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自发性高血压大鼠心脏微粒体的特性分析

Characterization of cardiac microsomes from spontaneously hypertonic rats.

作者信息

Heilmann C, Lindl T, Müller W, Pette D

出版信息

Basic Res Cardiol. 1980 Jan-Feb;75(1):92-6. doi: 10.1007/BF02001399.

DOI:10.1007/BF02001399
PMID:6446301
Abstract

Capacity of Ca2+ sequestration was found to be significantly lowered in microsomal preparations of hearts from spontaneously hypertonic rats. A decrease to 40% of the control level was found for basal and extra ATPase. A similar reduction existed in initial and total Ca2+ uptake. These findings are correlated with a lower concentration of the Ca2+ transport ATPase in SDS gel electrophoresis, a lower density of the 7-9 nm intramembraneous particles and higher half-lives of phosphoprotein. Altered contractility of hypertrophied myocardium may thus be partially explained by the dysfunction of the Ca2+ sequestering system.

摘要

自发性高血压大鼠心脏微粒体制剂中Ca2+ 螯合能力显著降低。基础ATP酶和额外ATP酶降低至对照水平的40%。初始Ca2+ 摄取和总Ca2+ 摄取也有类似程度的降低。这些发现与SDS凝胶电泳中Ca2+ 转运ATP酶浓度较低、7-9纳米膜内颗粒密度较低以及磷蛋白半衰期较长相关。因此,肥厚心肌收缩性改变可能部分归因于Ca2+ 螯合系统功能障碍。

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本文引用的文献

1
Myofibrillar adenosine triphosphatase activity in congestive heart failure.充血性心力衰竭时的肌原纤维三磷酸腺苷酶活性
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Comparative ultrastructure and calcium transport in heart and skeletal muscle microsomes.心脏和骨骼肌微粒体的比较超微结构与钙转运
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ATPase activity and Ca 2 ion interaction of myofibrils and sarcoplasmic reticulum isolated from the hearts of spontaneously hypertensive rats.
自发性高血压大鼠心脏中分离出的肌原纤维和肌浆网的ATP酶活性及Ca2+离子相互作用
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Membrane formation by the adenosine triphosphatase of sarcoplasmic reticulum.肌质网三磷酸腺苷酶形成的膜
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Subcellular basis of cardiac contractile failure.
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Molecular transformations in sarcoplasmic reticulum of fast-twitch muscle by electro-stimulation.
Eur J Biochem. 1979 Feb 1;93(3):437-46. doi: 10.1111/j.1432-1033.1979.tb12841.x.
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The reversibility of the sarcoplasmic calcium pump.
Biochim Biophys Acta. 1978 Apr 10;515(1):23-53. doi: 10.1016/0304-4157(78)90007-2.
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ATPase activities, Ca2+ transport and phosphoprotein formation in sarcoplasmic reticulum subfractions of fast and slow rabbit muscles.
Eur J Biochem. 1977 Dec 1;81(2):211-22. doi: 10.1111/j.1432-1033.1977.tb11943.x.