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[Intracellular Molecular Mechanisms of Adrenergic Regulation of Pulmonary Vein Myocardium Membrane Potential].
Rozenshtraukh, L V; Karimova, V M; Kuzmin, V S.
Afiliación
  • Rozenshtraukh LV; Institute of Cardiology of Russian Cardiology Scientific and Production Complex.
  • Karimova VM; Federal State Budgetary Educational Institution of Higher Education, "M. V. Lomonosov Moscow State University".
  • Kuzmin VS; Federal State Budgetary Educational Institution of Higher Education, "M. V. Lomonosov Moscow State University".
Kardiologiia ; 57(11): 34-41, 2017 Nov.
Article en Ru | MEDLINE | ID: mdl-29276916
Pulmonary vein (PV) myocardium is characterized by numerous electrophysiological properties which make this tissue highly prone to spontaneous, ectopic activity partially due to resting potential (RP) instability. PV derived ectopy frequently underlies supraventricular arrhythmias, including atrial fibrillation. It has also been demonstrated that adrenergic stimulation causes proarrhythmic alterations in PV. Selective α1- and ß-adrenoreceptors stimulation causes RP depolarization and hyperpolarization, respectively, at least in rats. The intracellular mechanisms of α1- and ß-adrenoreceptors-dependent RP drifts are not investigated. Adenylate cyclase (AC) activator forscolin similarly to selective ß-adrenoreceptors agonist isoproterenol (ISO) induced strong hyperpolarization in quiescent isolated perfused multicellular preparations of rat PV. Maximal value of hyperpolarization in PV was equal after application of both compounds. Proteinkinase A (PKA) inhibitors КТ5720, H-89 and Rp-adenosine-cAMP suppressed ISO-induced hyperpolarization in PV. Inhibitors of phospholipase C (U73122) or D (FIPI), similarly to proteinkinase C (PKC) inhibitor chelerythrine, failed to suppress α-adrenoreceptors-dependent phenylephrine-induced depolarization in rat PV myocardium. These results allow us to suggest that ß-adrenoreceptors-dependent RP hyperpolarization in quiescent rat PV myocardium is only partially mediated by cAMP-dependent signal transduction pathway and by PKA. Besides, PKA-independent mechanisms also contribute to ß-agonists effects in PV. In addition, α-adrenoreceptors-dependent depolarization in rat PV myocardium could be independent on PLC and PKC.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Venas Pulmonares Límite: Animals Idioma: Ru Revista: Kardiologiia Año: 2017 Tipo del documento: Article Pais de publicación: Rusia
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Venas Pulmonares Límite: Animals Idioma: Ru Revista: Kardiologiia Año: 2017 Tipo del documento: Article Pais de publicación: Rusia