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      Exploring the first Rimonabant analog-opioid peptide hybrid compound, as bivalent ligand for CB1 and opioid receptors

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          Abstract

          Cannabinoid (CB) and opioid systems are both involved in analgesia, food intake, mood and behavior. Due to the co-localization of µ-opioid (MOR) and CB1 receptors in various regions of the central nervous system (CNS) and their ability to form heterodimers, bivalent ligands targeting to both these systems may be good candidates to investigate the existence of possible cross-talking or synergistic effects, also at sub-effective doses. In this work, we selected from a small series of new Rimonabant analogs one CB1R reverse agonist to be conjugated to the opioid fragment Tyr-D-Ala-Gly-Phe-NH 2. The bivalent compound ( 9) has been used for in vitro binding assays, for in vivo antinociception models and in vitro hypothalamic perfusion test, to evaluate the neurotransmitters release.

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          Most cited references42

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          SR141716A, a potent and selective antagonist of the brain cannabinoid receptor.

          SR141716A is the first selective and orally active antagonist of the brain cannabinoid receptor. This compound displays nanomolar affinity for the central cannabinoid receptor but is not active on the peripheral cannabinoid receptor. In vitro, SR141716A antagonises the inhibitory effects of cannabinoid receptor agonists on both mouse vas deferens contractions and adenylyl cyclase activity in rat brain membranes. After intraperitoneal or oral administration SR141716A antagonises classical pharmacological and behavioural effects of cannabinoid receptor agonists. This compound should prove to be a powerful tool for investigating the in vivo functions of the anandamide/cannabinoid system.
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            Scikit-learn: Machine learning in Python

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              Cannabinoid and opioid interactions: implications for opiate dependence and withdrawal.

              Withdrawal from opiates, such as heroin or oral narcotics, is characterized by a host of aversive physical and emotional symptoms. High rates of relapse and limited treatment success rates for opiate addiction have prompted a search for new approaches. For many opiate addicts, achieving abstinence may be further complicated by poly-drug use and co-morbid mental disorders. Research over the past decade has shed light on the influence of endocannabinoids (ECs) on the opioid system. Evidence from both animal and clinical studies point toward an interaction between these two systems, and suggest that targeting the EC system may provide novel interventions for managing opiate dependence and withdrawal. This review will summarize the literature surrounding the molecular effects of cannabinoids and opioids on the locus coeruleus-norepinephrine system, a key circuit implicated in the negative sequelae of opiate addiction. A consideration of the trends and effects of marijuana use in those seeking treatment to abstain from opiates in the clinical setting will also be presented. In summary, the present review details how cannabinoid-opioid interactions may inform novel interventions in the management of opiate dependence and withdrawal. Copyright © 2013 IBRO. Published by Elsevier Ltd. All rights reserved.
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                Author and article information

                Journal
                J Enzyme Inhib Med Chem
                J Enzyme Inhib Med Chem
                IENZ
                ienz20
                Journal of Enzyme Inhibition and Medicinal Chemistry
                Taylor & Francis
                1475-6366
                1475-6374
                2017
                18 January 2017
                : 32
                : 1
                : 444-451
                Affiliations
                [a ] Dipartimento di Farmacia, Università di Chieti-Pescara “G. d’Annunzio” , Chieti, Italy;
                [b ] Dipartimento di Chimica e Tecnologie del Farmaco, Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Sapienza Università di Roma , Roma, Italy;
                [c ] Dipartimento del Farmaco, Istituto Superiore di Sanità , Rome, Italy;
                [d ] Dipartimento di Farmacia, Università di Napoli “Federico II” , Naples, Italy;
                [e ] Institute of Biochemistry, Biological Research Centre, Hungarian Academy of Sciences , Szeged, Hungary;
                [f ] Dipartimento di Chimica e Tecnologie del Farmaco, Rome Center for Molecular Design, Sapienza Università di Roma , Roma, Italy;
                [g ] Alchemical Dynamics s.r.l , Roma, Italy
                Author notes
                CONTACT Romano Silvestri romano.silvestri@ 123456uniroma1.it Dipartimento di Chimica e Tecnologie del Farmaco, Sapienza Università di Roma , Piazzale Aldo Moro 5, I-00185Roma, Italy

                Supplemental data for this article can be accessed here.

                This article was originally published with errors. This version has been corrected. Please see Corrigendum ( http://dx.doi.org/10.1080/14756366.2017.1324597)

                Article
                1260565
                10.1080/14756366.2016.1260565
                6009935
                28097916
                bd0c263d-35f1-4b5f-9c0f-f49c70b499a1
                © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 13 August 2016
                : 31 October 2016
                : 08 November 2016
                Page count
                Pages: 8, Words: 4198
                Categories
                Short Communication

                Pharmaceutical chemistry
                cannabinoid receptor cb1r,rimonabant,opioids,bivalent ligand,pain
                Pharmaceutical chemistry
                cannabinoid receptor cb1r, rimonabant, opioids, bivalent ligand, pain

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