ALCOHOLS POTENTIATE ION CURRENT MEDIATED BY RECOMBINANT 5-HT(3)RA RECEPTORS EXPRESSED IN A MAMMALIAN-CELL LINE

被引:66
作者
LOVINGER, DM
ZHOU, Q
机构
[1] Department of Molecular Physiology and Biophysics, Vanderbilt University Medical School, Nashville, TN 37232-0615
关键词
SEROTONIN; ETHANOL; LIGAND-GATED CHANNELS; INTOXICATION; HUMAN EMBRYONIC KIDNEY CELLS; CATION CHANNELS; 5-HT; RECEPTOR;
D O I
10.1016/0028-3908(94)90131-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The effect of acute exposure to alcohols on ion current mediated by recombinant 5-HT(3)RA receptors transiently expressed in human embryonic kidney 293 cells was investigated. Cells transfected with 5-HT(3)RA cDNA expressed receptors with pharmacological and functional properties similar to those of native 5-HT, receptors. Potentiation of receptor-mediated cation current was observed in the presence of ethanol (10-100 mM), butanol (0.1-20 mM), isopentanol (0.01-25 mM) and trichloroethanol (0.5-25 mM). Potentiation increased in a concentration-dependent manner until saturation was achieved for all alcohols tested. The maximal efficacies of potentiation differed among the alcohols with isopentanol > butanol = trichloroethanol > ethanol. Potentiation by butanol and isopentanol appeared to show acute tolerance such that the percent increase in current amplitude was largest upon the first of a series of alcohol applications and decreased during subsequent applications. The effect of ethanol was variable with potentiation occurring in 74% of cells examined, but not in the remaining cells. These observations indicate that the potentiating action of alcohols is similar in recombinant receptors to that previously observed in neuroblastoma cells and neurons expressing native receptors. These findings indicate that this recombinant system is suitable for studying the molecular basis of alcohol actions on the 5-HT3 receptor.
引用
收藏
页码:1567 / 1572
页数:6
相关论文
共 31 条
[1]   ETHANOL POTENTIATES THE GABA-A-ACTIVATED CL- CURRENT IN MOUSE HIPPOCAMPAL AND CORTICAL-NEURONS [J].
AGUAYO, LG .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1990, 187 (01) :127-130
[2]   5-HT3 RECEPTORS ARE MEMBRANE ION CHANNELS [J].
DERKACH, V ;
SURPRENANT, A ;
NORTH, RA .
NATURE, 1989, 339 (6227) :706-709
[3]   MECHANISM OF INHIBITION OF N-METHYL-D-ASPARTATE-STIMULATED INCREASES IN FREE INTRACELLULAR CA2+ CONCENTRATION BY ETHANOL [J].
DILDYMAYFIELD, JE ;
LESLIE, SW .
JOURNAL OF NEUROCHEMISTRY, 1991, 56 (05) :1536-1543
[4]   ACTIONS OF VOLATILE ANESTHETICS AND ALCOHOLS ON CHOLINERGIC RECEPTOR CHANNELS [J].
DILGER, JP ;
BRETT, RS .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1991, 625 :616-627
[5]   MDL 72222, A SELECTIVE 5-HT3 RECEPTOR ANTAGONIST, SUPPRESSES VOLUNTARY ETHANOL-CONSUMPTION IN ALCOHOL-PREFERRING RATS [J].
FADDA, F ;
GARAU, B ;
MARCHEI, F ;
COLOMBO, G ;
GESSA, GL .
ALCOHOL AND ALCOHOLISM, 1991, 26 (02) :107-110
[6]   EFFECTS OF SOME ALIPHATIC-ALCOHOLS ON CONDUCTANCE CHANGE CAUSED BY A QUANTUM OF ACETYLCHOLINE AT TOAD ENDPLATE [J].
GAGE, PW ;
MCBURNEY, RN ;
SCHNEIDER, GT .
JOURNAL OF PHYSIOLOGY-LONDON, 1975, 244 (02) :409-429
[7]   BLOCKADE OF THE DISCRIMINATIVE STIMULUS EFFECTS OF ETHANOL WITH 5-HT3-RECEPTOR ANTAGONISTS [J].
GRANT, KA ;
BARRETT, JE .
PSYCHOPHARMACOLOGY, 1991, 104 (04) :451-456
[8]   N-METHYL-D-ASPARTATE RECEPTORS AND ETHANOL - INHIBITION OF CALCIUM FLUX AND CYCLIC-GMP PRODUCTION [J].
HOFFMAN, PL ;
RABE, CS ;
MOSES, F ;
TABAKOFF, B .
JOURNAL OF NEUROCHEMISTRY, 1989, 52 (06) :1937-1940
[9]   THE PROPERTIES OF 5-HT3 RECEPTORS IN CLONAL CELL-LINES STUDIED BY PATCH-CLAMP TECHNIQUES [J].
LAMBERT, JJ ;
PETERS, JA ;
HALES, TG ;
DEMPSTER, J .
BRITISH JOURNAL OF PHARMACOLOGY, 1989, 97 (01) :27-40
[10]   ETHANOL POTENTIATES AND BLOCKS NMDA-ACTIVATED SINGLE-CHANNEL CURRENTS IN RAT HIPPOCAMPAL PYRAMIDAL CELLS [J].
LIMALANDMAN, MTR ;
ALBUQUERQUE, EX .
FEBS LETTERS, 1989, 247 (01) :61-67