FACILITATION OF 5-HYDROXYTRYPTAMINE(3) RECEPTOR DESENSITIZATION BY FLUOXETINE

被引:17
作者
FAN, P
机构
[1] Laboratory of Molecular and Cellular Neurobiology, National Institute on Alcohol Abuse and Alcoholism, Rockville, MD 20852
关键词
D O I
10.1016/0306-4522(94)90384-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Effect of fluoxetine on the desensitization of the inward current mediated by 5-hydroxytryptamine(3) receptors in rat nodose ganglion neurons was investigated with whole cell patch-clamp recording. 5-Hydroxytryptamine(3) current desensitization was best fitted in most experiments by a single exponential function and showed little dependence on membrane potential. Fluoxetine greatly facilitated the rate of 5-hydroxytryptamine, current desensitization in a dose-dependent manner. The effect of fluoxetine was gradual, long-lasting, voltage-independent and the recovery was incomplete. The IC50 value for the decrease of the desensitization time-constant by fluoxetine was 0.171 mu M and the Hill coefficient was 1.1. Fluoxetine also inhibited the peak and steady-state 5-hydroxytryptamine, current with the latter being more sensitive to fluoxetine. The IC50 value for the effect of fluoxetine on peak current was 1.27 mu M and that on steady-state current was 0.172 mu M. There is a highly significant correlation between the two effects of fluoxetine on current desensitization and on current amplitudes: r-values for the correlation between the decrease in time-constant and the reduction in peak and steady-state current amplitudes were 0.82 and 0.88, respectively (P < 0.001). This action of fluoxetine on 5-hydroxytryptamine, receptors may be involved in the behavioral effects of fluoxetine.
引用
收藏
页码:515 / 522
页数:8
相关论文
共 40 条
[1]   FLUOXETINE KINETICS AND PROTEIN-BINDING IN NORMAL AND IMPAIRED RENAL-FUNCTION [J].
ARONOFF, GR ;
BERGSTROM, RF ;
POTTRATZ, ST ;
SLOAN, RS ;
WOLEN, RL ;
LEMBERGER, L .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1984, 36 (01) :138-144
[2]   FLUOXETINE - A REVIEW OF RECEPTOR AND FUNCTIONAL-EFFECTS AND THEIR CLINICAL IMPLICATIONS [J].
BEASLEY, CM ;
MASICA, DN ;
POTVIN, JH .
PSYCHOPHARMACOLOGY, 1992, 107 (01) :1-10
[3]   5-HT - ON THE PSYCHIATRISTS COUCH [J].
BRILEY, M ;
GRAHAMESMITH, D .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1992, 13 (09) :337-338
[4]   ANXIOLYTIC POTENTIAL OF 5-HT3 RECEPTOR ANTAGONISTS [J].
COSTALL, B ;
NAYLOR, RJ .
PHARMACOLOGY & TOXICOLOGY, 1992, 70 (03) :157-162
[5]   THE PSYCHOPHARMACOLOGY OF 5-HT3 RECEPTORS [J].
COSTALL, B ;
NAYLOR, RJ ;
TYERS, MB .
PHARMACOLOGY & THERAPEUTICS, 1990, 47 (02) :181-202
[6]   SIMULTANEOUS ANALYSIS OF FAMILIES OF SIGMOIDAL CURVES - APPLICATION TO BIOASSAY, RADIOLIGAND ASSAY, AND PHYSIOLOGICAL DOSE-RESPONSE CURVES [J].
DELEAN, A ;
MUNSON, PJ ;
RODBARD, D .
AMERICAN JOURNAL OF PHYSIOLOGY, 1978, 235 (02) :E97-E102
[7]   5-HT3 RECEPTORS ARE MEMBRANE ION CHANNELS [J].
DERKACH, V ;
SURPRENANT, A ;
NORTH, RA .
NATURE, 1989, 339 (6227) :706-709
[8]  
Fan P., 1992, Society for Neuroscience Abstracts, V18, P800
[9]  
FOZARD JR, 1992, INT ACAD B, V1, P44
[10]   FLUOXETINE, A SELECTIVE INHIBITOR OF SEROTONIN UPTAKE [J].
FULLER, RW ;
WONG, DT ;
ROBERTSON, DW .
MEDICINAL RESEARCH REVIEWS, 1991, 11 (01) :17-34