Literature DB >> 26325040

Synthesis and characterization of a dual kappa-delta opioid receptor agonist analgesic blocking cocaine reward behavior.

András Váradi1, Gina F Marrone1, Shainnel O Eans2, Michelle L Ganno2, Joan J Subrath1, Valerie Le Rouzic1, Amanda Hunkele1, Gavril W Pasternak1, Jay P McLaughlin2, Susruta Majumdar1.   

Abstract

3-Iodobenzoyl naltrexamine (n class="Chemical">IBNtxA) is a potent analgesic belonging to the pharmacologically diverse 6β-amidoepoxymorphinan group of opioids. We present the synthesis and pharmacological evaluation of five analogs of IBNtxA. The scaffold of IBNtxA was modified by removing the 14-hydroxy group, incorporating a 7,8 double bond and various N-17 alkyl substituents. The structural modifications resulted in analogs with picomolar affinities for opioid receptors. The lead compound (MP1104) was found to exhibit approximately 15-fold greater antinociceptive potency (ED50 = 0.33 mg/kg) compared with morphine, mediated through the activation of kappa- and delta-opioid receptors. Despite its kappa agonism, this lead derivative did not cause place aversion or preference in mice in a place-conditioning assay, even at doses 3 times the analgesic ED50. However, pretreatment with the lead compound prevented the reward behavior associated with cocaine in a conditioned place preference assay. Together, these results suggest the promise of dual acting kappa- and delta-opioid receptor agonists as analgesics and treatments for cocaine addiction.

Entities:  

Keywords:  IBNtxA; MP1104; Opioid analgesics; cocaine addiction; delta; kappa

Mesh:

Substances:

Year:  2015        PMID: 26325040      PMCID: PMC4651729          DOI: 10.1021/acschemneuro.5b00153

Source DB:  PubMed          Journal:  ACS Chem Neurosci        ISSN: 1948-7193            Impact factor:   4.418


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