Effects of Hypertrophy and Allylamine-induced Fibrosis on Mechanical Properties of Isolated Rat Heart Muscles with References to the Pumping Function of the Intact Heart in the Same Models : SYMPOSIUM ON LONG-TERM MYOCARDIAL CHANGES IN HEART DISEASES : 49
スポンサーリンク
概要
- 論文の詳細を見る
To examine the effects of hypertrophy and fibrosis on myocardial mechanics, we studied isolated left ventricular papillary muscles from 6-month-old male SHR and allylamine-fed rats. In SHR, the peak developed tension (DT) and the maximum rate of tension development (dT/dt) were higher compared to control male Wistar-Kyoto rats (WKY). With 15 min of hypoxia, the DT and the dT/dt declined similarly in both groups and the ratios of DT and dT/dt to their prehypoxic values after 15 min of hypoxia were not different in the two groups. From allylamine-fed rats, only 4 papillary muscles had more than 25% interstitial fibrosis by point-counting (AL-B group), but 9 muscles had no fibrotic involvement and their left ventricular hydroxyproline concentration was normal (AL-A group). The myocardial diameters, the passive stiffness constant and the duration of isometric contractions at Lmax were increased in AL-B group, but the resting tension, the DT at Lmax and the force-velocity relations did not differ from controls. The mechanical properties of the AL-A group muscles were not different from controls. However, when pumping function was examined in the intact heart from the AL-A group, the LVEDP was increased and the peak cardiac output normalized by body weight was decreased. Thus, hypertrophied muscle from SHR shows hyperfunction without an increase in susceptibility to hypoxic stress. Even if fibrosis progresses, hypertrophy can compensate for the reduction in contractile component up to a certain degree. The dissociation of the results between the isolated heart muscle study and the hemodynamics of the non-fibrotic heart from allylamine-fed rats may indicate the importance of impaired myocardial perfusion for the genesis of heart failure, since allylamine is known to damage medium-size coronary vessels.
- 社団法人日本循環器学会の論文
- 1986-10-20
著者
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KAWAI CHUICHI
The Third Division, Department of lnternal Medicine, Kyoto University Hospital
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NAKAMURA YASUYUKI
The Third Division, Department of Internal Medicine, Faculty of Medicine
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Kawai Chuichi
The Third Division Department Of Internal Medicine. Faculty Of Medicine Kyoto University
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BlNG Oscar
Department of Medicine. Harvard Medical School and the Beth Israel Hospital
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WIEGNER ALLEN
Department of Medicine. Harvard Medical School and the Beth Israel Hospital
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KONISHI Takashi
The Third Division, Department of Internal Medicine. Faculty of Medicine, Kyoto University
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APSTEIN Carl
Department of Medicine, Boston University School of Medicine
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PFEFFER Marc
Department of Medicine, Harvard Medical School and Brigham and Women's Hospital
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Pfeffer Marc
Department Of Medicine Harvard Medical School And Brigham And Women's Hospital
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Konishi T
The Third Division Department Of Internal Medicine. Faculty Of Medicine Kyoto University
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Konishi Takashi
The Third Division Department Of Internal Medicine. Faculty Of Medicine Kyoto University
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Nakamura Yasuyuki
The Third Division Department Of Internal Medicine Faculty Of Medicine
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Nakamura Yasuyuki
The Third Division Department Of Internal Medicine. Faculty Of Medicine Kyoto University
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Kawai Chuichi
The Third Department Of Internal Medicine Faculty Of Medicine Kyoto University
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Apstein Carl
Department Of Medicine Boston University School Of Medicine
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Nakamura Y
Second Department Of Internal Medicine Kyoto Prefectural University Of Medicine
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