Unno T, Inaba T, Ohashi H, Takewaki T, Komori S
Department of Veterinary Medicine, Faculty of Agriculture, United Graduate School, Gifu University, Japan.
Jpn J Pharmacol. 2000 Dec;84(4):431-7. doi: 10.1254/jjp.84.431.
In single smooth muscle cells dispersed from guinea pig ileum, the muscarinic agonist carbachol (CCh) at 2 microM produced an oscillatory or sustained type of depolarization and at 100 microM, the latter type depolarization. Depletion of internal Ca2+ stores blocked the oscillatory response, but not the sustained responses to 2 microM and 100 microM CCh, although their decay after reaching the peak became faster. Blocking voltage-dependent Ca2+ channels (VDCCs) blocked both types of response to 2 microM CCh, but only slowed the initial rising phase of 100 microM CCh responses. Combination of Ca2+ store depletion and VDCC blockade abolished the responses to 2 microM CCh again and decreased those to 100 microM CCh in peak amplitude and persistency. Combination of Ca2+ store depletion with removal of extracellular Ca2+ markedly reduced or abolished the 100 microM CCh responses. The results suggest that muscarinic depolarization of the ileal cells requires Ca2+ mobilization for its generation and persistence; at weak muscarinic stimulation, both Ca2+ entry via VDCCs and Ca2+ release from internal stores may contribute to the Ca2+ mobilization; and under strong muscarinic stimulation, Ca2+ entry pathways resistant to VDCC blockers may also contribute to it.
在从豚鼠回肠分离出的单个平滑肌细胞中,2微摩尔的毒蕈碱激动剂卡巴胆碱(CCh)产生振荡性或持续性去极化,而在100微摩尔时,则产生后一种类型的去极化。细胞内钙库耗竭可阻断振荡性反应,但不能阻断对2微摩尔和100微摩尔CCh的持续性反应,尽管它们在达到峰值后的衰减变得更快。阻断电压依赖性钙通道(VDCCs)可阻断对2微摩尔CCh的两种反应类型,但仅减缓100微摩尔CCh反应的初始上升阶段。钙库耗竭与VDCC阻断相结合,再次消除了对2微摩尔CCh的反应,并降低了对100微摩尔CCh反应的峰值幅度和持续性。钙库耗竭与去除细胞外钙相结合,显著降低或消除了100微摩尔CCh反应。结果表明,回肠细胞的毒蕈碱去极化需要钙动员来产生和维持;在弱毒蕈碱刺激下,通过VDCCs的钙内流和从细胞内钙库释放的钙都可能有助于钙动员;在强毒蕈碱刺激下,对VDCC阻滞剂有抗性的钙内流途径也可能有助于钙动员。