Characterization of N,N(Me)(2)-Dmt-Tic-OH, a delta selective opioid dipeptide antagonist

Citation
K. Monory et al., Characterization of N,N(Me)(2)-Dmt-Tic-OH, a delta selective opioid dipeptide antagonist, NEUROREPORT, 11(10), 2000, pp. 2083-2086
Citations number
19
Categorie Soggetti
Neurosciences & Behavoir
Journal title
NEUROREPORT
ISSN journal
09594965 → ACNP
Volume
11
Issue
10
Year of publication
2000
Pages
2083 - 2086
Database
ISI
SICI code
0959-4965(20000714)11:10<2083:CONADS>2.0.ZU;2-M
Abstract
N,N(Me)(2)-Dimethyl-tyrosine-1,2,3,4-tetrahydroisoquinoline-3-carboxylic ac id-OH (N,N(Me)(2)-Dmt-Tic-OH) is a very selective delta opioid dipeptide wi th elevated antagonist activity. We have radiolabelled this compound by cat alytic tritiation of the N,N(Me)(2)-Dmt(3',5'-I-2)-Tic-OH precursor. The li gand labelled rat brain membranes with a K-d value of 0.42 nM and a B-max o f 63.12 fmol/mg protein. The new tritiated ligand showed high affinity for the delta opioid receptor whereas its binding at mu and kappa opioid recept ors was weak. N,N(Me)(2)-Dmt-Tic-OH was able to inhibit the agonist-stimula ted binding of the non-hydrolysable GTP analogue [S-35]GTP gamma S, thus at tenuating the activation of G proteins via opioid receptors. This simple op ioid dipeptide in both normal and labelled form may serve as a useful tool to study delta opioid receptors in vitro and in vivo. NeuroReport 11:2083-2 086 (C) 2000 Lippincott Williams & Wilkins.