Diminished expression of sarcoplasmic reticulum Ca2+-ATPase and ryanodine sensitive Ca2+ channel mRNA in streptozotocin-induced diabetic rat heart

被引:92
作者
Teshima, Y [1 ]
Takahashi, N [1 ]
Saikawa, T [1 ]
Hara, M [1 ]
Yasunaga, S [1 ]
Hidaka, S [1 ]
Sakata, T [1 ]
机构
[1] Oita Med Univ, Sch Med, Dept Internal Med 1, Oita 8795593, Japan
关键词
streptozotocin-induced diabetes mellitus; down-regulation of mRNA; western blot analysis; insulin supplementation; sarcoplasmic reticulum calcium-adenosine triphosphatase; L-type Ca2+ channel; ryanodine sensitive Ca2+ channel; Na+-Ca2+ exchanger;
D O I
10.1006/jmcc.2000.1107
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The diabetic heart has an abnormal intracellular calcium ([Ca2+]i) metabolism. However, the responsible molecular mechanisms are unclear. The present study aimed to investigate mRNAs expressed in the proteins which regulate heart [Ca2+]i metabolism in streptozotocin (STZ)-induced diabetic rats. Expression of sarcoplasmic reticulum Ca2+-adenosine triphosphatase (SR Ca2+-ATPase) mRNA was significantly less in the heart 3 weeks after STZ injection than that in the age-matched controls. Together with the down-regulation of SR Ca2+-ATPase, expression of ryanodine sensitive Ca2+ channel (RYR) mRNA was also decreased 12 weeks after STZ injection. Insulin supplementation fully restored the decreased mRNAs expression of SR Ca2+-ATPase and RYR. The diminished expression and restoration with insulin supplementation of SR Ca2+-ATPase was further confirmed at the protein level. In contrast, expression of mRNAs coding the L-type Ca2+ channel, Na+-Ca2+ exchanger, or phospholamban were not affected 3 or 12 weeks after STZ injection. These results can be taken to indicate that the down-regulation of SR Ca2+-ATPase and RYR mRNAs is a possible underlying cause of cardiac dysfunction in STZ-induced diabetic rats. (C) 2000 Academic Press.
引用
收藏
页码:655 / 664
页数:10
相关论文
共 21 条
[1]   INFLUENCE OF EXPERIMENTAL DIABETES ON SARCOPLASMIC-RETICULUM FUNCTION IN RAT VENTRICULAR MUSCLE [J].
BOUCHARD, RA ;
BOSE, D .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 260 (02) :H341-H354
[2]   ALTERED MYOCARDIAL MECHANICS IN DIABETIC RATS [J].
FEIN, FS ;
KORNSTEIN, LB ;
STROBECK, JE ;
CAPASSO, JM ;
SONNENBLICK, EH .
CIRCULATION RESEARCH, 1980, 47 (06) :922-933
[3]   DIABETIC CARDIOMYOPATHY [J].
FEIN, FS ;
SONNENBLICK, EH .
CARDIOVASCULAR DRUGS AND THERAPY, 1994, 8 (01) :65-73
[4]   DEFECTIVE SARCOPLASMIC RETICULAR CALCIUM-TRANSPORT IN DIABETIC CARDIOMYOPATHY [J].
GANGULY, PK ;
PIERCE, GN ;
DHALLA, KS ;
DHALLA, NS .
AMERICAN JOURNAL OF PHYSIOLOGY, 1983, 244 (06) :E528-E535
[5]   DIABETIC CARDIOMYOPATHY [J].
HAMBY, RI ;
ZONERAICH, S ;
SHERMAN, L .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1974, 229 (13) :1749-1754
[6]   ROLE OF DIABETES IN CONGESTIVE HEART-FAILURE - FRAMINGHAM STUDY [J].
KANNEL, WB ;
HJORTLAND, M ;
CASTELLI, WP .
AMERICAN JOURNAL OF CARDIOLOGY, 1974, 34 (01) :29-34
[7]   Altered Ca2+ handling in ventricular myocytes isolated from diabetic rats [J].
LagadicGossmann, D ;
Buckler, KJ ;
LePrigent, K ;
Feuvray, D .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1996, 270 (05) :H1529-H1537
[8]   CARDIAC SARCOPLASMIC-RETICULUM FUNCTION IN INSULIN-TREATED OR CARNITINE-TREATED DIABETIC RATS [J].
LOPASCHUK, GD ;
TAHILIANI, AG ;
VADLAMUDI, RVSV ;
KATZ, S ;
MCNEILL, JH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1983, 245 (06) :H969-H976
[9]   CLONING OF THE RAT-HEART NA+-CA-2+ EXCHANGER AND ITS FUNCTIONAL EXPRESSION IN HELA-CELLS [J].
LOW, W ;
KASIR, J ;
RAHAMIMOFF, H .
FEBS LETTERS, 1993, 316 (01) :63-67
[10]   Expression of cardiac calcium regulatory proteins in atrium v ventricle in different species [J].
Lüss, I ;
Boknik, P ;
Jones, LR ;
Kirchhefer, U ;
Knapp, J ;
Linck, B ;
Lüss, H ;
Meissner, A ;
Müller, FU ;
Schmitz, W ;
Vahlensieck, U ;
Neumann, J .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1999, 31 (06) :1299-1314