Attenuation of adverse cardiac effects in prednisolone-treated δ-sarcoglycan-deficient mice by mineralocorticoid-receptor-antagonism

被引:8
作者
Bauer, Ralf [1 ,2 ]
Blain, Alison [1 ]
Greally, Elizabeth [1 ]
Lochmueller, Hanns [1 ]
Bushby, Kate [1 ]
MacGowan, Guy A. [1 ,3 ]
Straub, Volker [1 ]
机构
[1] Newcastle Univ, Inst Human Genet, Int Ctr Life, Newcastle Upon Tyne NE1 3BZ, Tyne & Wear, England
[2] Univ Heidelberg Hosp, Dept Cardiol Angiol & Pneumol, D-69120 Heidelberg, Germany
[3] Freeman Rd Hosp, Dept Cardiol, Newcastle Upon Tyne NE7 7DN, Tyne & Wear, England
关键词
Spironolactone; Glucocorticoids; delta-Sarcoglycan; Cardiomyopathy muscular dystrophy; VASCULAR SMOOTH; ALDOSTERONE; DYSTROPHIN; HEART; SPIRONOLACTONE; HYPERTROPHY; COLLAGEN; FAILURE; COMPLEX; CARDIOMYOPATHY;
D O I
10.1016/j.nmd.2009.10.003
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We have tested the hypothesis that the adverse effects of glucocorticoids in the delta-sarcoglycan-deficient (Sgcd-null) mouse are due to additional mineralocorticoid effects. We investigated the effects of spironolactone, an unselective mineralocorticoid-receptor antagonist, on in vivo cardiac haemodynamics, cardiomyocyte damage and Fibrosis in prednisolone treated Sgcd-null mice. Oral spironolactone given to 8-week-old Sgcd-null non-steroid treated mice had beneficial effects on systolic function by improving myocardial contractility when assessed by pressure-volume loops. Given in combination with prednisolone, spironolactone prevented steroid-induced deterioration of cardiac haemodynamics and acute sarcolemmal damage but not cardiac fibrosis. This study demonstrates the beneficial effects of oral spironolactone on cardiac haemodynamics in Sgcd-null mice and its ability to prevent some of the adverse effects of glucocorticoids. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:21 / 28
页数:8
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