Environmental changes modify the expression of Diazepam withdrawal

被引:18
作者
Pérez, MF
Maglio, LE
Marchesini, GR
Molina, JC
Ramírez, OA [1 ]
机构
[1] Univ Nacl Cordoba, Fac Ciencias Quim, Dept Farmacol, RA-5000 Cordoba, Argentina
[2] Inst Invest Med M&M Ferreyra, Cordoba, Argentina
关键词
hippocampus; synaptic plasticity; long-term potentiation; conditioned abstinence; diazepam dependence; diazepam withdrawal;
D O I
10.1016/S0166-4328(02)00108-0
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
Early results from our laboratory have demonstrated a positive correlation between increased hippocampal synaptic plasticity and development of tolerance to hypolocomotive effect of Diazepam (DZ). We have found recently, that pre-exposure to DZ administration context impairs increase of hippocampal synaptic plasticity in conjunction with tolerance to DZ. These findings have suggested, that the tolerance to DZ is context specific. Furthermore, the hippocampus can be critically involved in the behavioral expression of conditioned tolerance to DZ. The results of the present investigation show that animals chronically treated with DZ for 18 days exhibit withdrawal signs, evaluated as an increased anxiety in an elevated plus maze. These animals also show, a facilitation in the threshold to induce long-term potentiation in the hippocampal formation. These phenomena have a strong dependency on the drug administration context, since both are reversed after the introduction of some changes in the drug administration environment. Furthermore, the alteration of some environmental cues increased the locomotive activity in animals that did not show anxiety as a withdrawal signs. We conclude that a common neural system could underlie the behavioral expression of the conditioned tolerance and dependence on DZ. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:75 / 81
页数:7
相关论文
共 30 条
[1]   ETHOPHARMACOLOGICAL ANALYSIS OF RAT BEHAVIOR ON THE ELEVATED PLUS-MAZE [J].
CRUZ, APM ;
FREI, F ;
GRAEFF, FG .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1994, 49 (01) :171-176
[2]   Effect of repeated ethanol withdrawal on glutamate microdialysate in the hippocampus [J].
Dahchour, A ;
De Witte, P .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1999, 23 (10) :1698-1703
[3]   DIZOCILPINE PREVENTS THE DEVELOPMENT OF TOLERANCE TO THE SEDATIVE EFFECTS OF DIAZEPAM IN RATS [J].
FILE, SE ;
FERNANDES, C .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1994, 47 (04) :823-826
[4]  
GRABOWSKI J, 1981, ADV SUBSTANCE ABUSE, V2
[5]  
KALANT H, 1973, ALCOHOL INTOXICATION, P3
[6]  
KALANT H, 1971, PHARMACOL REV, V23, P1047
[7]   DIFFERENTIAL INHIBITION BY NMDA ANTAGONISTS OF RAPID TOLERANCE TO, AND CROSS-TOLERANCE BETWEEN, ETHANOL AND CHLORDIAZEPOXIDE [J].
KHANNA, JM ;
MIHIC, SJ ;
WEINER, J ;
SHAH, G ;
WU, PH ;
KALANT, H .
BRAIN RESEARCH, 1992, 574 (1-2) :251-256
[8]  
Kippin TE, 1998, BEHAV NEUROSCI, V112, P1526
[9]   ANALYSIS OF 70 YEARS OF MORPHINE CLASSICAL-CONDITIONING - IMPLICATIONS FOR CLINICAL TREATMENT OF NARCOTIC ADDITION [J].
LYNCH, JJ ;
STEIN, EA ;
FERTZIGER, AP .
JOURNAL OF NERVOUS AND MENTAL DISEASE, 1976, 163 (01) :47-58
[10]   Preexposure to drug administration context blocks the development of tolerance to sedative effects of diazepam [J].
Marin, RH ;
Pérez, MF ;
Duero, DG ;
Ramirez, OA .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1999, 64 (03) :473-477