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Single inwardly rectifying potassium channels in cultured muscle cells from rat and mouse.
Author(s) -
Matsuda H,
Stanfield P R
Publication year - 1989
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.1989.sp017679
Subject(s) - pipette , conductance , chemistry , membrane potential , potassium channel , potassium , depolarization , ion channel , analytical chemistry (journal) , patch clamp , biophysics , physics , biochemistry , chromatography , biology , receptor , organic chemistry , condensed matter physics
1. Inward unitary currents through inwardly rectifying K+ channels of myotubes derived from newborn rats or from a murine, clonal myoblast cell line were studied in the cell‐attached configuration. Open‐closed transitions of the channel were observed in the absence of blocking ions. 2. The single‐channel conductance was 26.3 +/‐ 2.9 pS (mean + S.D., n = 14) with 150 mM‐K+ pipette solution at room temperature (19‐22 degrees C). The channel showed substates of conductance in addition to the main conductance state. A channel with a smaller conductance (8.9 +/‐ 2.6 pS, n = 4) was also but less frequently observed. 3. The probability of the channel being open is weakly voltage dependent: it decreased from 0.94 to 0.84 as the membrane was hyperpolarized from the resting potential (RP) + 20 mV to RP ‐ 50 mV. 4. The lifetimes of the openings were distributed according to a single exponential. At least three exponentials were required to fit the frequency histogram of the lifetimes of all closed states. The mean open time showed a weak voltage dependence, while the mean closed times had little voltage dependence. 5. In the presence of external Na+, the open probability decreased from 0.89 to 0.43 and the mean open time decreased from 203 to 28 ms (40 mM‐K+, 200 mM‐Na+ pipette solution) when the patch membrane was hyperpolarized from RP ‐ 40 mV to RP ‐ 110 mV. The mean closed times were not different from those with 150 mM‐K+, Na+‐free pipette solution and showed little voltage dependence. 6. It is suggested that inactivation of the macroscopic inward currents during hyperpolarization results mainly from a voltage‐dependent block by Na+ with relatively slow kinetics.