Kim Jeremy H, Jiang Ya-Ping, Cohen Ira S, Lin Richard Z, Mathias Richard T
Department of Physiology and Biophysics, State University of New York at Stony Brook, Stony Brook, New York, United States of America.
PLoS One. 2017 May 2;12(5):e0176713. doi: 10.1371/journal.pone.0176713. eCollection 2017.
Our previous work on angiotensin II-mediated electrical-remodeling in canine left ventricle, in connection with a long history of other studies, suggested the hypothesis: increases in mechanical load induce autocrine secretion of angiotensin II (A2), which coherently regulates a coterie of membrane ion transporters in a manner that increases contractility. However, the relation between load and A2 secretion was correlative. We subsequently showed a similar or identical system was present in murine heart. To investigate whether the relation between mechanical load and A2-mediated electrical remodeling was causal, we employed transverse aortic constriction in mice to subject the left ventricle to pressure overload for short-term (1 to 2 days) or long-term (1 to 2 weeks) periods. Heart-to-body weight ratios and cell capacitance measurements were used to determine hypertrophy. Whole-cell patch clamp recordings of the predominant repolarization currents Ito,fast and IK,slow were used to assess electrical remodeling. Hearts or myocytes subjected to long-term load displayed significant hypertrophy, which was not evident in short-term load. However, short-term load induced significant reductions in Ito,fast and IK,slow. Incubation of these myocytes with the angiotensin II type 1 receptor inhibitor saralasin for 2 hours restored Ito,fast and IK,slow to control levels. The number of Ito.fast or IK,slow channels did not change with A2 or long-term load, however the hypertrophic increase in membrane area reduced the current densities for both channels. For Ito,fast but not IK,slow there was an additional reduction that was reversed by inhibition of angiotensin receptors. These results suggest increased load activates an endogenous renin angiotensin system that initially reduces Ito,fast and IK,slow prior to the onset of hypertrophic growth. However, there are functional interactions between electrical and anatomical remodeling. First, hypertrophy tends to reduce all current densities. Second, the hypertrophic program can modify signaling between the angiotensin receptor and target current.
我们之前关于犬左心室中血管紧张素 II 介导的电重构的研究,结合其他研究的悠久历史,提出了一个假设:机械负荷增加会诱导血管紧张素 II(A2)的自分泌,它以增加收缩力的方式协同调节一系列膜离子转运体。然而,负荷与 A2 分泌之间的关系是相关性的。我们随后表明,小鼠心脏中存在类似或相同的系统。为了研究机械负荷与 A2 介导的电重构之间的关系是否为因果关系,我们对小鼠进行了横向主动脉缩窄,使左心室在短期(1 至 2 天)或长期(1 至 2 周)内承受压力过载。通过心脏与体重比和细胞电容测量来确定肥大。使用全细胞膜片钳记录主要的复极化电流 Ito,fast 和 IK,slow 来评估电重构。长期负荷的心脏或心肌细胞显示出明显的肥大,短期负荷则不明显。然而,短期负荷会导致 Ito,fast 和 IK,slow 显著降低。用血管紧张素 II 1 型受体抑制剂沙拉新孵育这些心肌细胞 2 小时可使 Ito,fast 和 IK,slow 恢复到对照水平。Ito.fast 或 IK,slow 通道的数量不会随 A2 或长期负荷而改变,然而膜面积的肥大增加降低了这两种通道的电流密度。对于 Ito,fast 而非 IK,slow,存在额外的降低,这种降低可通过抑制血管紧张素受体来逆转。这些结果表明,负荷增加会激活内源性肾素血管紧张素系统,该系统在肥大生长开始之前最初会降低 Ito,fast 和 IK,slow。然而,电重构和解剖学重构之间存在功能相互作用。首先,肥大倾向于降低所有电流密度。其次,肥大程序可以改变血管紧张素受体与目标电流之间的信号传导。