Discovery of Novel Delta Opioid Receptor (DOR) Inverse Agonist and Irreversible (Non-Competitive) Antagonists

被引:11
作者
Tanguturi, Parthasaradhireddy [1 ]
Pathak, Vibha [2 ]
Zhang, Sixue [2 ]
Moukha-Chafiq, Omar [2 ]
Augelli-Szafran, Corinne E. [2 ]
Streicher, John M. [1 ]
机构
[1] Univ Arizona, Dept Pharmacol, Coll Med, Tucson, AZ 85724 USA
[2] Southern Res Inst, Dept Chem, Div Drug Discovery, Birmingham, AL 35205 USA
关键词
delta opioid receptor; inverse agonist; irreversible antagonist; non-competitive antagonist; molecular pharmacology; ANALOGS; POTENT; ANTINOCICEPTION; BINDING;
D O I
10.3390/molecules26216693
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The delta opioid receptor (DOR) is a crucial receptor system that regulates pain, mood, anxiety, and similar mental states. DOR agonists, such as SNC80, and DOR-neutral antagonists, such as naltrindole, were developed to investigate the DOR in vivo and as potential therapeutics for pain and depression. However, few inverse agonists and non-competitive/irreversible antagonists have been developed, and none are widely available. This leaves a gap in our pharmacological toolbox and limits our ability to investigate the biology of this receptor. Thus, we designed and synthesized the novel compounds SRI-9342 as an irreversible antagonist and SRI-45128 as an inverse agonist. These compounds were then evaluated in vitro for their binding affinity by radioligand binding, their functional activity by S-35-GTP gamma S coupling, and their cAMP accumulation in cells expressing the human DOR. Both compounds demonstrated high binding affinity and selectivity at the DOR, and both displayed their hypothesized molecular pharmacology of irreversible antagonism (SRI-9342) or inverse agonism (SRI-45128). Together, these results demonstrate that we have successfully designed new inverse agonists and irreversible antagonists of the DOR based on a novel chemical scaffold. These new compounds will provide new tools to investigate the biology of the DOR or even new potential therapeutics.
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页数:13
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共 31 条
[1]   Synthesis, opioid receptor binding, and bioassay of naltrindole analogues substituted in the indolic benzene moiety [J].
Ananthan, S ;
Johnson, CA ;
Carter, RL ;
Clayton, SD ;
Rice, KC ;
Xu, H ;
Davis, P ;
Porreca, F ;
Rothman, RB .
JOURNAL OF MEDICINAL CHEMISTRY, 1998, 41 (15) :2872-2881
[2]   Endogenous opiates and behavior: 2013 [J].
Bodnar, Richard J. .
PEPTIDES, 2014, 62 :67-136
[3]   The Opioid System in Temporal Lobe Epilepsy: Functional Role and Therapeutic Potential [J].
Burtscher, Johannes ;
Schwarzer, Christoph .
FRONTIERS IN MOLECULAR NEUROSCIENCE, 2017, 10
[4]   Opioid ligands with mixed properties from substituted enantiomeric N-phenethyl-5-phenylmorphans.: Synthesis of a μ-agonist δ-antagonist and δ-inverse agonists [J].
Cheng, Kejun ;
Kim, In Jong ;
Lee, Mei-Jing ;
Adah, Steven A. ;
Raymond, Tyler J. ;
Bilsky, Edward J. ;
Aceto, Mario D. ;
May, Everette L. ;
Harris, Louis S. ;
Coop, Andrew ;
Dersch, Christina M. ;
Rothman, Richard B. ;
Jacobson, Arthur E. ;
Rice, Kenner C. .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2007, 5 (08) :1177-1190
[5]   Elucidating the active δ-opioid receptor crystal structure with peptide and small-molecule agonists [J].
Claff, Tobias ;
Yu, Jing ;
Blais, Veronique ;
Patel, Nilkanth ;
Martin, Charlotte ;
Wu, Lijie ;
Han, Gye Won ;
Holleran, Brian J. ;
Van der Poorten, Olivier ;
White, Kate L. ;
Hanson, Michael A. ;
Sarret, Philippe ;
Gendron, Louis ;
Cherezov, Vadim ;
Katritch, Vsevolod ;
Ballet, Steven ;
Liu, Zhi-Jie ;
Mueller, Christa E. ;
Stevens, Raymond C. .
SCIENCE ADVANCES, 2019, 5 (11) :eaax9115
[6]   ANTAGONISTS WITH NEGATIVE INTRINSIC ACTIVITY AT DELTA-OPIOID RECEPTORS COUPLED TO GTP-BINDING PROTEINS [J].
COSTA, T ;
HERZ, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (19) :7321-7325
[7]   Receptor-selective antagonism of opioid antinociception in female versus male rats [J].
Craft, RM ;
Tseng, AH ;
McNiel, DM ;
Furness, MS ;
Rice, KC .
BEHAVIOURAL PHARMACOLOGY, 2001, 12 (08) :591-602
[8]   Na+ modulation, inverse agonism, and anorectic potency of 4-phenylpiperidine opioid antagonists [J].
Emmerson, PJ ;
McKinzie, JH ;
Surface, PL ;
Suter, TM ;
Mitch, CH ;
Statnick, MA .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2004, 494 (2-3) :121-130
[9]   Molecular control of δ-opioid receptor signalling [J].
Fenalti, Gustavo ;
Giguere, Patrick M. ;
Katritch, Vsevolod ;
Huang, Xi-Ping ;
Thompson, Aaron A. ;
Cherezov, Vadim ;
Roth, Bryan L. ;
Stevens, Raymond C. .
NATURE, 2014, 506 (7487) :191-196
[10]   o-naphthalenedicarboxaldehyde derivative of 7′-aminonaltrindole as a selective δ-opioid receptor affinity label [J].
Haris, Sarika Prabhu ;
Zhang, Yan ;
Le Bourdonnec, Bertrand ;
McCurdy, Christopher R. ;
Portoghese, Philip S. .
JOURNAL OF MEDICINAL CHEMISTRY, 2007, 50 (14) :3392-3396