A review of the validity and variability of the elevated plus-maze as an animal model of anxiety

被引:901
作者
Hogg, S [1 ]
机构
[1] UNITED MED & DENT SCH, GUYS HOSP,SCH MED,DIV PHARMACOL, PSYCHOPHARMACOL RES UNIT, LONDON SE1 9RT, ENGLAND
关键词
animal models; strain differences; handling; stress anxiolytics; anxiogenics;
D O I
10.1016/0091-3057(95)02126-4
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Despite or possibly by virtue of the fact that it is one of the most commonly used animal models of anxiety the Elevated Plus-Maze (EPM) results in a wide range of, often contradictory, results following pharmacological experiments. The responses from a questionnaire distributed to 65 groups that have published studies using the EPM in the past 3 years has, along with reference to published reports, enabled some conclusions regarding the influencing factors to be drawn. Some evidence for differential sensitivities between strains exists, with albino rats being more sensitive to the anxiolytic effects of 5-HT3 receptor antagonists and 5-HT1A receptor agonists than pigmented animals. Most important, however, is the manipulation of the animals prior to testing and the aversiveness of the test conditions themselves. Stressing animals before testing (e.g., by moving from holding to test room) or using more aversive test conditions (e.g., elevated light levels) increases sensitivity to potential anxiolytics. Animals that are habituated to gentle handling or tested in less aversive conditions (e.g., EPM with ledges) show reduced likelihood of anxiolytic responses with administration of 5-HT3 antagonists, 5-HT1A agonists, and benzodiazepines.
引用
收藏
页码:21 / 30
页数:10
相关论文
共 56 条
[1]  
ADAMEC R E, 1991, Journal of Psychopharmacology, V5, P175, DOI 10.1177/026988119100500301
[2]   LASTING EFFECTS ON RODENT ANXIETY OF A SINGLE EXPOSURE TO A CAT [J].
ADAMEC, RE ;
SHALLOW, T .
PHYSIOLOGY & BEHAVIOR, 1993, 54 (01) :101-109
[3]   BEHAVIORAL-RESPONSES TO SINGLE AND REPEATED RESTRAINT IN MALE AND FEMALE RATS [J].
ALBONETTI, ME ;
FARABOLLINI, F .
BEHAVIOURAL PROCESSES, 1992, 28 (1-2) :97-110
[4]   HANDLING HISTORY OF RATS MODIFIES BEHAVIORAL-EFFECTS OF DRUGS IN THE ELEVATED PLUS-MAZE TEST OF ANXIETY [J].
ANDREWS, N ;
FILE, SE .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1993, 235 (01) :109-112
[5]  
ANDREWS NA, 1991, BRIT J PHARMACOL, V120, pP305
[6]  
BALDWIN HA, 1986, PSYCHOPHARMACOLOGY, V89, pS9
[7]   THE INFLUENCE OF DIAZEPAM ON LEARNING-PROCESSES IMPAIRED BY PENTYLENETETRAZOL KINDLING [J].
BECKER, A ;
GRECKSCH, G ;
MATTHIES, H .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1994, 349 (05) :492-496
[8]   THE INFLUENCE OF 5-HYDROXYTRYPTAMINE REUPTAKE BLOCKADE ON CCK RECEPTOR ANTAGONIST EFFECTS IN THE RAT ELEVATED ZERO-MAZE [J].
BICKERDIKE, MJ ;
MARSDEN, CA ;
DOURISH, CT ;
FLETCHER, A .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1994, 271 (2-3) :403-411
[9]   GABAERGIC AND DOPAMINERGIC TRANSMISSION IN THE RAT CEREBRAL-CORTEX - EFFECT OF STRESS, ANXIOLYTIC AND ANXIOGENIC DRUGS [J].
BIGGIO, G ;
CONCAS, A ;
CORDA, MG ;
GIORGI, O ;
SANNA, E ;
SERRA, M .
PHARMACOLOGY & THERAPEUTICS, 1990, 48 (02) :121-142
[10]   CHRONIC HANDLING MODIFIES THE ANXIOLYTIC EFFECT OF DIAZEPAM IN THE ELEVATED PLUS-MAZE [J].
BRETT, RR ;
PRATT, JA .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1990, 178 (01) :135-138