Matches in SemOpenAlex for { <https://semopenalex.org/work/W4385649102> ?p ?o ?g. }
- W4385649102 endingPage "111595" @default.
- W4385649102 startingPage "111595" @default.
- W4385649102 abstract "A common side effect of pharmaceutical drugs is an increased propensity for cardiac arrhythmias. Many drugs bind to cardiac ion-channels in a state-specific manner, which alters the ionic conductances in complicated ways, making it difficult to identify the mechanisms underlying pro-arrhythmic drug effects. To better understand the fundamental mechanisms underlying the diverse effects of state-dependent sodium (Na+) channel blockers on cellular excitability, we consider two canonical motifs of drug-ion-channel interactions and compare the effects of Na+ channel blockers on the rate-dependence of peak upstroke velocity, conduction velocity, and vulnerable window size. In the literature, both motifs are referred to as guarded receptor, but here we distinguish between state-specific binding that does not alter channel gating (referred to here as guarded receptor) and state-specific binding that blocks certain gating transitions (gate immobilization). For each drug binding motif, we consider drugs that bind to the inactivated state and drugs that bind to the non-inactivated state of the Na+ channel. Exploiting the idealized nature of the canonical binding motifs, we identify the fundamental mechanisms underlying the effects on excitability of the various binding interactions. Specifically, we derive the voltage-dependence of the drug binding time constants and the equilibrium fractions of channels bound to drug, and we then derive a formula that incorporates these time constants and equilibrium fractions to elucidate the fundamental mechanisms. In the case of charged drug, we find that drugs that bind to inactivated channels exhibit greater rate-dependence than drugs that bind to non-inactivated channels. For neutral drugs, the effects of guarded receptor interactions are rate-independent, and we describe a novel mechanism for reverse rate-dependence resulting from neutral drug binding to non-inactivated channels via the gate immobilization motif." @default.
- W4385649102 created "2023-08-09" @default.
- W4385649102 creator A5011696578 @default.
- W4385649102 creator A5031553126 @default.
- W4385649102 creator A5082049761 @default.
- W4385649102 date "2023-09-01" @default.
- W4385649102 modified "2023-10-14" @default.
- W4385649102 title "Rate-dependent effects of state-specific sodium channel blockers in cardiac tissue: Insights from idealized models" @default.
- W4385649102 cites W1500785579 @default.
- W4385649102 cites W1571909560 @default.
- W4385649102 cites W1979671751 @default.
- W4385649102 cites W1985940938 @default.
- W4385649102 cites W1991781357 @default.
- W4385649102 cites W1996969350 @default.
- W4385649102 cites W2002374666 @default.
- W4385649102 cites W2004273976 @default.
- W4385649102 cites W2005182745 @default.
- W4385649102 cites W2014953544 @default.
- W4385649102 cites W2028600729 @default.
- W4385649102 cites W2069884282 @default.
- W4385649102 cites W2072195498 @default.
- W4385649102 cites W2072951700 @default.
- W4385649102 cites W2074705578 @default.
- W4385649102 cites W2077936658 @default.
- W4385649102 cites W2082311140 @default.
- W4385649102 cites W2088624984 @default.
- W4385649102 cites W2093638125 @default.
- W4385649102 cites W2096511095 @default.
- W4385649102 cites W2107259824 @default.
- W4385649102 cites W2113420824 @default.
- W4385649102 cites W2115052737 @default.
- W4385649102 cites W2116411564 @default.
- W4385649102 cites W2126997063 @default.
- W4385649102 cites W2131262685 @default.
- W4385649102 cites W2139219494 @default.
- W4385649102 cites W2143518969 @default.
- W4385649102 cites W2151057609 @default.
- W4385649102 cites W2155932859 @default.
- W4385649102 cites W2156539232 @default.
- W4385649102 cites W2166297399 @default.
- W4385649102 cites W2184380802 @default.
- W4385649102 cites W2219910214 @default.
- W4385649102 cites W2606827815 @default.
- W4385649102 cites W2612743911 @default.
- W4385649102 cites W2892996644 @default.
- W4385649102 cites W3009375540 @default.
- W4385649102 cites W3127893500 @default.
- W4385649102 cites W3165275639 @default.
- W4385649102 cites W4210820117 @default.
- W4385649102 cites W4240181500 @default.
- W4385649102 cites W4301890533 @default.
- W4385649102 doi "https://doi.org/10.1016/j.jtbi.2023.111595" @default.
- W4385649102 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/37562674" @default.
- W4385649102 hasPublicationYear "2023" @default.
- W4385649102 type Work @default.
- W4385649102 citedByCount "0" @default.
- W4385649102 crossrefType "journal-article" @default.
- W4385649102 hasAuthorship W4385649102A5011696578 @default.
- W4385649102 hasAuthorship W4385649102A5031553126 @default.
- W4385649102 hasAuthorship W4385649102A5082049761 @default.
- W4385649102 hasBestOaLocation W43856491021 @default.
- W4385649102 hasConcept C107824862 @default.
- W4385649102 hasConcept C12554922 @default.
- W4385649102 hasConcept C170493617 @default.
- W4385649102 hasConcept C178790620 @default.
- W4385649102 hasConcept C185592680 @default.
- W4385649102 hasConcept C194544171 @default.
- W4385649102 hasConcept C2780035454 @default.
- W4385649102 hasConcept C50254741 @default.
- W4385649102 hasConcept C50952357 @default.
- W4385649102 hasConcept C537181965 @default.
- W4385649102 hasConcept C55493867 @default.
- W4385649102 hasConcept C86803240 @default.
- W4385649102 hasConcept C98274493 @default.
- W4385649102 hasConceptScore W4385649102C107824862 @default.
- W4385649102 hasConceptScore W4385649102C12554922 @default.
- W4385649102 hasConceptScore W4385649102C170493617 @default.
- W4385649102 hasConceptScore W4385649102C178790620 @default.
- W4385649102 hasConceptScore W4385649102C185592680 @default.
- W4385649102 hasConceptScore W4385649102C194544171 @default.
- W4385649102 hasConceptScore W4385649102C2780035454 @default.
- W4385649102 hasConceptScore W4385649102C50254741 @default.
- W4385649102 hasConceptScore W4385649102C50952357 @default.
- W4385649102 hasConceptScore W4385649102C537181965 @default.
- W4385649102 hasConceptScore W4385649102C55493867 @default.
- W4385649102 hasConceptScore W4385649102C86803240 @default.
- W4385649102 hasConceptScore W4385649102C98274493 @default.
- W4385649102 hasLocation W43856491021 @default.
- W4385649102 hasLocation W43856491022 @default.
- W4385649102 hasOpenAccess W4385649102 @default.
- W4385649102 hasPrimaryLocation W43856491021 @default.
- W4385649102 hasRelatedWork W1991585727 @default.
- W4385649102 hasRelatedWork W2031449089 @default.
- W4385649102 hasRelatedWork W2067421539 @default.
- W4385649102 hasRelatedWork W2082124037 @default.
- W4385649102 hasRelatedWork W2112596406 @default.
- W4385649102 hasRelatedWork W2232251872 @default.
- W4385649102 hasRelatedWork W2367894028 @default.