4.7 Article

Low-voltage-activated inward current in murine antral smooth muscle cells is an artifact

期刊

AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
卷 320, 期 4, 页码 C966-C973

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpcell.00031.2021

关键词

A-type K+ currents; smooth muscle cells; T-type Ca2+ currents

资金

  1. National Institutes of Health/National Institute of Diabetes and Digestive and Kidney Grant [P01-DK41315]
  2. National Institutes of Health/National Institute of General Medical Sciences [P20-GM130459]

向作者/读者索取更多资源

In murine antral smooth muscle cells, low-voltage-activated inward currents are generated by K+ influx via KA channels, rather than T-type Ca2+ channels, Ca2+-activated Cl- channels, or nonselective cation channels.
Two types of voltage-dependent inward currents were evoked by depolarization in murine antral smooth muscle cells (SMCs) bathed in Ca2+-containing physiological solution: high-voltage-activated (HVA) and low-voltage-activated (LVA) inward currents. We examined whether the LVA current was due to: 1) T-type Ca2+ channels, 2) Ca2+-activated Cl- channels, 3) nonselective cation channels (NSCC), or 4) voltage-dependent K+ channels. Replacement of external Ca2+ (2 mM) with equimolar Ba2+ increased the amplitude of the HVA current but blocked the LVA current. Nicardipine blocked the HVA current, and in the presence of nicardipine, T-type Ca2+ blockers failed to block LVA current. A Cl- channel antagonist had little effect on LVA current. Cation-free external solution completely abolished both HVA and LVA currents. Addition of Ca2+ to the solution restored only HVA currents. Addition of K+ (5 mM) to otherwise cation-free solution induced LVA current that reversed at similar to 20 mV. These data suggest that LVA current is not due to T-type Ca2+ channels, Ca2+-activated Cl- channels, or NSCC. A-type K+ (KA) currents and delayed rectifying K+ (K-DR) currents can be resolved in antral SMCs dialyzed with a solution containing 140mM K+. When cells were exposed to high K+ external solution and dialyzed with Cs+-rich solution in the presence of nicardipine, LVA current was evoked and reversed at positive potentials. LVA currents were blocked by K+ channel blockers, 4-aminopyridine, and tetraethylammonium. In conclusion, LVA inward currents can be generated by K+ influx via KA channels in murine antral SMCs when cells were dialyzed with Cs+-rich solution.

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