Park M K, Lee S H, Ho W K, Earm Y E
Department of Physiology, Dankook University College of Medicine, Anseo-Dong, Chunan, Korea.
Exp Physiol. 1995 Sep;80(5):835-42. doi: 10.1113/expphysiol.1995.sp003891.
Ca(2+)-activated K+ currents (IK(Ca)) and voltage-dependent Ca(2+)-insensitive K+ currents (IK(V)) were recorded using the patch clamp technique to study the pulmonary (PASMC) and ear arterial smooth muscle cells (EASMC) of the rabbit and the possible regulatory mechanisms related to hypoxia. When a hypoxic solution (1 mM Na2S2O4, gassed with 100% N2) was superfused, the activity of Ca(2+)-activated K+ channels (KCa channels) recorded at a pipette potential of -70 mV in cell-attached mode was decreased to 49 +/- 7% in PASMC, whereas EASMC KCa channels did not respond to hypoxia. In inside-out patches (bathed symmetrically in 150 mM KCl), reducing agents such as dithiothreitol (DTT; 5 mM), reduced glutathione (GSH; 5 mM) and NADH (2 mM) decreased KCa channel activity in PASMC, but they did not affect the EASMC KCa channel. However, oxidizing agents such as 5,5'-dithio-bis(2-nitrobenzoic acid) (DTNB; 1 mM), oxidized GSH (GSSG; 5 mM) and NAD (2 mM) increased KCa channel activity in both PASMC and EASMC. In the whole-cell configuration, using a pipette solution containing a high concentration of 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid (BAPTA; 10 mM), PASMC IK(V) were activated by depolarizing step pulses to voltages more positive than -30 mV (holding potential, -80 mV). IK(V) was increased by application of a membrane-permeable oxidizing agent, 2,2'-dithio-bis(5-nitropyridine) (DTBNP; 200 microM), whereas it was decreased by application of DTT (5 mM). From these results, it could be suggested that hypoxic pulmonary vasoconstriction is attributable, at least in part, to a change of cellular redox state, which decreases outward K+ currents. This hypothesis is further supported by the observation that the basal redox state of EASMC KCa channels is more reduced than that of PASMC KCa channels. The distinct responses to hypoxia of pulmonary and systemic arterial smooth muscle could be explained by this difference.
采用膜片钳技术记录兔肺动脉平滑肌细胞(PASMC)和耳动脉平滑肌细胞(EASMC)中的钙激活钾电流(IK(Ca))和电压依赖性钙不敏感钾电流(IK(V)),并研究与缺氧相关的可能调节机制。当用缺氧溶液(1 mM Na2S2O4,用100% N2通气)灌流时,在细胞贴附模式下,于-70 mV的电极电位记录的钙激活钾通道(KCa通道)活性在PASMC中降至49±7%,而EASMC的KCa通道对缺氧无反应。在向外膜片(对称浸泡于150 mM KCl中)中,二硫苏糖醇(DTT;5 mM)、还原型谷胱甘肽(GSH;5 mM)和NADH(2 mM)等还原剂可降低PASMC中KCa通道的活性,但对EASMC的KCa通道无影响。然而,5,5'-二硫代双(2-硝基苯甲酸)(DTNB;1 mM)、氧化型谷胱甘肽(GSSG;5 mM)和NAD(2 mM)等氧化剂可增加PASMC和EASMC中KCa通道的活性。在全细胞模式下,使用含有高浓度1,2-双(2-氨基苯氧基)乙烷-N,N,N',N'-四乙酸(BAPTA;10 mM)的电极内液,通过将去极化阶跃脉冲施加到比-30 mV更正的电压(保持电位为-80 mV)来激活PASMC的IK(V)。应用膜通透性氧化剂2,2'-二硫代双(5-硝基吡啶)(DTBNP;200 microM)可增加IK(V),而应用DTT(5 mM)则使其降低。从这些结果可以推测,缺氧性肺血管收缩至少部分归因于细胞氧化还原状态的改变,这种改变会减少外向钾电流。EASMC的KCa通道的基础氧化还原状态比PASMC的KCa通道的基础氧化还原状态更还原,这一观察结果进一步支持了该假设。肺和体动脉平滑肌对缺氧的不同反应可以用这种差异来解释。