CNS Dopamine Receptors: Effect of Prolyl-Leucyl-Glycinamide and Solubilization
Identifieur interne : 005026 ( Main/Exploration ); précédent : 005025; suivant : 005027CNS Dopamine Receptors: Effect of Prolyl-Leucyl-Glycinamide and Solubilization
Auteurs : Ram K. Mishra [Canada]Source :
- Nutrition and Health [ 0260-1060 ] ; 1984.
Abstract
In order to elucidate the mechanism of interaction of a peptide L-prolylleucyl-glycinamide (PLC) with dopamine receptors, we have studied the action of PLC on dopamine receptors in various brain regions. The results support the hypothesis that specific PLC binding sites exist in the central nervous system and these binding sites (receptors) have a modulatory effect on the sensitivity of dopamine receptors. It is also suggested that PLC and its active analogues warrant further vigorous and systematic clinical trials to establish their therapeutic efficacy in Parkinson's disease, neuroleptic drug induced tardive dyskinesia and related estrapyramidal motor disorders. Studies carried out on solubilized dopamine receptors and adenylate cyclase suggest that dopamine receptors sites coupled to neurolic drug action and adenylate cyclase linked receptor sites might be closely interrelated. The preliminary results on lymphocyte dopamine binding sites suggest an increase in binding in schizophrenic patients, however, receptor criteria (stereospecific binding, saturation, etc.) could not be met for these binding sites (see Rotstein et al., 1983, for details).
Url:
DOI: 10.1177/026010618400300306
Affiliations:
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<front><div type="abstract" xml:lang="en">In order to elucidate the mechanism of interaction of a peptide L-prolylleucyl-glycinamide (PLC) with dopamine receptors, we have studied the action of PLC on dopamine receptors in various brain regions. The results support the hypothesis that specific PLC binding sites exist in the central nervous system and these binding sites (receptors) have a modulatory effect on the sensitivity of dopamine receptors. It is also suggested that PLC and its active analogues warrant further vigorous and systematic clinical trials to establish their therapeutic efficacy in Parkinson's disease, neuroleptic drug induced tardive dyskinesia and related estrapyramidal motor disorders. Studies carried out on solubilized dopamine receptors and adenylate cyclase suggest that dopamine receptors sites coupled to neurolic drug action and adenylate cyclase linked receptor sites might be closely interrelated. The preliminary results on lymphocyte dopamine binding sites suggest an increase in binding in schizophrenic patients, however, receptor criteria (stereospecific binding, saturation, etc.) could not be met for these binding sites (see Rotstein et al., 1983, for details).</div>
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