Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:1775198rdf:typepubmed:Citationlld:pubmed
pubmed-article:1775198lifeskim:mentionsumls-concept:C0036945lld:lifeskim
pubmed-article:1775198lifeskim:mentionsumls-concept:C0018787lld:lifeskim
pubmed-article:1775198lifeskim:mentionsumls-concept:C0034144lld:lifeskim
pubmed-article:1775198lifeskim:mentionsumls-concept:C0032821lld:lifeskim
pubmed-article:1775198lifeskim:mentionsumls-concept:C0042523lld:lifeskim
pubmed-article:1775198lifeskim:mentionsumls-concept:C0021467lld:lifeskim
pubmed-article:1775198lifeskim:mentionsumls-concept:C0030163lld:lifeskim
pubmed-article:1775198lifeskim:mentionsumls-concept:C0021469lld:lifeskim
pubmed-article:1775198lifeskim:mentionsumls-concept:C0521116lld:lifeskim
pubmed-article:1775198lifeskim:mentionsumls-concept:C1527240lld:lifeskim
pubmed-article:1775198lifeskim:mentionsumls-concept:C0078728lld:lifeskim
pubmed-article:1775198pubmed:issue6lld:pubmed
pubmed-article:1775198pubmed:dateCreated1992-3-5lld:pubmed
pubmed-article:1775198pubmed:abstractTextThe electrophysiologic mode of action and potency of the verapamil derivative YS 035 (N,N-bis-(3,4-dimethoxyphenethyl)-N-methyl amine) were investigated in sheep cardiac Purkinje fibres. Action potential duration measured at a repolarization level of -60 mV (APD-60) and membrane currents recorded with the two-microelectrode voltage-clamp technique were evaluated. At 10 mumols/l YS 035 APD-60 was increased to about 115% of reference. Prolongation measured as percentage of the respective control exhibited on the average no dependence on stimulation frequency (0.17-2 Hz). At 100 mumols/l membrane became depolarized to about -50 mV and action potentials could no longer be elicited. Further study was focussed on effects on outward currents, mostly activated at a frequency of 0.05 Hz. Transient outward current (ito) was completely blocked at 100 mumols/l and half-maximal inhibition occurred at about 14 mumols/l. Inwardly rectifying potassium current (ik1) was reduced to 47% of reference at 100 mumols/l. An initially activating outward current at positive membrane potentials (iinst) was reduced to 73% at 100 mumols/l. Time-dependent (delayed) outward current (iK) was on the average not affected up to 100 mumols/l. Besides inhibition of repolarizing outward currents YS 035 completely blocked pacemaker current (if) at 100 mumols/l and half-maximal reduction was achieved at 5 mumols/l. YS 035 (1-100 mumols/l) did not clearly affect time constants of activation at selected test potentials (IK: +35 mV; if: -90 mV) or inactivation (ito: 0 mV). Voltage-dependent control mechanisms of currents (ito, if) were not influenced by YS 035 but the amount of available current was reduced.(ABSTRACT TRUNCATED AT 250 WORDS)lld:pubmed
pubmed-article:1775198pubmed:languageenglld:pubmed
pubmed-article:1775198pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1775198pubmed:citationSubsetIMlld:pubmed
pubmed-article:1775198pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1775198pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1775198pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1775198pubmed:statusMEDLINElld:pubmed
pubmed-article:1775198pubmed:monthDeclld:pubmed
pubmed-article:1775198pubmed:issn0028-1298lld:pubmed
pubmed-article:1775198pubmed:authorpubmed-author:BergerFFlld:pubmed
pubmed-article:1775198pubmed:authorpubmed-author:BorchardUUlld:pubmed
pubmed-article:1775198pubmed:authorpubmed-author:WeisTTlld:pubmed
pubmed-article:1775198pubmed:authorpubmed-author:HafnerDDlld:pubmed
pubmed-article:1775198pubmed:authorpubmed-author:KammerTTlld:pubmed
pubmed-article:1775198pubmed:issnTypePrintlld:pubmed
pubmed-article:1775198pubmed:volume344lld:pubmed
pubmed-article:1775198pubmed:ownerNLMlld:pubmed
pubmed-article:1775198pubmed:authorsCompleteYlld:pubmed
pubmed-article:1775198pubmed:pagination653-61lld:pubmed
pubmed-article:1775198pubmed:dateRevised2006-11-15lld:pubmed
pubmed-article:1775198pubmed:meshHeadingpubmed-meshheading:1775198-...lld:pubmed
pubmed-article:1775198pubmed:meshHeadingpubmed-meshheading:1775198-...lld:pubmed
pubmed-article:1775198pubmed:meshHeadingpubmed-meshheading:1775198-...lld:pubmed
pubmed-article:1775198pubmed:meshHeadingpubmed-meshheading:1775198-...lld:pubmed
pubmed-article:1775198pubmed:meshHeadingpubmed-meshheading:1775198-...lld:pubmed
pubmed-article:1775198pubmed:meshHeadingpubmed-meshheading:1775198-...lld:pubmed
pubmed-article:1775198pubmed:meshHeadingpubmed-meshheading:1775198-...lld:pubmed
pubmed-article:1775198pubmed:meshHeadingpubmed-meshheading:1775198-...lld:pubmed
pubmed-article:1775198pubmed:meshHeadingpubmed-meshheading:1775198-...lld:pubmed
pubmed-article:1775198pubmed:year1991lld:pubmed
pubmed-article:1775198pubmed:articleTitleInhibition of potassium outward currents and pacemaker current in sheep cardiac Purkinje fibres by the verapamil derivative YS 035.lld:pubmed
pubmed-article:1775198pubmed:affiliationInstitut für Pharmakologie, Universität Düsseldorf, Federal Republic of Germany.lld:pubmed
pubmed-article:1775198pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1775198pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed