CALCITONIN-GENE-RELATED PEPTIDE ACTIVATES THE MUSCARINIC-GATED K+ CURRENT IN ATRIAL CELLS

被引:36
作者
KIM, DH
机构
[1] Department of Physiology and Biophysics, Chicago Medical School, North Chicago, 60064, IL
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 1991年 / 418卷 / 04期
关键词
CALCITONIN-GENE-RELATED PEPTIDE; MUSCARINIC RECEPTOR; K+ CHANNEL; ATRIAL CELLS; GTP-BINDING PROTEIN; ATP-SENSITIVE K+ CHANNEL;
D O I
10.1007/BF00550871
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
A high density of nerve fibers containing calcitonin-gene-related peptide (CGRP) is present in the atria. Recently CGRP was reported to open ATP-sensitive K+ channels in arterial smooth muscle cells. This study examines whether CGRP activates a similar K+ channel in cardiac cells. In voltage-clamped whole cells loaded with GTP and ATP, CGRP reversibly evoked an inwardly rectifying K+ current. To identify the K+ channel that gives rise to this current, three types of K+ channel (resting, ATP-sensitive and acetylcholine-activated) were examined. CGRP failed to activate or inhibit the ATP-sensitive or the resting K+ channel. However, CGRP (0.1-1-mu-M) caused activation of single channels with kinetics similar to that of the muscarinic K+ channel (35-40 pS conductance and approx. 1 ms mean open time in symmetrical 140 mM K+). In excised, inside-out (CGRP in pipette) or in outside-out (GTP in pipette) patches, the K+ current was activated by perfusion with GTP or CGRP, respectively, suggesting that CGRP activated the muscarinic K+ channel via GTP-binding protein. Treatment with pertussis toxin inhibited the activation of the K+ channel, suggesting that CGRP receptor may be coupled to a G(i) or a G(o) type of GTP-binding protein. Together with previous findings, these results suggest that CGRP modulates several types of ion channels to produce its cellular effects.
引用
收藏
页码:338 / 345
页数:8
相关论文
共 33 条
[1]   UNCOUPLING OF CARDIAC MUSCARINIC AND BETA-ADRENERGIC RECEPTORS FROM ION CHANNELS BY A GUANINE-NUCLEOTIDE ANALOG [J].
BREITWIESER, GE ;
SZABO, G .
NATURE, 1985, 317 (6037) :538-540
[2]   2 DISTINCT TYPES OF INWARDLY RECTIFYING K+ CHANNELS IN BULLFROG ATRIAL MYOCYTES [J].
CLARK, RB ;
NAKAJIMA, T ;
GILES, W ;
KANAI, K ;
MOMOSE, Y ;
SZABO, G .
JOURNAL OF PHYSIOLOGY-LONDON, 1990, 424 :229-251
[3]   MODULATION OF THE DELAYED RECTIFIER POTASSIUM CURRENT IN FROG CARDIOMYOCYTES BY BETA-ADRENERGIC AGONISTS AND MAGNESIUM [J].
DUCHATELLEGOURDON, I ;
HARTZELL, HC ;
LAGRUTTA, AA .
JOURNAL OF PHYSIOLOGY-LONDON, 1989, 415 :251-274
[4]   ALPHA-ADRENERGIC MODULATION OF THE TRANSIENT OUTWARD CURRENT IN RABBIT ATRIAL MYOCYTES [J].
FEDIDA, D ;
SHIMONI, Y ;
GILES, WR .
JOURNAL OF PHYSIOLOGY-LONDON, 1990, 423 :257-277
[5]   CALCITONIN GENE-RELATED PEPTIDE (CGRP) AND CAPSAICIN-INDUCED STIMULATION OF HEART CONTRACTILE RATE AND FORCE [J].
FRANCOCERECEDA, A ;
LUNDBERG, JM .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1985, 331 (2-3) :146-151
[6]   G-PROTEINS - TRANSDUCERS OF RECEPTOR-GENERATED SIGNALS [J].
GILMAN, AG .
ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 :615-649
[7]   IMPROVED PATCH-CLAMP TECHNIQUES FOR HIGH-RESOLUTION CURRENT RECORDING FROM CELLS AND CELL-FREE MEMBRANE PATCHES [J].
HAMILL, OP ;
MARTY, A ;
NEHER, E ;
SAKMANN, B ;
SIGWORTH, FJ .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1981, 391 (02) :85-100
[8]   IONIC BASIS OF THE DIFFERENT ACTION-POTENTIAL CONFIGURATIONS OF SINGLE GUINEA-PIG ATRIAL AND VENTRICULAR MYOCYTES [J].
HUME, JR ;
UEHARA, A .
JOURNAL OF PHYSIOLOGY-LONDON, 1985, 368 (NOV) :525-&
[9]   EFFECTS OF CALCITONIN GENE-RELATED PEPTIDE (CGRP) AND ISOPROTERENOL ON THE CONTRACTILITY AND ADENYLATE-CYCLASE ACTIVITY IN THE RAT-HEART [J].
ISHIKAWA, T ;
OKAMURA, N ;
SAITO, A ;
GOTO, K .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1987, 19 (08) :723-727
[10]   POSITIVE INOTROPIC EFFECT OF CALCITONIN GENE-RELATED PEPTIDE MEDIATED BY CYCLIC-AMP IN GUINEA-PIG HEART [J].
ISHIKAWA, T ;
OKAMURA, N ;
SAITO, A ;
MASAKI, T ;
GOTO, K .
CIRCULATION RESEARCH, 1988, 63 (04) :726-734