Subsensitivity to dopaminergic drugs in periadolescent rats: a behavioral and neurochemical analysis

被引:156
作者
Bolanos, CA [1 ]
Glatt, SJ [1 ]
Jackson, D [1 ]
机构
[1] Northeastern Univ, Dept Psychol, Boston, MA 02115 USA
来源
DEVELOPMENTAL BRAIN RESEARCH | 1998年 / 111卷 / 01期
关键词
acetylcholine release; amphetamine; development; dopamine; striatum;
D O I
10.1016/S0165-3806(98)00116-3
中图分类号
Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
It has been reported that post-natal day (PD) 30-40 rats respond differently to the behavioral effects of dopaminergic drugs when compared to younger or older rats. In this study, the behavioral effects of amphetamine (AMPH) on motor behavior and the effects of dopaminergic drugs on striatal acelylcholine (ACh) release were evaluated in periadolescent (PD35) and adult rats. AMPH increased dopamine (DA)-mediated motor behaviors (locomotor activity and stereotypy) in periadolescent and adult rats; however, these responses were of a lesser magnitude in periadolescent rats. In adult rats, cocaine and nomifensine inhibited ACh overflow in a dose-dependent manner. In periadolescent rats, ACh overflow was maximally inhibited at a lower drug concentration (5 mu M) than in adult rats (10 mu M) signifying increased sensitivity in these rats. Apomorphine inhibited ACh overflow in a dose-dependent fashion in slices from adult rats. In contrast, apomorphine did not consistently inhibit ACh overflow in striatal slices prepared from periadolescent rats. Collectively, the results of this study demonstrate behavioral subsensitivity to AMPH in periadolescent rats. Examination of the effects of DA reuptake blockers on DA modulation of striatal cholinergic neurons failed to reveal a corresponding subsensitivity. In fact, ACh release was more sensitive to DA reuptake blockers in periadolescent rats. This latter finding suggests that undisclosed factors override dopaminergic modulation of striatal neurons in the mediation of behavior in periadolescent rats. We propose that during periadolescence, DA transmission is transiently elevated. This results in post-synaptic supersensitivity of cholinergic receptors and consequently induces behavioral subsensitivity when challenged with dopaminergic drugs. Increased cholinergic tone may mediate behavioral subsensitivity despite drug-induced elevations in DA. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:25 / 33
页数:9
相关论文
共 42 条
[1]
THE ONTOGENY OF APOMORPHINE-INDUCED ALTERATIONS OF NEOSTRIATAL DOPAMINE RELEASE - EFFECTS ON SPONTANEOUS RELEASE [J].
ANDERSEN, SL ;
GAZZARA, RA .
JOURNAL OF NEUROCHEMISTRY, 1993, 61 (06) :2247-2255
[2]
ARNFRED T, 1968, ACTA PHARMACOL TOX, V26, P384
[3]
DIFFERENTIAL EFFECTS OF D-AMPHETAMINE IN MATURE AND IMMATURE RATS [J].
BAUER, RH ;
DUNCAN, DL .
PHYSIOLOGICAL PSYCHOLOGY, 1975, 3 (03) :312-316
[4]
THE ROLE OF DOPAMINE IN LOCOMOTOR-ACTIVITY AND LEARNING [J].
BENINGER, RJ .
BRAIN RESEARCH REVIEWS, 1983, 6 (02) :173-196
[5]
AMPHETAMINE, COCAINE, PHENCYCLIDINE AND NOMIFENSINE INCREASE EXTRACELLULAR DOPAMINE CONCENTRATIONS PREFERENTIALLY IN THE NUCLEUS ACCUMBENS OF FREELY MOVING RATS [J].
CARBONI, E ;
IMPERATO, A ;
PEREZZANI, L ;
DICHIARA, G .
NEUROSCIENCE, 1989, 28 (03) :653-661
[6]
REVIEW - D1 DOPAMINE RECEPTOR - THE SEARCH FOR A FUNCTION - A CRITICAL-EVALUATION OF THE D1/D2 DOPAMINE RECEPTOR CLASSIFICATION AND ITS FUNCTIONAL IMPLICATIONS [J].
CLARK, D ;
WHITE, FJ .
SYNAPSE, 1987, 1 (04) :347-388
[7]
ONTOGENIC EFFECTS OF EEDQ ON AMPHETAMINE-INDUCED BEHAVIORS OF RATS - ROLE OF PRESYNAPTIC PROCESSES [J].
CRAWFORD, CA ;
MCDOUGALL, SA ;
BARDO, MT .
PSYCHOPHARMACOLOGY, 1994, 116 (02) :152-160
[8]
DeBoer P, 1996, J PHARMACOL EXP THER, V277, P775
[9]
INDEPENDENT GABAERGIC AND CHOLINERGIC MODULATION OF APOMORPHINE-INDUCED STEREOTYPED REARING IN THE RAT [J].
DECSI, L ;
NAGY, J .
NEUROPHARMACOLOGY, 1988, 27 (03) :281-285
[10]
DIFFERENTIAL ONTOGENY OF FUNCTIONAL DOPAMINE AND MUSCARINIC RECEPTORS MEDIATING PRESYNAPTIC INHIBITION OF NEUROTRANSMITTER RELEASE AND POSTSYNAPTIC REGULATION OF ADENYLATE-CYCLASE ACTIVITY IN RAT STRIATUM [J].
DEVRIES, TJ ;
MULDER, AH ;
SCHOFFELMEER, ANM .
DEVELOPMENTAL BRAIN RESEARCH, 1992, 66 (01) :91-96