Role of Ca2+ Mobilization in Muscarinic Receptor-Mediated Membrane Depolarization in Guinea Pig Ileal Smooth Muscle Cells

The Japanese Journal of Pharmacology

Hidenori Ohashi¹  Tadafumi Inaba¹  Toshihiro Unno¹  Tadashi Takewaki²  Seiichi Komori¹ 

[1] Laboratory of Pharmacology, Department of Veterinary Medicine, Faculty of Agriculture, United Graduate School, Gifu University, 1-1 Yanagido, Gifu 501-1193, Japan;Department of Pathogenetic Veterinary Science, United Graduate School, Gifu University, 1-1 Yanagido, Gifu 501-1193, Japan

关键词: Intestinal smooth muscle;    Muscarinic receptor;    Membrane potential;    Ca2+ mobilization;    Ca2+ store;   

DOI  :  10.1254/jjp.84.431

学科分类：药理学

来源: Nihon Yakuri Gakkai Henshuubu / Japanese Pharmacological Society

【 摘 要 】

References(24)Cited-By(8)In single smooth muscle cells dispersed from guinea pig ileum, the muscarinic agonist carbachol (CCh) at 2μM produced an oscillatory or sustained type of depolarization and at 100μM, the latter type depolarization. Depletion of internal Ca2+ stores blocked the oscillatory response, but not the sustained responses to 2μM and 100μM CCh, although their decay after reaching the peak became faster. Blocking voltage-dependent Ca2+ channels (VDCCs) blocked both types of response to 2μM CCh, but only slowed the initial rising phase of 100μM CCh responses. Combination of Ca2+ store depletion and VDCC blockade abolished the responses to 2μM CCh again and decreased those to 100μM CCh in peak amplitude and persistency. Combination of Ca2+ store depletion with removal of extracellular Ca2+ markedly reduced or abolished the 100μM 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.

【 授权许可】

Unknown