Myosin Synthesis and Degradation during Development of Cardiac Hypertrophy in the Rabbit
- 1 June 1972
- journal article
- research article
- Published by Wolters Kluwer Health in Circulation Research
- Vol. 30 (6) , 690-702
- https://doi.org/10.1161/01.res.30.6.690
Abstract
Metabolism of left ventricular myosin was studied in rabbits (2.7-3.2 kg) following banding of the ascending aorta (65% occlusion). In 26 rabbits the incorporation of amino acid into myosin was determined 2, 3, 4, 9, and 15 days after either stenosis or sham operation by injecting 3H-lysine (0.5 mc/kg) 4 hours before the animals were killed. In 32 rabbits the same dose of 3H-lysine was injected 24 hours before surgery, and disappearance of isotope from myosin was measured by killing the rabbits after 3, 5, 7, 10, or 16 days. Specific radioactivity of free lysine, myosin, and total proteins was determined in left ventricular samples from each animal. The experimental results indicate that: (1) left ventricular peak systolic pressure increased from 97 to 163 mm Hg; (2) the ratio of left ventricular weight to body weight increased about 16% (3) disappearance of free 3H-lysine was similar in rabbits with aortic stenosis and those with sham operations; (4) after the second day myosin synthesis was greater in rabbits with aortic coarctations, reaching a maximum increase of 117% on the tenth day; (5) synthesis of left ventricular total proteins also reached a maximum of about 56% on the tenth day; (6) the decrease in specific radioactivity of myosin in rabbits with aortic coarctation was slower than it was in sham-operated animals. The experimental results were analyzed by a computerized simulation of myosin metabolism which allowed the rate constant for myosin degradation to be calculated on successive days after coarctation. The best fit to the observed changes in myosin content was obtained when degradation was increased with the increase in synthesis; when degradation was assumed to be unchanged from sham-operated animals or was decreased, myosin content was overestimated. Moreover, these calculations showed that decay in specific radioactivity of labeled myosin was affected very little even by a large (hundredfold) decrease in degradation. It is concluded that the increased myosin content during development of cardiac hypertrophy is primarily a consequence of increased synthesis.Keywords
This publication has 14 references indexed in Scilit:
- Light Chains of Myosins from White, Red, and Cardiac MusclesProceedings of the National Academy of Sciences, 1971
- Relationship between intracellular amino acids and protein synthesis in the extensor digitorum longus muscle of ratsBiochemical Journal, 1969
- Myocardial DNA synthesis in experimental cardiac hypertrophyAmerican Journal of Physiology-Legacy Content, 1968
- PROTEIN SYNTHESIS DURING WORK-INDUCED GROWTH OF SKELETAL MUSCLEThe Journal of cell biology, 1968
- Effects of actinomycin D and hypophysectomy on development of myocardial hypertrophy in the ratAmerican Journal of Physiology-Legacy Content, 1968
- Myosin Synthesis in Chronic Heart Failure.Experimental Biology and Medicine, 1965
- Myocardial Protein Composition and its Relation to Functional Activity of Varying DegreeCardiology, 1962
- A simple efficient liquid scintillator for counting aqueous solutions in a liquid scintillation counterAnalytical Biochemistry, 1960
- Quantitative studies on the structure of cross-striated myofibrilsBiochimica et Biophysica Acta, 1957