ALPHA-1-ADRENORECEPTOR AND ALPHA-2-ADRENORECEPTOR ANTAGONISTS DIFFERENTIALLY INFLUENCE LOCOMOTOR AND STEREOTYPED BEHAVIOR INDUCED BY D-AMPHETAMINE AND APOMORPHINE IN THE RAT

被引:106
作者
DICKINSON, SL
GADIE, B
TULLOCH, IF
机构
关键词
D O I
10.1007/BF02180034
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
引用
收藏
页码:521 / 527
页数:7
相关论文
共 37 条
[1]   SELECTIVE BLOCKADE OF BRAIN ALPHA-2-AUTORECEPTORS BY YOHIMBINE - EFFECTS ON MOTOR-ACTIVITY AND ON TURNOVER OF NORADRENALINE AND DOPAMINE [J].
ANDEN, NE ;
PAUKSENS, K ;
SVENSSON, K .
JOURNAL OF NEURAL TRANSMISSION, 1982, 55 (02) :111-120
[2]  
CLINESCHMIDT BV, 1979, ARCH INT PHARMACOD T, V242, P59
[3]   CHARACTERIZATION OF MECHANISMS FOR HYPERACTIVITY INDUCTION FROM NUCLEUS ACCUMBENS BY PHENYLETHYLAMINE DERIVATIVES [J].
COSTALL, B ;
NAYLOR, RJ ;
PINDER, RM .
PSYCHOPHARMACOLOGY, 1976, 48 (02) :225-231
[4]   STEREOTYPED BEHAVIOR PATTERNS AND HYPERACTIVITY INDUCED BY AMPHETAMINE AND APOMORPHINE AFTER DISCRETE 6-HYDROXYDOPAMINE LESIONS OF EXTRAPYRAMIDAL AND MESOLIMBIC NUCLEI [J].
COSTALL, B ;
MARSDEN, CD ;
NAYLOR, RJ ;
PYCOCK, CJ .
BRAIN RESEARCH, 1977, 123 (01) :89-111
[5]   PHARMACOLOGICAL AND ANATOMICAL SUBSTRATES OF AMPHETAMINE RESPONSE IN RAT [J].
CREESE, I ;
IVERSEN, SD .
BRAIN RESEARCH, 1975, 83 (03) :419-436
[6]   DEPRESSION OF EXPLORATORY ACTIVITY BY CLONIDINE IN RATS AS A MODEL FOR THE DETECTION OF RELATIVE PRESYNAPTIC AND POSTSYNAPTIC CENTRAL NORADRENERGIC RECEPTOR SELECTIVITY OF ALPHA-ADRENOLYTIC DRUGS [J].
DELINISTULA, A ;
BAUMANN, P ;
BUCH, O .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1979, 307 (02) :115-122
[7]  
DICKINSON S L, 1986, British Journal of Pharmacology, V89, p872P
[8]   ROLES OF DOPAMINE AND 5-HYDROXYTRYPTAMINE IN STEREOTYPED AND NON-STEREOTYPED BEHAVIOR [J].
DICKINSON, SL ;
CURZON, G .
NEUROPHARMACOLOGY, 1983, 22 (07) :805-812
[9]  
DREW GM, 1979, BRIT J PHARMACOL, V67, P133
[10]   MODIFICATION OF AMPHETAMINE-INDUCED STEREOTYPY IN RATS FOLLOWING INHIBITION OF NORADRENALINE RELEASE BY FLA-136 [J].
GRABOWSKAANDEN, M .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1977, 29 (09) :566-567