Your browser doesn't support javascript.
loading
K2p 3.1 protein is expressed as a transmural gradient across the rat left ventricular free wall.
Jones, Sandra A; Walton, Richard D; Morton, Michael; Lancaster, Matthew K.
Afiliação
  • Jones SA; Department of Biomedical Sciences, Department Faculty of Health Sciences, University of Hull, Hull, UK.
  • Walton RD; Centre de Recherche Cardio-Thoracique de Bordeaux U1045, Université de Bordeaux, Bordeaux, France.
  • Morton M; Inserm, Centre de Recherche Cardio-Thoracique de Bordeaux, Bordeaux, France.
  • Lancaster MK; L'Institut de Rythmologie et Modélisation Cardiaque LIRYC, Fondation Bordeaux Université, Bordeaux, France.
J Cardiovasc Electrophysiol ; 30(3): 383-391, 2019 03.
Article em En | MEDLINE | ID: mdl-30516300
INTRODUCTION: K2p 3.1, also known as TASK-1, is a twin-pore acid-sensitive repolarizing K+ channel, responsible for a background potassium current that significantly contributes to setting the resting membrane potential of cardiac myocytes. Inhibition of IK2p3.1 alters cardiac repolarization and is proarrhythmogenic. In this study, we have examined the expression of K2p 3.1 and function of this channel in tissue and myocytes from across the left ventricular free wall. METHODS AND RESULTS: Using fluorescence immunocytochemistry, the expression of K2p 3.1 protein in myocytes from the subendocardial region was found to be twice (205% ± 13.5%) that found in myocytes from the subepicardial region of the left ventricle (100% ± 5.3%). The left ventricular free wall exhibited a marked transmural gradient of K2p 3.1 protein expression. Western blot analysis confirmed significantly higher K2p 3.1 protein expression in subendocardial tissue (156% ± 2.5%) than subepicardial tissue (100% ± 5.0%). However, there was no difference in K2p 3.1 messenger RNA expression. Whole-cell patch clamp identified IK2p3.1 current density to be significantly greater in myocytes isolated from the subendocardium (7.66 ± 0.53 pA/pF) compared with those from the subepicardium (3.47 ± 0.74 pA/pF). CONCLUSIONS: This is the first study to identify a transmural gradient of K2p 3.1 in the left ventricle. This gradient has implications for understanding ventricular arrhythmogenesis under conditions of ischemia but also in response to other modulatory factors, such as adrenergic stimulation and the presence of anesthetics that inhibits or activates this channel.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Canais de Potássio de Domínios Poros em Tandem / Miócitos Cardíacos / Ventrículos do Coração / Proteínas do Tecido Nervoso Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Cardiovasc Electrophysiol Assunto da revista: ANGIOLOGIA / CARDIOLOGIA / FISIOLOGIA Ano de publicação: 2019 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Canais de Potássio de Domínios Poros em Tandem / Miócitos Cardíacos / Ventrículos do Coração / Proteínas do Tecido Nervoso Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Cardiovasc Electrophysiol Assunto da revista: ANGIOLOGIA / CARDIOLOGIA / FISIOLOGIA Ano de publicação: 2019 Tipo de documento: Article País de publicação: Estados Unidos