Overexpression of sarcoplasmic reticulum Ca2+-ATPase improves cardiac contractile function in hypothyroid mice

被引:28
作者
Bluhm, WF [1 ]
Meyer, M [1 ]
Sayen, MR [1 ]
Swanson, EA [1 ]
Dillmann, WH [1 ]
机构
[1] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
关键词
contractile function; gene expression; SR; cardiomyopathy; E-C coupling;
D O I
10.1016/S0008-6363(99)00109-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Prolonged cardiac contraction and relaxation in hypothyroidism are in part related to diminished expression of the gene coding for the calcium pump of the sarcoplasmic reticulum (SERCA2a). Therefore, we examined whether or not transgenic SERCA2a gene expression in mice may compensate for the cardiac effects of hypothyroidism. Methods: SERCA2a mRNA and protein were analyzed from hearts of euthyroid and hypothyroid mice of wild-type or SERCA2a transgene status. Contractile function was studied in isolated left ventricular papillary muscles. Results: We found significant decreases of SERCA2a mRNA and protein levels in hearts of hypothyroid wild-type mice in comparison with euthyroid wild-type mice (controls). Papillary muscles from hypothyroid wild-type mice showed significant increases in time to peak contraction and relaxation times compared with controls. In contrast, SERCA2a mRNA and protein levels were significantly higher in hypothyroid SERCA2a transgenic mice than in hypothyroid wild-type mice. The transgene led to a functional improvement by compensating for the prolonged contraction and relaxation of papillary muscles. Conclusions: Our murine model of hypothyroidism revealed decreases in SERCA2a gene expression accompanied by prolonged contraction and relaxation of papillary muscles, and an improvement of the contractile phenotype due to compensated SERCA2a gene expression in SERCA2a transgenic mice. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:382 / 388
页数:7
相关论文
共 26 条
[1]   EFFECT OF THYROID-HORMONE ON THE EXPRESSION OF MESSENGER-RNA ENCODING SARCOPLASMIC-RETICULUM PROTEINS [J].
ARAI, M ;
OTSU, K ;
MACLENNAN, DH ;
ALPERT, NR ;
PERIASAMY, M .
CIRCULATION RESEARCH, 1991, 69 (02) :266-276
[2]   Targeted overexpression of the sarcoplasmic reticulum Ca2+-ATPase increases cardiac contractility in transgenic mouse hearts [J].
Baker, DL ;
Hashimoto, K ;
Grupp, IL ;
Ji, Y ;
Reed, T ;
Loukianov, E ;
Grupp, G ;
Bhagwhat, A ;
Hoit, B ;
Walsh, R ;
Marban, E ;
Periasamy, M .
CIRCULATION RESEARCH, 1998, 83 (12) :1205-1214
[3]  
BAROVSKY K, 1981, J PHARMACOL EXP THER, V217, P314
[4]   ALTERATIONS IN COLLAGEN CROSS-LINKING IMPAIR MYOCARDIAL-CONTRACTILITY IN THE MOUSE HEART [J].
CAPASSO, JM ;
ROBINSON, TF ;
ANVERSA, P .
CIRCULATION RESEARCH, 1989, 65 (06) :1657-1664
[5]   Genes and physiology: Molecular physiology in genetically engineered animals [J].
Chien, KR .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (04) :901-909
[6]   CARDIAC-MUSCLE DISEASES IN GENETICALLY-ENGINEERED MICE - EVOLUTION OF MOLECULAR PHYSIOLOGY [J].
CHIEN, KR .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1995, 269 (03) :H755-H766
[7]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[8]   FUNCTION OF THE SARCOPLASMIC-RETICULUM AND EXPRESSION OF ITS CA-2+-ATPASE GENE IN PRESSURE OVERLOAD-INDUCED CARDIAC-HYPERTROPHY IN THE RAT [J].
DELABASTIE, D ;
LEVITSKY, D ;
RAPPAPORT, L ;
MERCADIER, JJ ;
MAROTTE, F ;
WISNEWSKY, C ;
BROVKOVICH, V ;
SCHWARTZ, K ;
LOMPRE, AM .
CIRCULATION RESEARCH, 1990, 66 (02) :554-564
[9]   Cardiovascular indexes in the mouse at rest and with exercise: New tools to study models of cardiac disease [J].
Desai, KH ;
Sato, R ;
Schauble, E ;
Barsh, GS ;
Kobilka, BK ;
Bernstein, D .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1997, 272 (02) :H1053-H1061
[10]  
DILLMANN WH, 1989, ANNU REV MED, V40, P373