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Journal Abstract Search

251 related items for PubMed ID: 12151036

  • 1. Effects of opioid antagonists on unconditioned and conditioned hyperactivity to morphine.
    Rauhut AS, Gehrke BJ, Phillips SB, Bardo MT.
    Pharmacol Biochem Behav; 2002 Oct; 73(3):611-22. PubMed ID: 12151036
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  • 2. Different roles of mu-, delta- and kappa-opioid receptors in ethanol-associated place preference in rats exposed to conditioned fear stress.
    Matsuzawa S, Suzuki T, Misawa M, Nagase H.
    Eur J Pharmacol; 1999 Feb 26; 368(1):9-16. PubMed ID: 10096764
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  • 3. Naltrexone in vivo protects mu receptors from inactivation by beta-funaltrexamine, but not kappa receptors from inactivation by nor-binaltorphimine.
    Paronis CA, Waddell AB, Holtzman SG.
    Pharmacol Biochem Behav; 1993 Dec 26; 46(4):813-7. PubMed ID: 8309960
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  • 4. Comparison of the peripheral and central effects of the opioid agonists loperamide and morphine in the formalin test in rats.
    Shannon HE, Lutz EA.
    Neuropharmacology; 2002 Feb 26; 42(2):253-61. PubMed ID: 11804622
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  • 10. Effects of opioid receptor antagonists on the effects of i.v. morphine on carrageenin evoked c-Fos expression in the superficial dorsal horn of the rat spinal cord.
    Catheline G, Le Guen S, Besson JM.
    Brain Res; 1999 Apr 03; 824(1):105-11. PubMed ID: 10095048
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  • 12. Assessment of SNC 80 and naltrindole within a conditioned taste aversion design.
    Hutchinson AC, Simpson GR, Randall JF, Zhang X, Calderon SN, Rice KC, Riley AL.
    Pharmacol Biochem Behav; 2000 Aug 03; 66(4):779-87. PubMed ID: 10973516
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  • 13. Discriminative stimulus properties of morphine mediated by mu 1-opioid receptors.
    Suzuki T, Mori T, Tsuji M, Misawa M, Nagase H.
    Eur J Pharmacol; 1995 Sep 15; 284(1-2):195-8. PubMed ID: 8549626
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  • 14. Differential involvement of opioid receptors in intrathecal butorphanol-induced analgesia: compared to morphine.
    Wongchanapai W, Tsang BK, He Z, Ho IK.
    Pharmacol Biochem Behav; 1998 Mar 15; 59(3):723-7. PubMed ID: 9512078
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  • 15. Role of delta-opioid receptors in mediating the aversive stimulus effects of morphine withdrawal in the rat.
    Funada M, Schutz CG, Shippenberg TS.
    Eur J Pharmacol; 1996 Apr 04; 300(1-2):17-24. PubMed ID: 8741160
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  • 16. Intramuscular administration of morphine reduces mustard-oil-induced craniofacial-muscle pain behavior in lightly anesthetized rats.
    Han SR, Lee MK, Lim KH, Yang GY, Jeon HJ, Ju JS, Yoon YW, Kim SK, Ahn DK.
    Eur J Pain; 2008 Apr 04; 12(3):361-70. PubMed ID: 17768078
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  • 17. Methocinnamox is a potent, long-lasting, and selective antagonist of morphine-mediated antinociception in the mouse: comparison with clocinnamox, beta-funaltrexamine, and beta-chlornaltrexamine.
    Broadbear JH, Sumpter TL, Burke TF, Husbands SM, Lewis JW, Woods JH, Traynor JR.
    J Pharmacol Exp Ther; 2000 Sep 04; 294(3):933-40. PubMed ID: 10945843
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  • 18. mu- but not delta- and kappa-opioid receptors in the ventrolateral orbital cortex mediate opioid-induced antiallodynia in a rat neuropathic pain model.
    Zhao M, Wang JY, Jia H, Tang JS.
    Brain Res; 2006 Mar 03; 1076(1):68-77. PubMed ID: 16476416
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  • 19. Opioid antagonist profile of SC nor-binaltorphimine in the formalin paw assay.
    Wettstein JG, Grouhel A.
    Pharmacol Biochem Behav; 1996 Feb 03; 53(2):411-6. PubMed ID: 8808151
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  • 20. Augmentation of spinal morphine analgesia and inhibition of tolerance by low doses of mu- and delta-opioid receptor antagonists.
    Abul-Husn NS, Sutak M, Milne B, Jhamandas K.
    Br J Pharmacol; 2007 Jul 03; 151(6):877-87. PubMed ID: 17502848
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