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1635 related items for PubMed ID: 18374913

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Glycyl-glutamine, an endogenous beta-endorphin-derived peptide, inhibits morphine-induced conditioned place preference, tolerance, dependence, and withdrawal.
    Cavun S, Göktalay G, Millington WR.
    J Pharmacol Exp Ther; 2005 Nov 31; 315(2):949-58. PubMed ID: 16079299
    [Abstract] [Full Text] [Related]

  • 3. Aquaporin 4 deficiency modulates morphine pharmacological actions.
    Wu N, Lu XQ, Yan HT, Su RB, Wang JF, Liu Y, Hu G, Li J.
    Neurosci Lett; 2008 Dec 26; 448(2):221-5. PubMed ID: 18973795
    [Abstract] [Full Text] [Related]

  • 4. Spinal antinociception of synthetic omega-conotoxin SO-3, a selective N-type neuronal voltage-sensitive calcium channel blocker, and its effects on morphine analgesia in chemical stimulus tests in rodent.
    Yan LD, Liu YL, Zhang L, Dong HJ, Zhou PL, Su RB, Gong ZH, Huang PT.
    Eur J Pharmacol; 2010 Jun 25; 636(1-3):73-81. PubMed ID: 20361956
    [Abstract] [Full Text] [Related]

  • 5. Analgesic activity and pharmacological characterization of N-[1-phenylpyrazol-3-yl]-N-[1-(2-phenethyl)-4-piperidyl] propenamide, a new opioid agonist acting peripherally.
    Goicoechea C, Sánchez E, Cano C, Jagerovic N, Martín MI.
    Eur J Pharmacol; 2008 Oct 24; 595(1-3):22-9. PubMed ID: 18706410
    [Abstract] [Full Text] [Related]

  • 6. Synergistic antinociception between ZC88, an N-type voltage-dependent calcium channel blocker, and ibuprofen in mouse models of visceral and somatic inflammatory pain.
    Zhou WZ, Zhao TY, Wang ZY, Lu GY, Zhang SZ, Zhang C, Wu N, Li J.
    Eur J Pain; 2019 Jan 24; 23(1):46-56. PubMed ID: 29978517
    [Abstract] [Full Text] [Related]

  • 7. Anti-allodynic interactions between NMDA receptor channel blockers and morphine or clonidine in neuropathic rats.
    Malyshkin AA, Medvedev IO, Danysz W, Bespalov AY.
    Eur J Pharmacol; 2005 Sep 05; 519(1-2):80-5. PubMed ID: 16109402
    [Abstract] [Full Text] [Related]

  • 8. Molecular mechanisms in dizocilpine-induced attenuation of development of morphine dependence: an association with cortical Ca2+/calmodulin-dependent signal cascade.
    Hamdy MM, Noda Y, Miyazaki M, Mamiya T, Nozaki A, Nitta A, Sayed M, Assi AA, Gomaa A, Nabeshima T.
    Behav Brain Res; 2004 Jul 09; 152(2):263-70. PubMed ID: 15196794
    [Abstract] [Full Text] [Related]

  • 9. LPK-26, a novel kappa-opioid receptor agonist with potent antinociceptive effects and low dependence potential.
    Tao YM, Li QL, Zhang CF, Xu XJ, Chen J, Ju YW, Chi ZQ, Long YQ, Liu JG.
    Eur J Pharmacol; 2008 Apr 28; 584(2-3):306-11. PubMed ID: 18353307
    [Abstract] [Full Text] [Related]

  • 10. Blocking the R-type (Cav2.3) Ca2+ channel enhanced morphine analgesia and reduced morphine tolerance.
    Yokoyama K, Kurihara T, Saegusa H, Zong S, Makita K, Tanabe T.
    Eur J Neurosci; 2004 Dec 28; 20(12):3516-9. PubMed ID: 15610184
    [Abstract] [Full Text] [Related]

  • 11. Attenuation of opioid analgesic tolerance in p75 neurotrophin receptor null mutant mice.
    Trang T, Koblic P, Kawaja M, Jhamandas K.
    Neurosci Lett; 2009 Feb 13; 451(1):69-73. PubMed ID: 19114089
    [Abstract] [Full Text] [Related]

  • 12. Ellagic acid enhances morphine analgesia and attenuates the development of morphine tolerance and dependence in mice.
    Mansouri MT, Naghizadeh B, Ghorbanzadeh B.
    Eur J Pharmacol; 2014 Oct 15; 741():272-80. PubMed ID: 25179576
    [Abstract] [Full Text] [Related]

  • 13. Evaluation of selective NK(1) receptor antagonist CI-1021 in animal models of inflammatory and neuropathic pain.
    Gonzalez MI, Field MJ, Hughes J, Singh L.
    J Pharmacol Exp Ther; 2000 Aug 15; 294(2):444-50. PubMed ID: 10900217
    [Abstract] [Full Text] [Related]

  • 14. Interactions of intrathecally administered ziconotide, a selective blocker of neuronal N-type voltage-sensitive calcium channels, with morphine on nociception in rats.
    Wang YX, Gao D, Pettus M, Phillips C, Bowersox SS.
    Pain; 2000 Feb 15; 84(2-3):271-81. PubMed ID: 10666532
    [Abstract] [Full Text] [Related]

  • 15. On the mechanism of cross-tolerance between morphine- and nicotine-induced antinociception: involvement of calcium channels.
    Biala G, Weglinska B.
    Prog Neuropsychopharmacol Biol Psychiatry; 2006 Jan 15; 30(1):15-21. PubMed ID: 16202496
    [Abstract] [Full Text] [Related]

  • 16. Attenuation of morphine tolerance by minocycline and pentoxifylline in naive and neuropathic mice.
    Mika J, Wawrzczak-Bargiela A, Osikowicz M, Makuch W, Przewlocka B.
    Brain Behav Immun; 2009 Jan 15; 23(1):75-84. PubMed ID: 18684397
    [Abstract] [Full Text] [Related]

  • 17. 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 Jan 15; 135(1):247-61. PubMed ID: 16084657
    [Abstract] [Full Text] [Related]

  • 18. Modulation of oral morphine antinociceptive tolerance and naloxone-precipitated withdrawal signs by oral Delta 9-tetrahydrocannabinol.
    Cichewicz DL, Welch SP.
    J Pharmacol Exp Ther; 2003 Jun 15; 305(3):812-7. PubMed ID: 12606610
    [Abstract] [Full Text] [Related]

  • 19. Palmitic acid analogues exhibiting antinociceptive activity in mice.
    Déciga-Campos M, Montiel-Ruiz RM, Navarrete-Vázquez G, López-Muñoz FJ.
    Proc West Pharmacol Soc; 2007 Jun 15; 50():75-7. PubMed ID: 18605236
    [Abstract] [Full Text] [Related]

  • 20. [Analgesic effect of huwentoxin-I, a new N-type voltage-sensitive calcium channel blocker, on acute visceral pain in rats].
    Chen JQ, Chen WH, Deng MC, Li G, Kang Y, Ding ZH, Liang SP.
    Di Yi Jun Yi Da Xue Xue Bao; 2005 Jan 15; 25(1):10-4. PubMed ID: 15683987
    [Abstract] [Full Text] [Related]

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