Abstract
The activity of neurones in the zona compacta of the rat substantia nigra was recorded extracellularly in vitro. Dopamine produced a dose-dependent depression of firing, threshold doses being in the 3 microM range. The inhibitory effects of dopamine were antagonized by (-)-sulpiride (pA2 7.5), haloperidol (pA2 8.4) and cis-flupenthixol (pA2 6.9). The actions of gamma-aminobutyric acid (GABA) were not affected by these compounds. The gradients of Schild plots of data for (-)-sulpiride were less than unity while those for haloperidol and cis-flupenthixol were greater than unity, which suggests that the antagonism was not competitive. This is discussed with regard to the use of a bioassay system in the analysis of the effects of antagonists. Haloperidol and (-)-sulpiride were found to have similar potencies, as dopamine receptor antagonists, to those predicted from biochemical and clinical efficacy studies, but cis-flupenthixol was less potent than expected.
MeSH Terms
Action Potentials/drug effects
Animals
Antipsychotic Agents/pharmacology
Dopamine/pharmacology
Dopamine Antagonists
Flupenthixol/pharmacology
Haloperidol/pharmacology
In Vitro Techniques
Male
Neurons/physiology
Rats
Receptors, Dopamine/drug effects,physiology
Stereoisomerism
Substantia Nigra/physiology
Sulpiride/pharmacology
Chemicals
Antipsychotic Agents
Dopamine Antagonists
Receptors, Dopamine
Sulpiride
Flupenthixol
Haloperidol
Dopamine
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Pinnock R D
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19 references, click to expand
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