
Cadherin; Megalin; beta-NAG; Proteinuria; EPITHELIAL-MESENCHYMAL TRANSITION; SMOOTH-MUSCLE-CELLS; ANGIOTENSIN-II; OXIDATIVE STRESS; NADPH OXIDASE; MTOR PATHWAY; N-CADHERIN; KINASE; ALDOSTERONE; ACTIVATION;
D O I
10.1159/000335079
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background/Aims: The mammalian target of rapamycin (mTOR) is a serine kinase that regulates phosphorylation (p) of its target ribosomal 56 kinase (S6K1), whose activation can lead to glomerular and proximal tubular cell (PTC) injury and associated proteinuria. Increased mTOR/S6K1 signaling regulates signaling pathways that target fibrosis through adherens junctions. Recent data indicate aldosterone signaling through the mineralocorticoid receptor (MR) can activate the mTOR pathway. Further, antagonism of the MR has beneficial effects on proteinuria that occur independent of hemodynamics. Methods: Accordingly, hypertensive transgenic TG(mRen2)27 (Ren2) rats, with elevated serum aldosterone and proteinuria, and age-matched Sprague-Dawley rats were treated with either a low dose (1 mg/kg/day) or a conventional dose (30 mg/kg/day) of spironolactone (MR antagonist) or placebo for 3 weeks. Results: Ren2 rats displayed increases in urine levels of the PTC brush border lysosomal enzyme N-acetyl-beta-aminoglycosidase beta-NAG) in conjunction with reductions in PTC megalin, the apical membrane adherens protein T-cadherin and basolateral alpha-(E)-catenin, and fibrosis. In concert with these abnormalities, Ren2 renal cortical tissue also displayed increased Ser2448 (p)/activation of mTOR and Thr389 (p)-S6K1 and increased 3-nitrotyrosine (3-NT) content, a marker for peroxynitrite. Low-dose spironolactone had no effect on blood pressure but decreased proteinuria and beta-NAG comparable to a conventional dose of this MR antagonist. Both doses of spironolactone attenuated ultrastructural maladaptive alterations and led to comparable reductions in (p)-mTOR/(p)-S6K1, 3-NT, fibrosis, and increased expression of alpha-(E)-catenin, T-and N-cadherin. Conclusions: Thereby, MR antagonism improves proximal tubule integrity by targeting mTOR/S6K1 signaling and redox status independent of changes in blood pressure. Copyright (C) 2011 S. Karger AG, Basel
引用
收藏
页码:90 / 100
页数:11
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