Binding of antiparkinsonian ergot derivatives to the dopamine receptor.

Abstract:

:The effects of bromocriptine, lisuride and apomorphine on specific binding of 3H-spiroperidol to homogenates of rat caudate nucleus were studied. (+)-Butaclamol was used to define specific binding. Bromocriptine and lisuride inhibited binding markedly, in vitro and also 30 min after in vivo injection. Bromocriptine continued to inhibit binding 24h after a single injection and also after 4 days of drug administration. Lisuride did not affect net specific binding at these periods. Apomorphine produced a mild reduction in binding after 30 min but none after 4 days. It appears that the ergot alkaloids inhibit binding of 3H-spiroperidol by binding strongly to the dopamine receptor.

journal_title

Psychopharmacology

authors

Weir RL,Hruska RE,Silbergeld EK

doi

10.1007/BF00432172

subject

Has Abstract

pub_date

1981-01-01 00:00:00

pages

119-23

issue

2

eissn

0033-3158

issn

1432-2072

journal_volume

75

pub_type

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