Interaction of 1-methyl-4-phenylpyridinium ion and tyramine with a site putatively involved in the striatal vesicular release of dopamine
Author:
Publisher
Wiley
Subject
Pharmacology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1476-5381.1991.tb12470.x/fullpdf
Reference10 articles.
1. The non-competitive NMDA-receptor antagonist MK-801 prevents the massive release of glutamate and aspartate from rat striatum induced by 1-methyl-4-phenylpyridinium (MPP+);CARBONI;Neurosci. Lett.,1990
2. Energy-driven uptake of the neurotoxin 1-methyl-4-phenylpyridinium into chromaffin granules via the catecholamine transporter;DANIELS;J. Biol. Chem.,1988
3. [3H]1-Methyl-4-phenyl-2,3-dihydropyridinium ion binding sites in mouse brain: pharmacological and biological characterization;ZOMPO;J. Neurochem.,1990
4. In vivo mechanisms underlying dopamine release from nigrostriatal terminals: II. Studies using potassium and tyramine;FAIRBROTHER;J. Neurochem.,1990
5. Radioligands of the vesicular monoamine transporter and their use as markers of monoamine storage vesicles;HENRY;Biochem. Pharmacol.,1989
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