In vivo striatal binding of the D1 antagonist SCH 23390 is not modified by changes in dopaminergic transmission.

Abstract:

:The in vivo striatal binding of [3H]SCH 23390, an antagonist of the D1 dopamine receptors, was investigated in mice submitted to pretreatment to either decrease (gammabutyrolactone 750 mg/kg, i.p.) or, increase (3,4-dihydroxyphenylalanine (L-DOPA) 200 mg/kg i.p. plus dexamphetamine 4 mg/kg, s.c.) dopaminergic transmission. Such conditions failed to modify [3H]SCH 23390 binding. However, we observed that dopamine (at concentrations > or = 1 microM), reduced the in vitro binding of [3H]SCH 23390 in membrane fractions. These results suggest that modifications in dopamine neurotransmission do not alter the in vivo quantification of D1 receptors with [3H]SCH 23390, for example, in studies that use positron emission tomography.

journal_name

Neuropharmacology

journal_title

Neuropharmacology

authors

Thibaut F,Vaugeois JM,Bonnet JJ,Costentin J

doi

10.1016/0028-3908(95)00187-5

subject

Has Abstract

pub_date

1996-03-01 00:00:00

pages

267-72

issue

3

eissn

0028-3908

issn

1873-7064

pii

0028390895001875

journal_volume

35

pub_type

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