Changes in the expression of cardiac Na+-K+ ATPase subunits in the UM-X7.1 cardiomyopathic hamster

被引:17
作者
Kato, K
Lukas, A
Chapman, DC
Dhalla, NS
机构
[1] St Boniface Gen Hosp, Res Ctr, Inst Cardiovasc Sci, Winnipeg, MB R2H 2A6, Canada
[2] Univ Manitoba, Fac Med, Dept Physiol, Winnipeg, MB R2H 2A6, Canada
基金
英国医学研究理事会;
关键词
sarcolemmal Na+-K+ ATPase; genetic cardiomyopathy; UM-X7.1; hamster; cardiac Na+-K+ ATPase subunits;
D O I
10.1016/S0024-3205(00)00709-8
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Previous studies have shown that cardiac Na+-K+ ATPase activity in the UM-X7.1 hamster strain is decreased at an early stage of genetic cardiomyopathy and remains depressed; however, the mechanism for this decrease is unknown. The objective of the present study was to assess whether changes in the expression of cardiac Na+ -K+ ATPase subunits in control and UM-X7.1 cardiomyopathic hamsters are associated with alterations in the enzyme activity. Accordingly, we examined sarcolemmal Na+-K+ ATPase activity as well as protein content and mRNA levels for the alpha(1), alpha(2), alpha(3), and beta(1)-subunit of the Na+-K+ ATPase in 250-day-old UM-X7.1 and age-matched, control Syrian hamsters; this age corresponds to the severe stage of heart failure in the UM-X7.1 hamster. Na+-K+ ATPase activity in UM-X7.1 hearts was decreased compared to controls (9.0 +/- 0.8 versus 5.6 +/- 0.8 mu mol Pi/mg protein/hr), Western blot analysis revealed that the protein content of Na+-K+ ATPase alpha(1)- and beta(1)-subunits were increased to 164 +/- 27% and 146 +/- 22% in UM-X7.1 hearts respectively, whereas that of the or,and alpha(3)-subunits were decreased to 82 +/- 5% and 69 +/- 11% of control values. The results of Northern blot analysis for mRNA levels were consistent with the protein levels; mRNA levels for the alpha(1)- and beta(1)-subunits in UM-X7.1 hearts were elevated to 165 +/- 14% and 151 +/- 10%, but the alpha(2)-subunit was decreased to 60 +/- 8% of the control value. We were unable to detect mRNA for the alpha(3)-subunit in either UM-X7.1 or control hearts. These data suggest that the marked depression of Na+-K+ ATPase activity in UM-X7.1 cardiomyopathic hearts may be due to changes in the expression of subunits for this enzyme. (C) 2000 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:1175 / 1183
页数:9
相关论文
共 35 条
  • [11] HIATT A, 1984, J BIOL CHEM, V259, P2629
  • [12] RED CELL MEMBRANE AND TRANSPORT OF SODIUM AND POTASSIUM
    HOFFMAN, JF
    [J]. AMERICAN JOURNAL OF MEDICINE, 1966, 41 (05) : 666 - &
  • [13] HEREDITARY POLYMYOPATHY AND CARDIOMYOPATHY IN THE SYRIAN-HAMSTER .1. PROGRESSION OF HEART AND SKELETAL-MUSCLE LESIONS IN THE UM-X7.1 LINE
    JASMIN, G
    PROSCHEK, L
    [J]. MUSCLE & NERVE, 1982, 5 (01) : 20 - 25
  • [14] Jasmin G, 1979, Ann N Y Acad Sci, V317, P46, DOI 10.1111/j.1749-6632.1979.tb37324.x
  • [15] JEWELL EA, 1991, J BIOL CHEM, V266, P16925
  • [16] KANEKO M, 1989, AM J PHYSIOL, V257, pH803
  • [17] Alterations of heart function and Na+-K+-ATPase activity by etomoxir in diabetic rats
    Kato, K
    Chapman, DC
    Rupp, H
    Lukas, A
    Dhalla, NS
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 1999, 86 (03) : 812 - 818
  • [18] Mechanism of depression in cardiac sarcolemmal Na+-K+-ATPase by hypochlorous acid
    Kato, K
    Shao, QM
    Elimban, V
    Lukas, A
    Dhalla, NS
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1998, 275 (03): : C826 - C831
  • [19] Larsen JS, 1997, MOL CELL BIOCHEM, V169, P85
  • [20] SIGNIFICANCE OF SODIUM-PUMP ISOFORMS IN DIGITALIS THERAPY
    MCDONOUGH, AA
    WANG, JN
    FARLEY, RA
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1995, 27 (04) : 1001 - 1009