Tanahashi Yasuyuki, Ichimura Yoshirou, Kimura Kaori, Matsuyama Hayato, Iino Satoshi, Komori Seiichi, Unno Toshihiro
Department of Animal Medical Sciences, Faculty of Life Sciences, Kyoto Sangyo University, Motoyama, Kamigamo, Kita-Ku, Kyoto, 603-8555, Japan,
Naunyn Schmiedebergs Arch Pharmacol. 2014 Apr;387(4):377-88. doi: 10.1007/s00210-013-0944-2. Epub 2013 Dec 10.
To elucidate the roles played by the interstitial cells of Cajal in the myenteric layer (ICC-MY) in cholinergic neuromuscular transmission, we recorded mechanical and electrical activities in response to electrical field stimulation (EFS) of the ileal longitudinal muscle strips from WBB6F1-W/W(V) (W/W(V)) mutant mice, that lacked ICC-MY and compared with those in WBB6F1-+/+ (+/+) control mice. In +/+ muscle strips, EFS induced phasic contractions, which were abolished or strongly attenuated by atropine or tetrodotoxin. In W/W(V) preparations, EFS induced similar phasic contractions, but the cholinergic component was smaller than that in +/+ strips. This was despite of the fact that the contractions because of exogenous applications of carbachol and high K(+) solution in W/W(V) strips were comparable to or rather greater than those in the +/+ preparations. EFS induced atropine-sensitive excitatory junction potentials (EJPs) in the +/+ longitudinal smooth muscle cells but not in W/W(V) cells. In the presence of eserine, EFS induced atropine-sensitive EJPs in W/W(V) cells. These results suggest that ICC-MY mediate the cholinergic neuromuscular transmission in mouse ileal longitudinal smooth muscles. In addition, the other pathway in which ICC-MY are not involved can operate concomitantly.
为了阐明肌间层Cajal间质细胞(ICC-MY)在胆碱能神经肌肉传递中的作用,我们记录了来自缺乏ICC-MY的WBB6F1-W/W(V)(W/W(V))突变小鼠回肠纵肌条对电场刺激(EFS)的机械和电活动,并与WBB6F1-+/+(+/+)对照小鼠进行比较。在+/+肌条中,EFS诱导相性收缩,阿托品或河豚毒素可消除或强烈减弱这种收缩。在W/W(V)标本中,EFS诱导相似的相性收缩,但胆碱能成分比+/+肌条中的小。尽管W/W(V)肌条中外源性应用卡巴胆碱和高钾溶液引起的收缩与+/+标本中的相当或更大。EFS在+/+纵行平滑肌细胞中诱导阿托品敏感的兴奋性接头电位(EJP),但在W/W(V)细胞中未诱导。在存在毒扁豆碱的情况下,EFS在W/W(V)细胞中诱导阿托品敏感的EJP。这些结果表明,ICC-MY介导小鼠回肠纵行平滑肌中的胆碱能神经肌肉传递。此外,ICC-MY不参与的其他途径可以同时起作用。