Effects of moderate alcohol consumption on the central nervous system

被引:486
作者
Eckardt, MJ
File, SE
Gessa, GL
Grant, KA
Guerri, C
Hoffman, PL
Kalant, H
Koob, GF
Li, TK
Tabakoff, B
机构
[1] Univ Colorado, Sch Med, Dept Pharmacol, Denver, CO 80262 USA
[2] NIAAA, Off Sci Affairs, Bethesda, MD 20205 USA
[3] Univ London, Guys Hosp, Psychopharmacol Res Unit, Div Pharmacol, London, England
[4] Univ Cagliari, Dipartimento Neurosci, Cagliari, Italy
[5] Wake Forest Univ, Bowman Gray Sch Med, Dept Physiol & Pharmacol, Winston Salem, NC 27103 USA
[6] Inst Invest Citological Caja Ahorros Valencia, Valencia, Spain
[7] Univ Colorado, Sch Med, Dept Pharmacol, Denver, CO 80202 USA
[8] Univ Toronto, Dept Pharmacol, Toronto, ON, Canada
[9] Scripps Res Inst, Dept Neuropharmacol, La Jolla, CA 92037 USA
[10] Indiana Univ, Sch Med, Indianapolis, IN 46202 USA
关键词
moderate; ethanol; brain; behavior; biology;
D O I
10.1111/j.1530-0277.1998.tb03695.x
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
The concept of moderate consumption of ethanol (beverage alcohol) has evolved over time from considering this level of intake to he nonintoxicating and noninjurious, to encompassing levels defined as "statistically" normal in particular populations, and the public health-driven concepts that define moderate drinking as the level corresponding to the lowest overall rate of morbidity or mortality in a population. The various approaches to defining moderate consumption of ethanol provide for a range of intakes that can result in blood ethanol concentrations ranging from 5 to 6 mg/dl, to levels of over 90 mg/dl (i.e., similar to 20 mM). This review summarizes available information regarding the effects of moderate consumption of ethanol on the adult and the developing nervous systems. The metabolism of ethanol in the human is reviewed to allow for proper appreciation of the important variables that interact to influence the level of exposure of the brain to ethanol once ethanol is orally consumed. At the neurochemical level, the moderate consumption of ethanol selectively affects the function of GABA, glutamatergic, serotonergic, dopaminergic, cholinergic, and opioid neuronal systems. Ethanol can affect these systems directly, and/or the interactions between and among these systems become important in the expression of ethanol's actions. The behavioral consequences of ethanol's actions on brain neurochemistry, and the neurochemical effects themselves, are very much dose- and time-related, and the collage of ethanol's actions can change significantly even on the rising and falling phases of the blood ethanol curve. The behavioral effects of moderate ethanol intake can encompass events that the human or other animal can perceive as reinforcing through either positive (e.g., pleasurable, activating) or negative (e.g., anxiolysis, stress reduction) reinforcement mechanisms. Genetic factors and gender play an important role in the metabolism and behavioral actions of ethanol, and doses of ethanol producing pleasurable feelings, activation, and reduction of anxiety in some humans/animals can have aversive, sedative, or no effect in others. Research on the cognitive effects of acute and chronic moderate intake of ethanol is reviewed, and although a number of studies have noted a measurable diminution in neuropsychologic parameters in habitual consumers of moderate amounts of ethanol, others have not found such changes. Recent studies have also noted some positive effects of moderate ethanol consumption on cognitive performance in the aging human. The moderate consumption of ethanol by pregnant women can have significant consequences on the developing nervous system of the fetus. Consumption of ethanol during pregnancy at levels considered to be in the moderate range can generate fetal alcohol effects (behavioral, cognitive anomalies) in the offspring. A number of factors-including gestational period, the periodicity of the mother's drinking, genetic factors, etc.-play important roles in determining the effect of ethanol on the developing central nervous system. A series of recommendations for future research endeavors, at all levels, is included with this review as part of the assessment of the effects of moderate ethanol consumption on the central nervous system.
引用
收藏
页码:998 / 1040
页数:43
相关论文
共 440 条
[1]   HON V STROH-BREWERY COMPANY - WHAT DO WE MEAN BY MODERATE AND HEAVY DRINKING [J].
ABEL, EL ;
KRUGER, ML .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1995, 19 (04) :1024-1031
[2]  
ABEL EL, 1984, FETAL ALCOHOL SYNDRO
[3]   BLOCKADE OF DELTA-OPIOID RECEPTORS IN THE NUCLEUS-ACCUMBENS PREVENTS ETHANOL-INDUCED STIMULATION OF DOPAMINE RELEASE [J].
ACQUAS, E ;
MELONI, M ;
DICHIARA, G .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1993, 230 (02) :239-241
[4]   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
[5]   MEMORY FACILITATION BY POST-TRAINING INJECTION OF ETHANOL [J].
ALKANA, RL ;
PARKER, ES .
PSYCHOPHARMACOLOGY, 1979, 66 (02) :117-119
[6]   ACUTE AND CHRONIC ETHANOL TREATMENTS ALTER GABA RECEPTOR-OPERATED CHLORIDE CHANNELS [J].
ALLAN, AM ;
HARRIS, RA .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1987, 27 (04) :665-670
[7]   EFFECTS OF SOCIAL DRINKING AND FAMILIAL ALCOHOLISM RISK ON COGNITIVE-FUNCTIONING - NULL FINDINGS [J].
ALTERMAN, AI ;
HALL, JG .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1989, 13 (06) :799-803
[8]   Disposition and first-pass metabolism of ethanol in humans: Is it gastric or hepatic and does it depend on gender? [J].
Ammon, E ;
Schafer, C ;
Hofmann, U ;
Klotz, U .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1996, 59 (05) :503-513
[9]   5-HT1A RECEPTORS IN THE MEDIAN RAPHE NUCLEUS AND DORSAL HIPPOCAMPUS MAY MEDIATE ANXIOLYTIC AND ANXIOGENIC BEHAVIORS RESPECTIVELY [J].
ANDREWS, N ;
HOGG, S ;
GONZALEZ, LE ;
FILE, SE .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1994, 264 (03) :259-264
[10]   SENSITIVITY OF N-METHYL-D-ASPARTATE (NMDA) AND NICOTINIC ACETYLCHOLINE-RECEPTORS TO ETHANOL AND PYRAZOLE [J].
ARACAVA, Y ;
FROESFERRAO, MM ;
PEREIRA, EFR ;
ALBUQUERQUE, EX .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1991, 625 :451-472