Chatelier A, Imbert N, Infante J L Zambonino, McKenzie D J, Bois P
Université de La Rochelle, Laboratoire de Biologie et Environnement Marin, Avenue Michel Crépeau, 17042, La Rochelle cedex, France.
J Exp Biol. 2006 Oct;209(Pt 20):4033-9. doi: 10.1242/jeb.02470.
The present study employed a patch clamp technique in isolated seabass ventricular myocytes to investigate the hypothesis that oleic acid (OA), a mono-unsaturated fatty acid, can exert direct effects upon whole-cell barium currents. Acute application of free OA caused a dose-dependent depression of the whole-cell barium current that was evoked by a voltage step to 0 mV from a holding potential of -80 mV. The derived 50% inhibitory concentration (IC50) was 12.49+/-0.27 micromol l(-1). At a concentration of 30 micromol l(-1), OA significantly reduced the current density to about 45% of control values, but did not modify either the shape of the current-density voltage relationship or the apparent reversal potential. In addition, OA did not modify the voltage dependence of either steady state inactivation or activation curves. Taken together, these results indicate that physiological concentrations of free OA decrease the conductance of the L-type inward current, without altering its properties of selectivity and its voltage dependence. The inhibitory effect of OA upon the L-type calcium channel may translate, in vivo, into a protective effect against arrhythmias induced by Ca2+ overload.
本研究采用膜片钳技术,对分离的海鲈心室肌细胞进行研究,以验证单不饱和脂肪酸油酸(OA)可直接影响全细胞钡电流这一假设。从 -80 mV 的钳制电位向 0 mV 进行电压阶跃时,急性施加游离 OA 会导致全细胞钡电流呈剂量依赖性降低。得出的 50% 抑制浓度(IC50)为 12.49±0.27 μmol l(-1)。在 30 μmol l(-1) 的浓度下,OA 可使电流密度显著降低至对照值的约 45%,但既不改变电流密度 - 电压关系的形状,也不改变表观反转电位。此外,OA 不会改变稳态失活或激活曲线的电压依赖性。综上所述,这些结果表明,游离 OA 的生理浓度会降低 L 型内向电流的电导,而不会改变其选择性特性及其电压依赖性。OA 对 L 型钙通道的抑制作用在体内可能转化为对 Ca2+ 过载诱导的心律失常的保护作用。