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Am J Physiol Lung Cell Mol Physiol 261: L23-L26, 1991;
1040-0605/91 $5.00
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Ca2+-ATPase and function of sarcoplasmic reticulum during cardiac hypertrophy

Dmitri Levitsky 1, Diane De La Bastie 1, Ketty Schwartz 1, and Anne-Marie Lompré 1

1 INSERM U 127, Hopital Lariboisière, 75010 Paris, France; and Laboratory of Membranes and Ion Transport, Institute of Experimental Cardiology, USSR Cardiology Research Center, Moscow 121552, USSR

The properties of the calcium pump system of sarcoplasmic reticulum (SR) were studied in a series of 34 rats subjected to cardiac overload and 19 sham-operated animals. Total homogenates of left ventricle were analyzed by measuring the oxalate-supported Ca2+ uptake rate, the steady-state level of the phosphorylated intermediate of Ca2+-adenosine triphosphatase (Ca2+-ATPase) (E-P), and the amount of Ca2+-ATPase mRNA. All three parameters decreased gradually as a function of the relative left ventricular weight increase. The calcium-sensitivity curves showed that the velocity of Ca2+ transport in SR from the hypertrophied heart is diminished at low as well as optimal Ca2+ concentrations, with the dissociation constant (Kd) value for Ca2+ unchanged from that of the control preparation. Taken together with the results presented in our recent publication (De la Bastie, Levitsky, Mercadier, Marotte, Wisnewsky, Brovkovivh, Schwartz, and Lompré, Circ. Res. 66: 554–564, 1990), these data strongly indicate that differences in the Ca2+ pump activities of SR from normal and hypertrophied rat hearts are due to quantitative rather than qualitative changes of the Ca2+-ATPase protein.

calcium ion uptake; calcium ion adenosine triphosphatase messenger ribonucleic acid; cardiac hypertrophy; monoclonal antibody




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