Neuroleptics differentially modulate central dopamine d1-receptor binding

The effect of the classical neuroleptic, fluphenazine, on dopamine D1-receptor binding was examined in different regions of the basal ganglia. Whereas exposure to fluphenazine for 18 months reduced [125I]SCH-23982 binding to D1-receptors in the caudate putamen, nucleus accumbens and olfactory tuberc...

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Autor principal: Johnson, A.E
Otros Autores: Coirini, H., Källström, L., Gunne, L.M, Wiesel, F.A
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 1995
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100 1 |a Johnson, A.E. 
245 1 0 |a Neuroleptics differentially modulate central dopamine d1-receptor binding 
260 |c 1995 
270 1 0 |m Johnson, A.E.; Department of Psychiatry, University Hospital, Uppsala University, Uppsala, S-750 17, Sweden 
506 |2 openaire  |e Política editorial 
504 |a Wiesel, F.-A., (1994) Brit J Paychiet, 184, pp. 65-70 
504 |a Angulo, J.A., McEwen, B.S., (1994) Brain Res Rav, 19, pp. 1-28 
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504 |a Anderson, K.D., Reiner, A., (1991) Brain Res, 568, pp. 235-243 
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520 3 |a The effect of the classical neuroleptic, fluphenazine, on dopamine D1-receptor binding was examined in different regions of the basal ganglia. Whereas exposure to fluphenazine for 18 months reduced [125I]SCH-23982 binding to D1-receptors in the caudate putamen, nucleus accumbens and olfactory tubercle, binding in the entopeduncular nucleus was enhanced after fluphenazine treatment. Competition studies indicated that the region-dependent changes in [125I]SCH-23982 binding after fluphenazine exposure were not due to differences in the affinity of fluphenazine or other dopamine ligands for D1-binding sites. These data suggest that in addition to modulating striatal function, classical neuroleptics may also alter neurotransmission in the basal ganglia by enhancing dopamine receptor binding in the entopeduncular nucleus. © Rapid Communications of Oxford Ltd.  |l eng 
593 |a Instituto de Biología y Medicina Experimental, Buenos Aires, 1428, Argentina 
593 |a Department of Psychiatry, University Hospital, Uppsala University, Uppsala, S-750 17, Sweden 
690 1 0 |a BASAL GANGLIA 
690 1 0 |a D1-RECEPTORS 
690 1 0 |a DOPAMINE 
690 1 0 |a ENTOPEDUNCULAR NUCLEUS 
690 1 0 |a ENTOPEDUNCULAR NUCLEUS 
690 1 0 |a EXTRAPYRAMIDAL MOTOR SYSTEM 
690 1 0 |a FLUPHENAZINE 
690 1 0 |a NEUROLEPTIC 
690 1 0 |a STRIATUM 
690 1 0 |a [125I]SCH-23982 
690 1 0 |a 2 DIPROPYLAMINO 7 HYDROXYTETRALIN 
690 1 0 |a 2,3,4,5 TETRAHYDRO 7,8 DIHYDROXY 1 PHENYL 1H 3 BENZAZEPINE 
690 1 0 |a 2,3,4,5 TETRAHYDRO 8 IODO 3 METHYL 5 PHENYL 1H 3 BENZAZEPIN 7 OL 
690 1 0 |a 8 CHLORO 2,3,4,5 TETRAHYDRO 3 METHYL 5 PHENYL 1H 3 BENZAZEPIN 7 OL HYDROGEN MALEATE 
690 1 0 |a CLOZAPINE 
690 1 0 |a DOPAMINE 
690 1 0 |a DOPAMINE 1 RECEPTOR 
690 1 0 |a FLUPHENAZINE 
690 1 0 |a NEUROLEPTIC AGENT 
690 1 0 |a RACLOPRIDE 
690 1 0 |a ANIMAL EXPERIMENT 
690 1 0 |a ANIMAL TISSUE 
690 1 0 |a ARTICLE 
690 1 0 |a BRAIN REGION 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a CORPUS STRIATUM 
690 1 0 |a ENTOPEDUNCULAR NUCLEUS 
690 1 0 |a FEMALE 
690 1 0 |a INTRAMUSCULAR DRUG ADMINISTRATION 
690 1 0 |a NONHUMAN 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a RAT 
690 1 0 |a RECEPTOR BINDING 
690 1 0 |a SUBSTANTIA NIGRA 
690 1 0 |a ANIMAL 
690 1 0 |a ANTIPSYCHOTIC AGENTS 
690 1 0 |a AUTORADIOGRAPHY 
690 1 0 |a BASAL GANGLIA 
690 1 0 |a BINDING, COMPETITIVE 
690 1 0 |a DOPAMINE ANTAGONISTS 
690 1 0 |a FEMALE 
690 1 0 |a IODINE RADIOISOTOPES 
690 1 0 |a RATS 
690 1 0 |a RATS, SPRAGUE-DAWLEY 
690 1 0 |a RECEPTORS, DOPAMINE D1 
690 1 0 |a SCH-23390 
653 0 0 |a sch 23388; sch 23390; sch 23982, new england nuclear, Sweden; skf 38393 
700 1 |a Coirini, H. 
700 1 |a Källström, L. 
700 1 |a Gunne, L.M. 
700 1 |a Wiesel, F.A. 
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