A PHARMACOKINETIC ANALYSIS OF 3,4-METHYLENEDIOXYMETHAMPHETAMINE EFFECTS ON MONOAMINE CONCENTRATIONS IN BRAIN DIALYSATES

被引:8
作者
HIRAMATSU, M [1 ]
DISTEFANO, E [1 ]
CHANG, AS [1 ]
CHO, AK [1 ]
机构
[1] UNIV CALIF LOS ANGELES,CTR HLTH SCI,MED CTR,SCH MED,DEPT PHARMACOL,10833 LE CONTE AVE,LOS ANGELES,CA 90024
关键词
MDMA (3,4-METHYLENEDIOXYMETHAMPHETAMINE); DOPAMINE RELEASE; MICRODIALYSIS (INVIVO); ENANTIOMERS; PHARMACOKINETICS; PHARMACODYNAMICS;
D O I
10.1016/0014-2999(91)90697-O
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Interpretation of the in vivo actions of 3,4-methylenedioxymethamphetamine (MDMA) is complicated by the formation of the active metabolite, 3,4-methylenedioxyamphetamine (MDA). This study evaluates the role of MDA in the dopamine releasing actions of (+)-MDMA. In the study, rats were given subcutaneous doses of (+)-MDMA and concentrations of monoamines and their metabolites in striatal dialysate were measured at 15 min intervals. In parallel experiments, plasma concentrations of (+)- and (-)-MDMA and MDA were determined by GC/MS procedures. The time course of MDMA levels was comparable for the two isomers as were their bioavailabilities. In contrast, the plasma levels of MDA were about three times higher after (+)-MDMA. (+)-MDMA caused a rapid increase in striatal dialysate levels of dopamine and decreased extracellular levels of dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA). There was a significant correlation between dopamine concentration in striatal dialysate and plasma MDMA concentration, but not with plasma MDA. These results indicate that MDMA itself has stereoselective actions on dopamine neurons. However, the higher plasma MDA levels after (+)-MDMA may account for part of the enantiomeric differences in the behavioral and neurotoxicological effects of MDMA.
引用
收藏
页码:135 / 140
页数:6
相关论文
共 21 条
[1]  
ANDERSON WL, 1989, COMPUTER, V22, P8
[2]   PHARMACOLOGIC PROFILE OF MDMA (3,4-METHYLENEDIOXYMETHAMPHETAMINE) AT VARIOUS BRAIN RECOGNITION SITES [J].
BATTAGLIA, G ;
BROOKS, BP ;
KULSAKDINUN, C ;
DESOUZA, EB .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1988, 149 (1-2) :159-163
[3]  
BATTAGLIA G, 1987, J PHARMACOL EXP THER, V242, P911
[4]  
CHO AK, 1990, DRUG METAB DISPOS, V18, P686
[5]   STIMULUS PROPERTIES OF 1-(3,4-METHYLENEDIOXYPHENYL)-2-AMINOPROPANE (MDA) ANALOGS [J].
GLENNON, RA ;
YOUSIF, M ;
PATRICK, G .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1988, 29 (03) :443-449
[6]   THE EFFECT OF MDMA (ECSTASY) AND ITS OPTICAL ISOMERS ON SCHEDULE-CONTROLLED RESPONDING IN MICE [J].
GLENNON, RA ;
LITTLE, PJ ;
ROSECRANS, JA ;
YOUSIF, M .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1987, 26 (02) :425-426
[7]   THE EFFECT OF OPTICAL ISOMERS OF 3,4-METHYLENEDIOXYMETHAMPHETAMINE (MDMA) ON STEREOTYPED BEHAVIOR IN RATS [J].
HIRAMATSU, M ;
NABESHIMA, T ;
KAMEYAMA, T ;
MAEDA, Y ;
CHO, AK .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1989, 33 (02) :343-347
[8]   ENANTIOMERIC DIFFERENCES IN THE EFFECTS OF 3,4-METHYLENEDIOXYMETHAMPHETAMINE ON EXTRACELLULAR MONOAMINES AND METABOLITES IN THE STRIATUM OF FREELY-MOVING RATS - AN INVIVO MICRODIALYSIS STUDY [J].
HIRAMATSU, M ;
CHO, AK .
NEUROPHARMACOLOGY, 1990, 29 (03) :269-275
[9]  
JOHNSON M, 1988, J PHARMACOL EXP THER, V244, P977
[10]   EFFECTS OF THE ENANTIOMERS OF MDA, MDMA AND RELATED ANALOGS ON [H-3] SEROTONIN AND [H-3] DOPAMINE RELEASE FROM SUPERFUSED RAT-BRAIN SLICES [J].
JOHNSON, MP ;
HOFFMAN, AJ ;
NICHOLS, DE .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1986, 132 (2-3) :269-276