Aldosteronism: an immunostimulatory state precedes proinflammatory/fibrogenic cardiac phenotype

被引:97
作者
Gerling, IC
Sun, Y
Ahokas, RA
Wodi, LA
Bhattacharya, SK
Warrington, KJ
Postlethwaite, AE
Weber, KT
机构
[1] Univ Tennessee, Ctr Hlth Sci, Dept Med, Div Cardiovasc Dis, Memphis, TN 38163 USA
[2] Univ Tennessee, Ctr Hlth Sci, Dept Med, Div Endocrinol, Memphis, TN 38163 USA
[3] Univ Tennessee, Ctr Hlth Sci, Dept Med, Div Connect Tissue Dis, Memphis, TN 38163 USA
[4] Univ Tennessee, Ctr Hlth Sci, Dept Obstet & Gynecol, Memphis, TN 38163 USA
[5] Univ Tennessee, Ctr Hlth Sci, Dept Surg, Memphis, TN 38163 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2003年 / 285卷 / 02期
关键词
peripheral blood mononuclear cells; ionized magnesium; oxidative and nitrosative stress; transcriptome; pathology;
D O I
10.1152/ajpheart.00113.2003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chronic inappropriate ( relative to dietary Na+ intake) elevations in circulating aldosterone ( ALDO), termed aldosteronism, are associated with remodeling of intramural arteries of the right and left heart. Lesions appear at week 4 of treatment with ALDO and 1% dietary NaCl in uninephrectomized rats (ALDOST) and include invading monocytes, macrophages and lymphocytes with intracellular evidence of oxidative and nitrosative stress, myofibroblasts, and perivascular fibrosis. In this study, we tested the hypothesis that an immunostimulatory state with activated circulating peripheral blood mononuclear cells (PB-MCs) precedes this proinflammatory and profibrogenic cardiac phenotype and is initiated by reduction in the cytosolic free Mg2+ concentration ([Mg2+](i)). At 1 and 4 wk of ALDOST ( preclinical and clinical stages, respectively), we monitored serum Mg2+, PBMC [Mg2+](i) and cytosolic free [Ca2+] (via fluorimetry), and expressed genes ( via microchip array) as well as markers of oxidative and nitrosative stress in plasma [alpha(1)-antiproteinase activity (alpha(1)-AP)] and cardiac tissue ( immunohistochemical detection of gp91(phox) subunit of NADPH oxidase and 3-nitrotyrosine). Age- and gender-matched unoperated and untreated (UO) rats and uninephrectomized salt-treated (UN) rats served as controls. Serum [Mg2+] was unchanged by ALDOST. In contrast with UO and UN, [Mg2+](i) and plasma alpha(1)-AP were each reduced (P < 0.05) at weeks 1 and 4. The decline in PBMC [Mg2+](i) was accompanied by Ca2+ loading. Differential ( twofold and higher) expression (up- and downregulation) in PBMC transcriptomes was present at week 1 and progressed at week 4. Involved were genes for the α(1)-isoform of Na+-K+-ATPase, the ATP-dependent Ca2+ pump, antioxidant reserves, inducible nitric oxide synthase, and PBMC activation with autoimmune responses. Expression of 3-nitrotyrosine and activation of gp91(phox) were seen in inflammatory cells that invaded intramural arteries. Thus early in aldosteronism ( preclinical stage), an immunostimulatory state featuring activated circulating PBMCs with reduced ionized [Mg2+](i) and oxidative and nitrosative stress precedes and may even predispose to coronary vascular lesions that first appear at week 4. peripheral blood mononuclear cells; ionized magnesium; oxidative and nitrosative stress; transcriptome; pathology
引用
收藏
页码:H813 / H821
页数:9
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