Viola H M, Macdonald W A, Tang H, Hool L C
The University of Western Australia and The Western Australian Institute for Medical Research, Crawley, Western Australia.
Curr Med Chem. 2009;16(26):3341-58. doi: 10.2174/092986709789057671. Epub 2009 Sep 1.
The L-type Ca(2+) channel plays a critical role in cardiac function as the main route for entry of calcium into cardiac myocytes. It is essential to excitability as it shapes the long plateau phase of the cardiac action potential that is unique to cardiac ventricular myocytes. It is necessary for contraction as it triggers the release of calcium from sarcoplasmic reticulum stores for actin-myosin interaction. The L-type Ca(2+) channel also regulates cytoplasmic calcium levels. It is well recognised that an increase in intracellular calcium is involved in the activation of growth-promoting signal pathways. Recently reactive oxygen species have been implicated in the activation of signal pathways and the development of pathological hypertrophy. There is now evidence that implicates activation of the L-type Ca(2+) channel with persistent alterations in calcium homeostasis and cellular reactive oxygen species production as a possible trigger of cardiac hypertrophy. A number of different approaches have been used to modify channel function with the view to preventing ischemia-reperfusion injury, cardiac hypertrophy or cardiac failure providing good evidence that the L-type Ca(2+) channel may be an efficacious target in the prevention of cardiac pathology.
L型Ca(2+)通道作为钙进入心肌细胞的主要途径,在心脏功能中起着关键作用。它对兴奋性至关重要,因为它塑造了心室肌细胞特有的心脏动作电位的长平台期。它对收缩是必需的,因为它触发肌浆网钙库释放钙以进行肌动蛋白-肌球蛋白相互作用。L型Ca(2+)通道还调节细胞质钙水平。众所周知,细胞内钙增加参与促进生长的信号通路的激活。最近,活性氧与信号通路的激活和病理性肥大的发展有关。现在有证据表明,L型Ca(2+)通道的激活以及钙稳态和细胞活性氧产生的持续改变可能是心脏肥大的触发因素。为了预防缺血-再灌注损伤、心脏肥大或心力衰竭,人们采用了多种不同方法来改变通道功能,这充分证明L型Ca(2+)通道可能是预防心脏病理的有效靶点。