Literature DB >> 15999263

Look before leaping: combined opioids may not be the rave.

Mellar P Davis1, Susan B LeGrand, Ruth Lagman.   

Abstract

The use of combinations of potent opioids is a common clinical practice. The addition of one potent opioid to another has been recommended to reduce opioid side effects, improve pain control, and limit dose escalation of the first opioid. The advantages of using combined opioids have been reported to be relative to differences in receptor activation versus endocytosis (RAVE). However, the advantages and detriment to combining opioids are related to naturally occurring opioid receptor dimers. Dimers and oligomers result in a unique opioid pharmacodynamics which influence opioid binding, G protein interactions, desensitization, receptor trafficking, and endocytosis. The pharmacodynamics of dimers may lead to positive or negative cooperativity when two opioids are combined. The use of multiple opioids in practice can lead to increased risk for dosing errors, reduced patient compliance, increased drug interactions and cost. Opioid combinations should not be used until prospective randomized trials clarify the benefits and safety.

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Year:  2005        PMID: 15999263     DOI: 10.1007/s00520-005-0839-y

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  45 in total

1.  Recycling and resensitization of delta opioid receptors.

Authors:  N Trapaidze; I Gomes; M Bansinath; L A Devi
Journal:  DNA Cell Biol       Date:  2000-04       Impact factor: 3.311

Review 2.  Opioid receptor regulation.

Authors:  Mark von Zastrow
Journal:  Neuromolecular Med       Date:  2004       Impact factor: 3.843

3.  Gaps and junctions between clinical experience and theoretical framework in the use of opioids.

Authors:  Marianne Kloke
Journal:  Support Care Cancer       Date:  2004-11       Impact factor: 3.603

4.  The mu opioid irreversible antagonist beta-funaltrexamine differentiates the discriminative stimulus effects of opioids with high and low efficacy at the mu opioid receptor.

Authors:  D Morgan; M J Picker
Journal:  Psychopharmacology (Berl)       Date:  1998-11       Impact factor: 4.530

5.  Opioid receptor endocytosis and activation of MAP kinase pathway.

Authors:  N Trapaidze; I Gomes; S Cvejic; M Bansinath; L A Devi
Journal:  Brain Res Mol Brain Res       Date:  2000-03-29

Review 6.  Regulated endocytosis of opioid receptors: cellular mechanisms and proposed roles in physiological adaptation to opiate drugs.

Authors:  Mark von Zastrow; Adena Svingos; Helena Haberstock-Debic; Chris Evans
Journal:  Curr Opin Neurobiol       Date:  2003-06       Impact factor: 6.627

7.  Receptor endocytosis counteracts the development of opioid tolerance.

Authors:  Thomas Koch; Antje Widera; Katharina Bartzsch; Stefan Schulz; Lars-Ove Brandenburg; Nicole Wundrack; Andrea Beyer; Gisela Grecksch; Volker Höllt
Journal:  Mol Pharmacol       Date:  2004-10-08       Impact factor: 4.436

8.  Addition of a second opioid may improve opioid response in cancer pain: preliminary data.

Authors:  Sebastiano Mercadante; Patrizia Villari; Patrizia Ferrera; Alessandra Casuccio
Journal:  Support Care Cancer       Date:  2004-11       Impact factor: 3.603

9.  Opioid peptide receptor studies. 17. Attenuation of chronic morphine effects after antisense oligodeoxynucleotide knock-down of RGS9 protein in cells expressing the cloned Mu opioid receptor.

Authors:  Heng Xu; Xiaoying Wang; Jun Wang; Richard B Rothman
Journal:  Synapse       Date:  2004-06-01       Impact factor: 2.562

Review 10.  Agonist-induced regulation and trafficking of kappa opioid receptors.

Authors:  Lee-Yuan Liu-Chen
Journal:  Life Sci       Date:  2004-06-18       Impact factor: 5.037

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  1 in total

1.  The role of methadone in opioid rotation-a Polish experience.

Authors:  Wojciech Leppert
Journal:  Support Care Cancer       Date:  2008-11-29       Impact factor: 3.603

  1 in total

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