Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
1990-2-12
pubmed:abstractText
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.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-1083489, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-13714851, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-13859478, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-14402240, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-16992124, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-2411932, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-2414434, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-2457698, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-2600845, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-3873536, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-4547276, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-4679725, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-512954, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-568176, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-6111797, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-6131450, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-6270629, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-6272286, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-6273573, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-6296368, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-6323703, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-6323704, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-6325785, http://linkedlifedata.com/resource/pubmed/commentcorrection/2607427-7381423
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0022-3751
pubmed:author
pubmed:issnType
Print
pubmed:volume
414
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
111-24
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1989
pubmed:articleTitle
Single inwardly rectifying potassium channels in cultured muscle cells from rat and mouse.
pubmed:affiliation
Department of Physiology, University of Leicester.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't