Cingolani Horacio E, Perez Nestor G, Aiello Ernesto A, Ennis Irene L, Garciarena Carolina D, Villa-Abrille Maria C, Dulce Raul A, Caldiz Claudia I, Yeves Alejandra M, Correa Maria V, Nolly Mariela B, Chiappe de Cingolani Gladys
Centro de Investigaciones Cardiovasculares, Facultad de Ciencias Medicas, Universidad Nacional de La Plata, Calle 60 y 120, 1900 La Plata, Argentina.
Front Biosci. 2008 May 1;13:7096-114. doi: 10.2741/3213.
The enhanced activity of the cardiac Na+/H+ exchanger (NHE-1) after myocardial stretch is considered a key step of the intracellular signaling pathway leading to the slow force response to stretch as well as an early signal for the development of cardiac hypertrophy. We propose that the chain of events triggered by stretch begins with the release of small amounts of Angiotensin II (Ang II)/endothelin (ET) and ends with the increase in intracellular Ca2+ concentration ([Ca2+]i) through the Na+/Ca2+ exchanger in reverse mode (NCX(rev)), which triggers cardiac hypertrophy by activation of widely recognized Ca2+-dependent intracellular signaling pathways.
心肌牵张后心脏钠氢交换体(NHE-1)活性增强被认为是导致对牵张产生缓慢力量反应的细胞内信号通路的关键步骤,也是心脏肥大发展的早期信号。我们提出,牵张引发的一系列事件始于少量血管紧张素II(Ang II)/内皮素(ET)的释放,止于通过反向模式的钠钙交换体(NCX(rev))使细胞内钙离子浓度([Ca2+]i)升高,后者通过激活广泛认可的钙依赖细胞内信号通路触发心脏肥大。