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dc.creatorHIDALGO,CECILIA
dc.creatorBULL,RICARDO
dc.creatorMARENGO,JUAN J
dc.creatorPÉREZ,CLAUDIO F
dc.creatorDONOSO,PAULINA
dc.date2000-01-01
dc.date.accessioned2019-05-02T21:20:58Z
dc.date.available2019-05-02T21:20:58Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0716-97602000000200011
dc.identifier.urihttp://revistaschilenas.uchile.cl/handle/2250/81327
dc.descriptionThe effects of redox reagents on the activity of the intracellular calcium release channels (ryanodine receptors) of skeletal and cardiac muscle, or brain cortex neurons, was examined. In lipid bilayer experiments, oxidizing agents (2,2'-dithiodipyridine or thimerosal) modified the calcium dependence of all single channels studied. After controlled oxidation channels became active at sub µM calcium concentrations and were not inhibited by increasing the calcium concentration to 0.5 mM. Subsequent reduction reversed these effects. Channels purified from amphibian skeletal muscle exhibited the same behavior, indicating that the SH groups responsible for modifying the calcium dependence belong to the channel protein. Parallel experiments that measured calcium release through these channels in sarcoplasmic reticulum vesicles showed that following oxidation, the channels were no longer inhibited by sub mM concentrations of Mg2+. It is proposed that channel redox state controls the high affinity sites responsible for calcium activation as well as the low affinity sites involved in Mg2+ inhibition of channel activity. The possible physiological and pathological implications of these results are discussed
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dc.languageen
dc.publisherSociedad de Biología de Chile
dc.relation10.4067/S0716-97602000000200011
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceBiological Research v.33 n.2 2000
dc.subjectcalcium dependence
dc.subjectneurons
dc.subjectredox state
dc.subjectryanodine receptors
dc.subjectsarcoplasmic reticulum
dc.subjectskeletal and cardiac muscle
dc.titleSH Oxidation Stimulates Calcium Release Channels (Ryanodine Receptors) From Excitable Cells


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