Wu Sheng-Nan, Lin Ming-Wei, Wang Ya-Jean
Department of Physiology, National Cheng Kung University Medical College, No. 1, University Road, Tainan 70101 Taiwan, Republic of China.
Pflugers Arch. 2008 Jan;455(4):687-99. doi: 10.1007/s00424-007-0329-9. Epub 2007 Aug 16.
Di-8-ANEPPS (4-{2-[6-(dibutylamino)-2-naphthalenyl]-ethenyl}-1-(3-sulfopropyl)pyridinium inner salt) has been used as a fast-response voltage-sensitive styrylpyridinium probe. However, little is known regarding the mechanism of di-8-ANEPPS actions on ion currents. In this study, the effects of this dye on ion currents were investigated in pituitary GH(3) cells. In whole-cell configuration, di-8-ANEPPS (10 microM) reversibly increased the amplitude of Ca(2+)-activated K(+) current. In inside-out configuration, di-8-ANEPPS (10 microM) applied to the intracellular surface of the membrane caused no change in single-channel conductance; however, it did enhance the activity of large-conductance Ca(2+)-activated K(+) (BK(Ca)) channels with an EC(50) value of 7.5 microM. This compound caused a left shift in the activation curve of BK(Ca) channels with no change in the gating charge of these channels. A decrease in mean closed time of the channels was seen in the presence of this dye. In the cell-attached mode, di-8-ANEPPS applied on the extracellular side of the membrane also activated BK(Ca) channels. However, neither voltage-gated K(+) nor ether-à-go-go-related gene (erg)-mediated K(+) currents in GH(3) cells were affected by di-8-APPNES. Under current-clamp configuration, di-8-ANEPPS (10 microM) decreased the firing of action potentials in GH(3) cells. In pancreatic betaTC-6 cells, di-8-APPNES (10 microM) also increased BK(Ca)-channel activity. Taken together, this study suggests that during the exposure to di-8-ANEPPS, the stimulatory effects on BK(Ca) channels could be one of potential mechanisms through which it may affect cell excitability.
二辛基-8-苯胺基萘磺酸(4-{2-[6-(二丁基氨基)-2-萘基]-乙烯基}-1-(3-磺丙基)吡啶鎓内盐)已被用作快速响应的电压敏感型苯乙烯基吡啶探针。然而,关于二辛基-8-苯胺基萘磺酸对离子电流的作用机制知之甚少。在本研究中,我们在垂体GH(3)细胞中研究了这种染料对离子电流的影响。在全细胞模式下,二辛基-8-苯胺基萘磺酸(10微摩尔)可逆地增加了钙激活钾电流的幅度。在内外膜外翻模式下,施加于细胞膜内表面的二辛基-8-苯胺基萘磺酸(10微摩尔)对单通道电导没有影响;然而,它确实增强了大电导钙激活钾(BK(Ca))通道的活性,其半数有效浓度(EC(50))值为7.5微摩尔。该化合物使BK(Ca)通道的激活曲线向左移动,而这些通道的门控电荷没有变化。在这种染料存在的情况下,通道的平均关闭时间缩短。在细胞贴附模式下,施加于细胞膜外侧的二辛基-8-苯胺基萘磺酸也激活了BK(Ca)通道。然而,GH(3)细胞中的电压门控钾电流和醚-去极化相关基因(erg)介导的钾电流均不受二辛基-8-苯胺基萘磺酸的影响。在电流钳模式下,二辛基-8-苯胺基萘磺酸(10微摩尔)降低了GH(3)细胞中动作电位的发放频率。在胰腺βTC-6细胞中,二辛基-8-苯胺基萘磺酸(10微摩尔)也增加了BK(Ca)通道的活性。综上所述,本研究表明,在暴露于二辛基-8-苯胺基萘磺酸期间,对BK(Ca)通道产生的刺激作用可能是其影响细胞兴奋性的潜在机制之一。