Effects of chronic growth hormone hypersecretion on intrinsic contractility, energetics, isomyosin pattern, and myosin adenosine triphosphatase activity of rat left ventricle.
Effects of chronic growth hormone hypersecretion on intrinsic contractility, energetics, isomyosin pattern, and myosin adenosine triphosphatase activity of rat left ventricle.
复制标题
慢性生长激素分泌过多对大鼠左心室内在收缩力、能量学、异肌球蛋白模式和肌球蛋白三磷酸酶活性的影响。
DOI:
10.1172/jci114737
复制
发表时间:
1990
期刊:
影响因子:
--
通讯作者:
Mercadier,JJ
中科院分区:
文献类型:
--
作者:
Timsit,J;Riou,B;Bertherat,J;Wisnewsky,C;Kato,NS;Weisberg,AS;Lubetzki,J;Lecarpentier,Y;Winegrad,S;Mercadier,JJ
We studied papillary muscle mechanics and energetics, myosin phenotype, and ATPase activities in left ventricles from rats bearing a growth hormone (GH)--secreting tumor. 18 wk after tumor induction, animals exhibited a dramatic increase in body weight (+101% vs. controls) but no change in the ventricular weight/body weight ratio. The maximum isometric force of papillary muscles normalized per cross-sectional area rose markedly (+42%, P less than 0.05 vs. controls), whereas the maximum unloaded shortening velocity did not change. This was observed despite a marked isomyosin shift towards V3 (32 +/- 5% vs. 8 +/- 2% in controls, P less than 0.001). Increased curvature of the force-velocity relationship (+64%, P less than 0.05 vs. controls) indicated that the muscles contracted more economically, suggesting the involvement of V3 myosin. Total calcium- and actin-activated myosin ATPase activities assayed on quickly frozen left ventricular sections were similar in tumor-bearing rats and in controls. After alkaline preincubation, these activities only decreased in tumor-bearing rats, demonstrating that V3 enzymatic sites were involved in total ATPase activity. These data demonstrate that chronic GH hypersecretion in the rat leads to a unique pattern of myocardial adaptation which allows the muscle to improve its contractile performance and economy simultaneously, thanks to myosin phenoconversion and an increase in the number of active enzymatic sites.Images
登录
查看更多内容
影响因子:
5
作者:
Gilbert,PL;Siegel,RJ;Melmed,S;Sherman,CT;Fishbein,MC
通讯作者:
Fishbein,MC
DOI:
10.1677/joe.0.0850075
发表时间:
1980
期刊:
The Journal of endocrinology
影响因子:
--
作者:
R. A. Prysor;J. Jenkins
通讯作者:
J. Jenkins
影响因子:
37.8
作者:
James B. Martins;R. Kerber;B. Sherman;M. Marcus;J. Ehrhardt
通讯作者:
J. Ehrhardt
影响因子:
20.1
作者:
GORZA, L;PAULETTO, P;SCHIAFFINO, S
通讯作者:
SCHIAFFINO, S
DOI:
10.1152/ajpheart.1986.250.6.h1008
发表时间:
1986
期刊:
The American journal of physiology
影响因子:
--
作者:
D. Chemla;Y. Lecarpentier;J. Martín;M. Clergue;A. Antonetti;P. Hatt
通讯作者:
P. Hatt