扩张型心肌病的核/细胞质关系改变和退行性结构改变。

Cardioscience Pub Date : 1994-06-01
D Scholz, W Diener, J Schaper
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引用次数: 0

摘要

我们系统地研究了扩张型心肌病患者因顽固性心力衰竭而接受移植的心肌结构。术中取出12例患者(男10例,女2例,年龄31-57岁,射血分数< 20%)的心脏,取大量标本进行光镜和电镜观察。8例房间隔缺损手术中左心室活检作为对照组织。最明显的定性表现为肌细胞局灶性肥大和萎缩,细胞核增大和形状怪异,缺乏可收缩物质,出现大量小线粒体。在定量水平上,核密度降低(18%,p < 0.05),但核剖面面积显著增加(85%,p < 0.001)。因此,细胞核与细胞质的关系发生了改变。收缩丝的体积密度降低(25%,p < 0.001),但线粒体体积密度不变。细胞宽度增加39% (p < 0.01),结缔组织含量(=纤维化)增加112% (p < 0.001)。提示核异常可能是扩张型心肌病发病的主要原因。这可能导致转录率降低,这很可能是肌丝缺失和其他退行性变化的原因。肥大肌细胞结构质量的恶化最终导致萎缩和纤维化,可能是扩张型心肌病功能障碍的结构相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Altered nucleus/cytoplasm relationship and degenerative structural changes in human dilated cardiomyopathy.

We investigated systematically the structure of the myocardium obtained from patients with dilated cardiomyopathy undergoing transplantation because of intractable heart failure. Hearts were explanted at the time of surgery from 12 patients (10 men and 2 women, aged 31-57 years, ejection fraction < 20%) and numerous samples were taken for light and electron microscopy. Biopsies from the left ventricle of 8 patients during operations for atrial septal defect served as control tissue. The most obvious qualitative findings were focal hypertrophy and atrophy of myocytes, enlargement and bizarre shape of nuclei, lack of contractile material and occurrence of numerous small mitochondria. On a quantitative level, the nuclear density was reduced (18%, p < 0.05) but the nuclear profile area was significantly increased (85%, p < 0.001). Thus the nucleus/cytoplasm relationship was altered. The volume density of the contractile filaments was decreased (25%, p < 0.001), but the mitochondrial volume density was unchanged. There was an increase in cell width (39%, p < 0.01) and of the connective tissue content (= fibrosis) (112%, p < 0.001). It is suggested that the nuclear abnormalities may be the primary event in the pathogenesis of dilated cardiomyopathy. These may then lead to a reduced transcriptional rate which most probably is the cause of the lack of myofilaments and other degenerative changes. The deterioration of the structural quality of the hypertrophied myocytes results finally in atrophy and fibrosis and may be the structural correlate of functional disturbances in dilated cardiomyopathy.

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