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182 related items for PubMed ID: 32154915

  • 1. Improved efficacy, tolerance, safety, and abuse liability profile of the combination of CR4056 and morphine over morphine alone in rodent models.
    Sala E, Ferrari F, Lanza M, Milia C, Sabatini C, Bonazzi A, Comi E, Borsi Franchini M, Caselli G, Rovati LC.
    Br J Pharmacol; 2020 Jul; 177(14):3291-3308. PubMed ID: 32154915
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  • 3. CR4056, a powerful analgesic imidazoline-2 receptor ligand, inhibits the inflammation-induced PKCε phosphorylation and membrane translocation in sensory neurons.
    Vellani V, Sabatini C, Milia C, Caselli G, Lanza M, Letari O, Rovati LC, Giacomoni C.
    Br J Pharmacol; 2020 Jan; 177(1):48-64. PubMed ID: 31454418
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  • 8. Endomorphin analog analgesics with reduced abuse liability, respiratory depression, motor impairment, tolerance, and glial activation relative to morphine.
    Zadina JE, Nilges MR, Morgenweck J, Zhang X, Hackler L, Fasold MB.
    Neuropharmacology; 2016 Jun; 105():215-227. PubMed ID: 26748051
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  • 9. The imidazoline I2 receptor agonist 2-BFI reduces abuse-related effects of morphine: self-administration and drug discrimination.
    Siemian JN, Woodhouse K, Liu DH, Zhang Y, Li JX.
    Psychopharmacology (Berl); 2024 Mar; 241(3):479-487. PubMed ID: 38159161
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  • 11. Attenuation of tolerance to opioid-induced antinociception and protection against morphine-induced decrease of neurofilament proteins by idazoxan and other I2-imidazoline ligands.
    Boronat MA, Olmos G, García-Sevilla JA.
    Br J Pharmacol; 1998 Sep; 125(1):175-85. PubMed ID: 9776358
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  • 12. Mu opioid receptor in microglia contributes to morphine analgesic tolerance, hyperalgesia, and withdrawal in mice.
    Reiss D, Maduna T, Maurin H, Audouard E, Gaveriaux-Ruff C.
    J Neurosci Res; 2022 Jan; 100(1):203-219. PubMed ID: 32253777
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  • 13. A new potent analgesic agent with reduced liability to produce morphine tolerance.
    Kiraly K, Caputi FF, Hanuska A, Kató E, Balogh M, Köles L, Palmisano M, Riba P, Hosztafi S, Romualdi P, Candeletti S, Ferdinandy P, Fürst S, Al-Khrasani M.
    Brain Res Bull; 2015 Aug; 117():32-8. PubMed ID: 26235542
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  • 15. Naloxone rapidly evokes endogenous kappa opioid receptor-mediated hyperalgesia in naïve mice pretreated briefly with GM1 ganglioside or in chronic morphine-dependent mice.
    Crain SM, Shen KF.
    Brain Res; 2007 Sep 05; 1167():31-41. PubMed ID: 17692296
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  • 17. Analgesic activity of ZC88, a novel N-type voltage-dependent calcium channel blocker, and its modulation of morphine analgesia, tolerance and dependence.
    Meng G, Wu N, Zhang C, Su RB, Lu XQ, Liu Y, Yun LH, Zheng JQ, Li J.
    Eur J Pharmacol; 2008 May 31; 586(1-3):130-8. PubMed ID: 18374913
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  • 20. Ultra-low-dose naloxone suppresses opioid tolerance, dependence and associated changes in mu opioid receptor-G protein coupling and Gbetagamma signaling.
    Wang HY, Friedman E, Olmstead MC, Burns LH.
    Neuroscience; 2005 May 31; 135(1):247-61. PubMed ID: 16084657
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