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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
45
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pubmed:dateCreated |
2007-11-7
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pubmed:abstractText |
Ca2+ channels play crucial roles in cellular signal transduction and are important targets of pharmacological agents. They are also associated with auxiliary subunits exhibiting functions that are still incompletely resolved. Skeletal muscle L-type Ca2+ channels (dihydropyridine receptors, DHPRs) are specialized for the remote voltage control of type 1 ryanodine receptors (RyR1) to release stored Ca2+. The skeletal muscle-specific gamma subunit of the DHPR (gamma 1) down-modulates availability by altering its steady state voltage dependence. The effect resembles the action of certain Ca2+ antagonistic drugs that are thought to stabilize inactivated states of the DHPR. In the present study we investigated the cross influence of gamma 1 and Ca2+ antagonists by using wild-type (gamma+/+) and gamma 1 knockout (gamma-/-) mice. We studied voltage-dependent gating of both L-type Ca2+ current and Ca2+ release and the allosteric modulation of drug binding. We found that 10 microM diltiazem, a benzothiazepine drug, more than compensated for the reduction in high-affinity binding of the dihydropyridine agent isradipine caused by gamma 1 elimination; 5 muM devapamil [(-)D888], a phenylalkylamine Ca2+ antagonist, approximately reversed the right-shifted voltage dependence of availability and the accelerated recovery kinetics of Ca2+ current and Ca2+ release. Moreover, the presence of gamma 1 altered the effect of D888 on availability and strongly enhanced its impact on recovery kinetics demonstrating that gamma 1 and the drug do not act independently of each other. We propose that the gamma 1 subunit of the DHPR functions as an endogenous Ca2+ antagonist whose task may be to minimize Ca2+ entry and Ca2+ release under stress-induced conditions favoring plasmalemma depolarization.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-10799530,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-11015618,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-11863426,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-12409298,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-12850214,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-1321525,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-1328292,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-14676283,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-15504904,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-15528246,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-16088377,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-1652439,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-17138559,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-2057528,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-2348396,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-2451721,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-2557440,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-300786,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-3023084,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-3418320,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-3487641,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-3496921,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-3498826,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-6309565,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-6604805,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-7742348,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-8245817,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-8913365,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-9065970,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-9131258,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-9132014,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-9545033,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17978188-9584627
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0027-8424
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
6
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pubmed:volume |
104
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
17885-90
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:17978188-Animals,
pubmed-meshheading:17978188-Calcium Channel Blockers,
pubmed-meshheading:17978188-Calcium Channels, L-Type,
pubmed-meshheading:17978188-Hindlimb,
pubmed-meshheading:17978188-Mice,
pubmed-meshheading:17978188-Mice, Knockout,
pubmed-meshheading:17978188-Muscle, Skeletal,
pubmed-meshheading:17978188-Muscle Fibers, Skeletal,
pubmed-meshheading:17978188-Patch-Clamp Techniques,
pubmed-meshheading:17978188-Protein Subunits
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pubmed:year |
2007
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pubmed:articleTitle |
The auxiliary subunit gamma 1 of the skeletal muscle L-type Ca2+ channel is an endogenous Ca2+ antagonist.
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pubmed:affiliation |
Institut für Angewandte Physiologie, Universität Ulm, Albert-Einstein-Allee 11, D-89069 Ulm, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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