|
|
Permissive role of reduced inwardly-rectifying potassium current density in the automaticity of the guinea pig pulmonary vein myocardium
|
|
|
|
|
نویسنده
|
tsuneoka y. ,irie m. ,tanaka y. ,sugimoto t. ,kobayashi y. ,kusakabe t. ,kato k. ,hamaguchi s. ,namekata i. ,tanaka h.
|
منبع
|
journal of pharmacological sciences - 2017 - دوره : 133 - شماره : 4 - صفحه:195 -202
|
چکیده
|
The electrophysiological properties underlying the automaticity of the guinea pig pulmonary vein myocardium were studied. about 30% of the isolated pulmonary vein tissue preparations showed spontaneous electrical activity,as shown by glass microelectrode recordings from their myocardial layer. the remaining quiescent preparations had a resting membrane potential less negative than that in the left atria. blockade of the acetylcholine activated potassium current (ik-ach) by tertiapin induced a depolarizing shift of the resting membrane potential and automatic electrical activity in the pulmonary vein,but not in the atria. the tertiapin-induced electrical activity,as well as the spontaneous activity,was inhibited by the application of carbachol or by chelation of intracellular ca2+ by bapta. the isolated pulmonary vein cardiomyocytes had an ik-ach density similar to that of the atrial cardiomyocytes,but a lower density of the inwardly-rectifying potassium current (ik1). spontaneous ca2+ transients were observed in about 30% of the isolated pulmonary vein cardiomyocytes,but not in atrial cardiomyocytes. the ca2+ transients in the pulmonary vein cardiomyocytes were induced by tertiapin and inhibited by carbachol. these results indicate that the pulmonary vein cardiomyocytes have a reduced density of the inwardly-rectifying potassium current,which plays a permissive role in their intracellular ca2+-dependent automaticity. © 2017 the authors
|
کلیدواژه
|
Automaticity; Intracellular Ca2+; Potassium channel; Pulmonary vein myocardium; Resting membrane potential
|
آدرس
|
department of pharmacology,faculty of pharmaceutical sciences,toho university,funabashi,chiba 274-8510,japan,laboratory of pharmacology,faculty of pharmaceutical science,tokyo university of sciences,noda,chiba 278-8510, Japan, department of pharmacology,faculty of pharmaceutical sciences,toho university,funabashi,chiba 274-8510, Japan, department of pharmacology,faculty of pharmaceutical sciences,toho university,funabashi,chiba 274-8510, Japan, department of pharmacology,faculty of pharmaceutical sciences,toho university,funabashi,chiba 274-8510, Japan, department of pharmacology,faculty of pharmaceutical sciences,toho university,funabashi,chiba 274-8510, Japan, department of organic chemistry,faculty of pharmaceutical sciences,toho university,funabashi,chiba 274-8510, Japan, department of organic chemistry,faculty of pharmaceutical sciences,toho university,funabashi,chiba 274-8510, Japan, department of pharmacology,faculty of pharmaceutical sciences,toho university,funabashi,chiba 274-8510, Japan, department of pharmacology,faculty of pharmaceutical sciences,toho university,funabashi,chiba 274-8510, Japan, department of pharmacology,faculty of pharmaceutical sciences,toho university,funabashi,chiba 274-8510, Japan
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Authors
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|