心脏负荷生物学。

Pathobiology annual Pub Date : 1982-01-01
B Swynghedauw, C Delcayre
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引用次数: 0

摘要

心脏的机械负荷引起两种不同类型的适应机制。(a)从定性的角度来看,缩短的最大速度与肌球蛋白同工酶变化有关,导致atp酶减少,尽管从生理学的角度来看松弛是正常的,但肌浆网Ca2+摄取异常的存在已经得到了很好的证明。这两种方法似乎都通过减少每克张力产生的热量来提高效率。动作电位大幅度扩大的存在现已得到充分证实,但在生化水平上仍未得到解释。线粒体的功能是相当有争议的,虽然已经证明它们更丰富和更小,但它们的呼吸指数变化的原因仍然未知。(b)从数量的观点来看,成人心脏通过增加其质量来适应负荷。这主要是肌细胞肥大和非肌细胞有丝分裂增殖的结果。数据表明,至少在人类中,肌细胞无丝分裂可能发生,也可能在非常大的实验性肥大中发生。除了这一现象外,还增加了肌细胞核多倍体的发育,这似乎是某些物种所特有的。蛋白质合成的刺激在压力过载后很快发生,在体积过载时延迟;蛋白质裂解也会增加,尽管这是有争议的。无论蛋白质是什么,这个过程都会发生。这伴随着核活性的增加和RNA合成的刺激,尤其是信使RNA的早熟。在早期可能是蛋白质合成的潜在信号的事件中,人们的注意力集中在多胺、RNA聚合酶和尿嘧啶激酶上。当然,触发机制仍是假设。一些数据表明,作为蛋白质合成的触发因素,壁应力和拉伸会增加;效率的下降被认为是质变的诱因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biology of cardiac overload.

Mechanical overload in the heart induces two different types of adaptational mechanisms. (a) From a qualitative point of view, the maximum speed of shortening is depressed in relation to a myosin isoenzymic change responsible for decreased ATPase and, although the relaxation appears normal from a physiological point of view, the existence of an abnormality in Ca2+ uptake in the sarcoplasmic reticulum has been well documented. Both of these processes appear to improve efficiency by decreasing the heat produced per gram of tension. The existence of a large broadening of the action potential has now been well established, but it remains unexplained at the biochemical level. The functioning of mitochondria is rather controversial, and although it has been shown that they are both more abundant and smaller, the reason why their respiratory index changes remains unknown. (b) From a quantitative point of view, the adult heart adapts to overload by increasing its mass. This is mainly a consequence of a hypertrophy of the myocytes and a mitotic multiplication of nonmuscular cells. Data suggest that myocyte amitotic divisions may occur, at least in humans, and perhaps in very sizeable experimental hypertrophy. To this phenomenon has been added the development of polyploidy of myocyte nuclei, which seems to be specific to certain species. The stimulation of protein synthesis occurs very soon after pressure overload, and is delayed in volume overload; protein lysis also increases, although this is controversial. The process occurs whatever the proteins. This is accompanied by increased nuclear activity and a stimulation in RNA synthesis, which is especially precocious for messenger RNA. Among the very early events which could be potential signals for protein synthesis, attention has been focused on polyamine, RNA polymerase, and uridine kinase. The trigger mechanism, of course remains hypothetical. As a trigger for protein synthesis, several data suggest an increase in wall stress and stretch; a drop in efficiency is suggested as a trigger for qualitative changes.

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