D2 and D1 dopaminergic activity of 7-OH-DPAT
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Clinical Neurology,Molecular Biology,General Neuroscience
Reference27 articles.
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3. Comparison between the pharmacology of dopamine receptors mediating the inhibition of cell firing in rat brain slices through substantia nigra pars compacta and ventral tegmental area;Bowery;Br. J. Pharmacol.,1994
4. Behavioral effects of the putative D-3 dopamine receptor agonist 7-OH-DPAT in relation to other ‘D-2 like’ agonists;Daly;Neuropharmacology,1993
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1. Stimulation of 5-HT1A receptor with 8-OH-DPAT inhibits hydrogen peroxide-induced neurotoxicity in cultured rat cortical cells;Pharmacological Research;2005-03
2. Lack of a role for the D3 receptor in clozapine induction of c-fos demonstrated in D3 dopamine receptor-deficient mice;Neuroscience;1999-05
3. Both dopamine and the putative dopamine D3 receptor antagonist PNU-99194A induce a biphasic inhibition of phorbol ester-stimulated arachidonic acid release from CHO cells transfected with the dopamine D3 receptor;Life Sciences;1999-02
4. PNU-99194A: A Preferential Dopamine D3 Receptor Antagonist;CNS Drug Reviews;1998-03
5. D1 dopamine receptor activity of anti-Parkinsonian drugs;Life Sciences;1997-03
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