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Am J Physiol Gastrointest Liver Physiol 289: G501-G507, 2005. First published May 26, 2005; doi:10.1152/ajpgi.00140.2005
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LIVER AND BILIARY TRACT

Identification of a spontaneously active, Na+-permeable channel in guinea pig gallbladder smooth muscle

Georgi V. Petkov,1 Onesmo B. Balemba,2 Mark T. Nelson,1 and Gary M. Mawe1,2

Departments of 1Pharmacology and 2Anatomy and Neurobiology, College of Medicine, University of Vermont, Burlington, Vermont

Submitted 28 March 2005 ; accepted in final form 24 May 2005

The action potential in gallbladder smooth muscle (GBSM) is caused by Ca2+ entry through voltage-dependent Ca2+ channels (VDCC), which contributes to the GBSM contractions. Action potential generation in GBSM is critically dependent on the resting membrane potential (about –50 mV), which is ~35 mV more positive of the K+ equilibrium potential. We hypothesized that a tonic, depolarizing conductance is present in GBSM and contributes to the regulation of the resting membrane potential and action potential frequency. GBSM cells were isolated from guinea pig gallbladders, and the whole cell patch-camp technique was used to record membrane currents. After eliminating the contribution of VDCC and K+ channels, we identified a novel spontaneously active cation conductance (Icat) in GBSM. This Icat was mediated predominantly by influx of Na+. Na+ substitution with N-methyl-D-glucamine (NMDG), a large relatively impermeant cation, caused a negative shift in the reversal potential of the ramp current and reduced the amplitude of the inward current at –50 mV by 65%. Membrane potential recordings with intracellular microelectrodes or in current-clamp mode of the patch-clamp technique indicated that the inhibition of Icat conductance by NMDG is associated with membrane hyperpolarization and inhibition of action potentials. Extracellular Ca2+, Mg2+, and Gd3+ attenuated the Icat in GBSM. Muscarinic stimulation did not activate the Icat. Our results indicate that, in GBSM, an Na+-permeable channel contributes to the maintenance of the resting membrane potential and action potential generation and therefore plays a critical role in the regulation of GBSM excitability and contractility.

nonselective cation channel; motility



Address for reprint requests and other correspondence: G. V. Petkov, Dept. of Pharmacology, Univ. of Vermont, Given Bldg., Rm. B-331, 89 Beaumont Ave., Burlington, VT 05405-0068 (e-mail: Georgi.Petkov{at}uvm.edu)




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