CYCLIC GMP-MEDIATED INHIBITION OF L-TYPE CA2+ CHANNEL ACTIVITY BY HUMAN NATRIURETIC PEPTIDE IN RABBIT HEART-CELLS

被引:80
作者
TOHSE, N [1 ]
NAKAYA, H [1 ]
TAKEDA, Y [1 ]
KANNO, M [1 ]
机构
[1] HOKKAIDO UNIV,SCH MED,DEPT PHARMACOL,SAPPORO,HOKKAIDO 060,JAPAN
关键词
ATRIAL NATRIURETIC PEPTIDE; CYCLIC GMP; L-TYPE CA2+ CHANNEL; CARDIOMYOCYTE; PATCH CLAMP;
D O I
10.1111/j.1476-5381.1995.tb13316.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 Effects of atrial natriuretic peptide (ANP) on the L-type Ca2+ channels were examined in rabbit isolated ventricular cells by use of whole-cell and cell-attached configurations of the patch clamp methods. ANP produced a concentration-dependent decrease (10-100 nM) in amplitude of a basal Ca2+ channel current. 2 The inactive ANP (methionine-oxidized ANP, 30 nM) failed to decrease the current. 3 8-Bromo-cyclic GMP (300 mu M), a potent activator of cyclic GMP-dependent protein kinase (PKG), produced the same effects on the basal Ca2+ channel current as those produced by ANP. The cyclic GMP-induced inhibition of the Ca2+ channel current was still evoked in the presence of 1-isobutyl-3-methyl-xanthine, an inhibitor of phosphodiesterase. ANP failed to produce inhibition of the Ca2+ channel current in the presence of 8-bromo-cyclic GMP. 4 In the single channel recording, ANP and 8-bromo-cyclic GMP also inhibited the activities of the L-type Ca2+ channels. Both agents decreased the open probability (NP0) without affecting the unit amplitude. 5 The present results suggest that ANP inhibits the cardiac L-type Ca2+ channel activity through the intracellular production of cyclic GMP and then activation of PKG.
引用
收藏
页码:1076 / 1082
页数:7
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