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Journal Abstract Search

368 related items for PubMed ID: 18534634

  • 21. Rapid broad-spectrum analgesia through activation of peroxisome proliferator-activated receptor-alpha.
    LoVerme J, Russo R, La Rana G, Fu J, Farthing J, Mattace-Raso G, Meli R, Hohmann A, Calignano A, Piomelli D.
    J Pharmacol Exp Ther; 2006 Dec; 319(3):1051-61. PubMed ID: 16997973
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  • 22. Antinociceptive effects of meptazinol and its isomers on carrageenan-induced thermal hyperalgesia in rats.
    Wang PF, Zhang YQ, Qiu ZB, Zhao ZQ.
    Sheng Li Xue Bao; 2004 Jun 25; 56(3):295-300. PubMed ID: 15224140
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  • 23. Fatty acid amide hydrolase (FAAH) inhibition reduces L-3,4-dihydroxyphenylalanine-induced hyperactivity in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-lesioned non-human primate model of Parkinson's disease.
    Johnston TH, Huot P, Fox SH, Wakefield JD, Sykes KA, Bartolini WP, Milne GT, Pearson JP, Brotchie JM.
    J Pharmacol Exp Ther; 2011 Feb 25; 336(2):423-30. PubMed ID: 20966038
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  • 24. Interference with acute nausea and anticipatory nausea in rats by fatty acid amide hydrolase (FAAH) inhibition through a PPARα and CB1 receptor mechanism, respectively: a double dissociation.
    Rock EM, Limebeer CL, Ward JM, Cohen A, Grove K, Niphakis MJ, Cravatt BF, Parker LA.
    Psychopharmacology (Berl); 2015 Oct 25; 232(20):3841-8. PubMed ID: 26297326
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  • 26. Study of the regulation of the endocannabinoid system in a virus model of multiple sclerosis reveals a therapeutic effect of palmitoylethanolamide.
    Loría F, Petrosino S, Mestre L, Spagnolo A, Correa F, Hernangómez M, Guaza C, Di Marzo V, Docagne F.
    Eur J Neurosci; 2008 Aug 25; 28(4):633-41. PubMed ID: 18657182
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  • 30. Cyclooxygenases 1 and 2 contribute to peroxynitrite-mediated inflammatory pain hypersensitivity.
    Ndengele MM, Cuzzocrea S, Esposito E, Mazzon E, Di Paola R, Matuschak GM, Salvemini D.
    FASEB J; 2008 Sep 25; 22(9):3154-64. PubMed ID: 18497304
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  • 31. Attenuation of persistent pain-related behavior by fatty acid amide hydrolase (FAAH) inhibitors in a rat model of HIV sensory neuropathy.
    Nasirinezhad F, Jergova S, Pearson JP, Sagen J.
    Neuropharmacology; 2015 Aug 25; 95():100-9. PubMed ID: 25486617
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  • 32. The fatty acid amide hydrolase inhibitor, URB597, promotes retinal ganglion cell neuroprotection in a rat model of optic nerve axotomy.
    Slusar JE, Cairns EA, Szczesniak AM, Bradshaw HB, Di Polo A, Kelly ME.
    Neuropharmacology; 2013 Sep 25; 72():116-25. PubMed ID: 23643752
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  • 33. Reducing endocannabinoid metabolism with the fatty acid amide hydrolase inhibitor, URB597, fails to modify reinstatement of morphine-induced conditioned floor preference and naloxone-precipitated morphine withdrawal-induced conditioned floor avoidance.
    McCallum AL, Limebeer CL, Parker LA.
    Pharmacol Biochem Behav; 2010 Oct 25; 96(4):496-500. PubMed ID: 20643159
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  • 36. Acute intracerebroventricular administration of palmitoylethanolamide, an endogenous peroxisome proliferator-activated receptor-alpha agonist, modulates carrageenan-induced paw edema in mice.
    D'Agostino G, La Rana G, Russo R, Sasso O, Iacono A, Esposito E, Raso GM, Cuzzocrea S, Lo Verme J, Piomelli D, Meli R, Calignano A.
    J Pharmacol Exp Ther; 2007 Sep 25; 322(3):1137-43. PubMed ID: 17565008
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  • 38. The peripheral antinociceptive effects of endomorphin-1 and kynurenic acid in the rat inflamed joint model.
    Mecs L, Tuboly G, Nagy E, Benedek G, Horvath G.
    Anesth Analg; 2009 Oct 25; 109(4):1297-304. PubMed ID: 19762760
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  • 39. The novel reversible fatty acid amide hydrolase inhibitor ST4070 increases endocannabinoid brain levels and counteracts neuropathic pain in different animal models.
    Caprioli A, Coccurello R, Rapino C, Di Serio S, Di Tommaso M, Vertechy M, Vacca V, Battista N, Pavone F, Maccarrone M, Borsini F.
    J Pharmacol Exp Ther; 2012 Jul 25; 342(1):188-95. PubMed ID: 22514334
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