A Chimeric Vesicular Monoamine Transporter Dissociates Sensitivity to Tetrabenazine and Unsubstituted Aromatic Amines

Advances in Pharmacology

Volumn 42, Issue C, 1997, Pages 227-232

  Erickson, J D ^a  

^a LOUISIANA STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 26844565125     PISSN: 10543589     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S1054-3589(08)60734-6     Document Type: Article

References (5)

1. Erickson J.D., Schäfer M.K.-H., Bonnet T.I., Eiden L.E., and Weihe E. Distinct pharmacological properties and distribution in neurons and endocrine cells of two isoforms of the human vesicular monoamine transporter. Proc. Natl. Acad. Sci. U.S.A. 93 (1996) 5166-5171
2. 1H-histamine by the neuronal isoform of the vesicular monoamine transporter. J. Mol. Neurosci. 6 (1995) 277-287
3. Peter D., Vu T., and Edwards R.H. Chimeric vesicular monoamine transporters identify structural domains that influence substrate affinity and sensitivity to tetrabenazine. J. Biol. Chem. 271 (1996) 2979-2986
4. Erickson J.D., Eiden L.E., and Hoffman B.J. Expression cloning of a reserpine-sensitive vesicular monoamine transporter. Proc. Natl. Acad. Sci. U.S.A. 89 (1992) 10993-10997
5. Sievert M.D., and Ruoho A.E. Identification of drug binding sites on the synaptic vesicle monoamine translocator. FASEB J. 10 (1996) A1233 (#1350)