Muinuddin Ahmad, Naqvi Khurram, Sheu Laura, Gaisano Herbert Y, Diamant Nicholas E
Departments of Medicine, University of Toronto, Toronto, Ontario, Canada.
Am J Physiol Gastrointest Liver Physiol. 2005 Jun;288(6):G1233-40. doi: 10.1152/ajpgi.00310.2004. Epub 2005 Feb 3.
Potassium channels are important contributors to membrane excitability in smooth muscles. There are regional differences in resting membrane potential and K(+)-channel density along the length of the feline circular smooth muscle esophagus. The aim of this study was to assess responses of K(+)-channel currents to cholinergic (ACh) stimulation along the length of the feline circular smooth muscle esophageal body. Perforated patch-clamp technique assessed K(+)-channel responses to ACh stimulation in isolated smooth muscle cells from the circular muscle layer of the esophageal body at 2 (distal)- and 4-cm (proximal) sites above the lower esophageal sphincter. Western immunoblots assessed ion channel and receptor expression. ACh stimulation produced a transient increase in outward current followed by inhibition of spontaneous transient outward currents. These ACh-induced currents were abolished by blockers of large-conductance Ca(2+)-dependent K(+) channels (BK(Ca)). Distal cells demonstrated a greater peak current density in outward current than cells from the proximal region and a longer-lasting outward current increase. These responses were abolished by atropine and the specific M(3) receptor antagonist 4-DAMP but not the M(1) receptor antagonist pirenzipine or the M(2) receptor antagonist methoctramine. BK(Ca) expression along the smooth muscle esophagus was similar, but M(3) receptor expression was greater in the distal region. Therefore, ACh can differentially activate a potassium channel (BK(Ca)) current along the smooth muscle esophagus. This activation probably occurs through release of intracellular calcium via an M(3) pathway and has the potential to modulate the timing and amplitude of peristaltic contraction along the esophagus.
钾通道是平滑肌膜兴奋性的重要影响因素。在猫的环形平滑肌食管全长上,静息膜电位和钾通道密度存在区域差异。本研究的目的是评估沿猫环形平滑肌食管体全长,钾通道电流对胆碱能(乙酰胆碱)刺激的反应。穿孔膜片钳技术评估了在下食管括约肌上方2厘米(远端)和4厘米(近端)处食管体环形肌层分离的平滑肌细胞中,钾通道对乙酰胆碱刺激的反应。蛋白质免疫印迹法评估离子通道和受体表达。乙酰胆碱刺激使外向电流短暂增加,随后抑制自发瞬时外向电流。这些乙酰胆碱诱导的电流被大电导钙依赖性钾通道(BKCa)阻滞剂所阻断。远端细胞的外向电流峰值电流密度比近端区域的细胞更大,外向电流增加持续时间更长。这些反应被阿托品和特异性M3受体拮抗剂4 - DAMP阻断,但未被M1受体拮抗剂哌仑西平或M2受体拮抗剂甲溴东莨菪碱阻断。沿平滑肌食管的BKCa表达相似,但M3受体表达在远端区域更高。因此,乙酰胆碱可沿平滑肌食管差异性激活钾通道(BKCa)电流。这种激活可能通过M3途径释放细胞内钙发生,并且有可能调节食管蠕动收缩的时间和幅度。