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New Aspects for the Treatment of Cardiac Diseases Based on the Diversity of Functional Controls on Cardiac Muscles: Diversity in the Excitation–Contraction Mechanisms of the Heart

机译:基于心脏肌肉功能控制多样性的心脏疾病治疗新方面:心脏兴奋收缩机制的多样性

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References(39) Cited-By(13) The waveform of the myocardial action potential (AP) triggering contraction differs among the species, developmental stage, and pathological state. The species difference in heart rate, which inversely correlates with body size, originates in the ion-channel mechanisms responsible for diastolic depolarization of the sinoatrial node. In some cases, such as the chronically AV-blocked dog and 11- to 13-day chick embryo, the repolarization reserve is decreased making the heart useful for drug evaluation. The degree of dependence of contraction on sarcoplasmic reticulum (SR) function increases during development. The large SR dependence and short AP of the adult mouse and rat support their rapid contraction under high heart rate. The function of the Na+/Ca2+ exchanger is affected by AP waveform and ion concentrations; its major role is Ca2+ extrusion, but under pathological conditions such as ischemia-reperfusion, it allows Ca2+ influx and leads to myocardial injury, including loss of mitochondrial function. The role of mitochondria in ATP supply is less in the fetus where glycolysis plays a greater role. The pharmacological properties of the myocardium are affected by all of these factors and also by autonomic innervation and the hormonal status. Such comprehensive understanding is indispensable for the development of novel therapeutic strategies.
机译:参考文献(39)被引用(13)触发收缩的心肌动作电位(AP)的波形在物种,发育阶段和病理状态之间有所不同。心率的物种差异与体型成反比,其起因于负责窦房结舒张性去极化的离子通道机制。在某些情况下,例如慢性AV阻滞犬和11到13天的雏鸡胚胎,复极储备减少,从而使心脏可用于药物评估。收缩对肌浆网(SR)功能的依赖程度在发育过程中增加。成年小鼠和大鼠的较大SR依赖性和较短的AP支持在高心率下快速收缩。 Na + / Ca2 +交换剂的功能受AP波形和离子浓度的影响;它的主要作用是促进Ca2 +的排出,但在诸如缺血再灌注等病理条件下,它会使Ca2 +大量涌入并导致心肌损伤,包括线粒体功能丧失。在糖酵解作用较大的胎儿中,线粒体在ATP供应中的作用较少。心肌的药理特性受所有这些因素以及植物神经支配和激素状态的影响。这种全面的理解对于开发新的治疗策略必不可少。

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