Na+ channel inactivation: a comparative study between pancreatic islet beta-cells and adrenal chromaffin cells in rat. J Physiol 2003 Apr 01;548(Pt 1):191-202
Date
02/11/2003Pubmed ID
12576496Pubmed Central ID
PMC2342793DOI
10.1113/jphysiol.2002.034405Scopus ID
2-s2.0-0037385010 (requires institutional sign-in at Scopus site) 33 CitationsAbstract
A comparative study was carried out on the inactivation of Na+ channels in two types of endocrine cells in rats, beta-cells and adrenal chromaffin cells (ACCs), using patch-clamp techniques. The beta-cells were very sensitive to hyperpolarization; the Na+ currents increased ninefold when the holding potential was shifted from -70 mV to -120 mV. ACCs were not sensitive to hyperpolarization. The half-inactivation voltages were -90 mV (rat beta-cells) and -62 mV (ACCs). The time constant for recovery from inactivation at -70 mV was 10.5 times slower in beta-cells (60 ms) than in ACCs (5.7 ms). The rate of Na+-channel inactivation at physiological resting potential was more than three times slower in beta-cells than in ACCs. Na+ influx through Na+ channels had no effect on the secretory machinery in rat beta-cells. However, these 'silent Na+ channels' could contribute to the generation of action potentials in some conditions, such as when the cell is hyperpolarized. It is concluded that the fractional availability of Na+ channels in beta-cells at a holding potential of -70 mV is about 15 % of that in ACCs. This value in rat beta-cells is larger than that observed in mouse (0 %), but is smaller than those observed in human or dog (90 %).
Author List
Lou XL, Yu X, Chen XK, Duan KL, He LM, Qu AL, Xu T, Zhou ZAuthor
Xuelin Lou PhD Professor in the Cell Biology, Neurobiology and Anatomy department at Medical College of WisconsinMESH terms used to index this publication - Major topics in bold
Adrenal GlandsAnimals
Cells, Cultured
Chromaffin Cells
Electrophysiology
Islets of Langerhans
Kinetics
Membrane Potentials
Mice
Patch-Clamp Techniques
Rats
Rats, Wistar
Sodium Channel Blockers
Tolbutamide