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LIVER AND BILIARY TRACT
Departments of 1Anatomy and Neurobiology and 2Pharmacology, University of Vermont, Burlington, Vermont
Submitted 20 January 2006 ; accepted in final form 21 April 2006
Intracellular Ca2+ waves and spontaneous transient depolarizations were investigated in gallbladder smooth muscle (GBSM) whole mount preparations with intact mucosal layer [full thickness (FT)] by laser confocal imaging of intracellular Ca2+ and voltage recordings with microelectrodes, respectively. Spontaneous Ca2+ waves arose most often near the center, but sometimes from the extremities, of GBSM cells. They propagated regeneratively by Ca2+-induced Ca2+ release involving inositol 1,4,5-trisphosphate [Ins(1,4,5)P3] receptors and were not affected by TTX and atropine (ATS). Spontaneous Ca2+ waves and spontaneous transient depolarizations were more prevalent in FT than in isolated muscularis layer preparations and occurred with similar pattern in GBSM bundles. Ca2+ waves were abolished by the Ins(1,4,5)P3 receptor inhibitors 2-aminoethoxydiphenyl borate and xestospongin C and by caffeine and cyclopiazonic acid. These events were reduced by voltage-dependent calcium channels (VDCCs) inhibitors diltiazem and nifedipine, by PLC inhibitor U-73122, and by thapsigargin and ryanodine. ACh, CCK, and carbachol augmented Ca2+ waves and induced Ca2+ flashes. The actions of these agonists were inhibited by U-73122. These results indicate that in GBSM, discharge and propagation of Ca2+ waves depend on sarco(endo)plasmic reticulum (SR) Ca2+ release via Ins(1,4,5)P3 receptors, PLC activity, Ca2+ influx via VDCCs, and SR Ca2+ concentration. Neurohormonal enhancement of GBSM excitability involves PLC-dependent augmentation and synchronization of SR Ca2+ release via Ins(1,4,5)P3 receptors. Ca2+ waves likely reflect the activity of a fundamental unit of spontaneous activity and play an important role in the excitability of GBSM.
motility; sarcoplasmic reticulum; calcium transients; transient depolarizations; pacemaker; slow waves; action potentials
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