Modulation of the K+ channels encoded by the human ethera-gogo-related gene-1 (hERG1) by nitric oxide

Citation
M. Taglialatela et al., Modulation of the K+ channels encoded by the human ethera-gogo-related gene-1 (hERG1) by nitric oxide, MOLEC PHARM, 56(6), 1999, pp. 1298-1308
Citations number
44
Language
INGLESE
art.tipo
Article
Categorie Soggetti
Pharmacology & Toxicology
Journal title
MOLECULAR PHARMACOLOGY
ISSN journal
0026-895X → ACNP
Volume
56
Issue
6
Year of publication
1999
Pages
1298 - 1308
Database
ISI
SICI code
0026-895X(199912)56:6<1298:MOTKCE>2.0.ZU;2-M
Abstract
The inhibition of nitric oxide synthase by N-nitro-L-arginine methyl ester (0.03-3 mM) dose-dependently reduced nitric oxide (NO.) levels and enhanced the outward currents carried by human ether-a-gogo-related gene-1 (hERG1) K+ channels expressed in Xenopus laevis oocytes, whereas the increase in NO . levels achieved by exposure to L-arginine (0.03-10 mM) inhibited these cu rrents. Furthermore, four NO. donors belonging to such different chemical c lasses as sodium nitroprusside (1-1000 mu M), 3-morpholino-sydnonimine (100 -1000 mu M), (Z)-1-[N-(2-aminoethyl)-N-(2-ammonioethyl)amino]diazen-1-ium-1 ,2-diolate (NOC-18; 1-300 mu M), and S-nitroso N-acetylpenicillamine (1-300 mu M) dose-dependently inhibited hERG1 outward K+ currents. By contrast, t he NO. donor NOC-18 (0.3 mu M) did not affect other cloned K+ channels such as rat neuroblastoma-glioma K+ channel 2, rat delayed rectifier K+ channel 1, bovine ether-a-gogo gene, rat ether-a-gogo-related gene-2, and rat ethe r-a-gogo-related gene-3. The inhibitory effect of NO. donors on hERG1 K+ ch annels was prevented by the NO. scavengers 2-phenyl-4,4,5,5-tetramethylimid azoline-1-oxyl-3-oxide and hemoglobin. The membrane permeable analog of cGM P, 8-bromo-cGMP (1 mM), failed to reproduce the inhibitory action of NO. do nors on hERG1 outward currents; furthermore, the specific inhibitor of the NO.-dependent guanylyl cyclase, 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (50 mu M), neither interfered with outward hERG1 K+ currents nor prevented their inhibition by 0.3 mM NOC-18. Both L-arginine (10 mu M) and NOC-18 (0 .3 mM) counteracted the stimulatory effect on hERG1 outward currents induce d by the radical oxygen species-generating system FeSO4 (25 mu M)/ascorbic acid (50 mu M; Fe/Asc). Finally, L-arginine (10 mu M) and NOC-18 (0.3 mM) i nhibited both basal and Fe/Asc (0.1 mM/0.2 mM) stimulated lipid peroxidatio n in X. laevis oocytes. Collectively, the present results suggest that NO., both endogenously produced and pharmacologically delivered, may exert in a cGMP-independent way an inhibitory effect on hERG1 outward K+ currents via an interaction with radical oxygen species either generated under resting conditions or triggered by Fe/Asc.