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代谢和循环紊乱动物心脏钙释放单位的形态特征。

Morphological characteristics of cardiac calcium release units in animals with metabolic and circulatory disorders.

机构信息

Department of Physiological Sciences, National Institute of Fitness and Sports, Kanoya, Kagoshima, Japan.

出版信息

J Muscle Res Cell Motil. 2009;30(5-6):225-31. doi: 10.1007/s10974-009-9191-z. Epub 2009 Nov 19.

Abstract

Metabolic and circulatory disorders such as diabetes and hypertension are associated with cardiac dysfunction. Research on these types of experimental animals has observed abnormal calcium (Ca(2+)) sparks and waves in cells; a potential mechanism altering excitation-contraction (e-c) coupling in the myocardium. The e-c coupling depends on the intricate spatial relationship between the sarcolemma and sarcoplasmic reticulum calcium release units (CRU's). The objective of this study was to assess for a presence or absence of abnormalities in CRU's from type II diabetic and hypertensive rat models. Myocardial tissue underwent perfusion fixation followed by selective staining of the CRU's and the features observed using a high voltage electron microscope. Results revealed both diabetic groups had significant increases in body weight, a tendency toward an enlarged heart, and a significant disruption of the CRU's and displacement of transverse (t)-tubules in a longitudinal direction. The hypertensive model characteristically showed a dramatic increase in heart size, a significant increase in disrupted CRU's and a tendency towards longitudinal t-tubule orientation. We propose the two disorders of diabetes and hypertension have a similar etiology of cardiomyopathy resulting, in part, from an increase in the number of incomplete CRU's, due to a morphological change in the architecture and orientation of the t-tubules. These architectural changes could potentially explain the impaired calcium signaling previously observed in diabetic and hypertensive cardiomyopathy.

摘要

代谢和循环紊乱,如糖尿病和高血压,与心脏功能障碍有关。对这些类型的实验动物的研究观察到细胞中异常的钙(Ca(2+))火花和波;这是一种改变心肌兴奋-收缩(e-c)偶联的潜在机制。e-c 偶联依赖于肌膜和肌浆网钙释放单元(CRU)的复杂空间关系。本研究的目的是评估 II 型糖尿病和高血压大鼠模型中 CRU 是否存在异常。心肌组织进行灌流固定,然后选择性地对 CRU 进行染色,并用高电压电子显微镜观察观察到的特征。结果表明,两组糖尿病大鼠体重均显著增加,心脏有增大趋势,CRU 明显受损,横(t)小管沿长轴方向移位。高血压模型的特点是心脏明显增大,CRU 严重受损,t 小管有纵向取向的趋势。我们提出,糖尿病和高血压这两种疾病具有相似的心肌病病因,部分原因是由于 t 小管的结构和取向发生形态变化,导致不完全 CRU 的数量增加。这些结构变化可能可以解释先前在糖尿病和高血压性心肌病中观察到的钙信号受损。

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