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Journal Abstract Search

160 related items for PubMed ID: 33141426

  • 21. The FAAH inhibitor URB597 efficiently reduces tyrosine hydroxylase expression through CB₁- and FAAH-independent mechanisms.
    Bosier B, Muccioli GG, Lambert DM.
    Br J Pharmacol; 2013 Jun; 169(4):794-807. PubMed ID: 22970888
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  • 22. Analgesic effects of fatty acid amide hydrolase inhibition in a rat model of neuropathic pain.
    Jhaveri MD, Richardson D, Kendall DA, Barrett DA, Chapman V.
    J Neurosci; 2006 Dec 20; 26(51):13318-27. PubMed ID: 17182782
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  • 23. FAAH inhibition enhances anandamide mediated anti-tumorigenic effects in non-small cell lung cancer by downregulating the EGF/EGFR pathway.
    Ravi J, Sneh A, Shilo K, Nasser MW, Ganju RK.
    Oncotarget; 2014 May 15; 5(9):2475-86. PubMed ID: 24811863
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  • 24. Neuroprotective Effects of VEGF-A Nanofiber Membrane and FAAH Inhibitor URB597 Against Oxygen-Glucose Deprivation-Induced Ischemic Neuronal Injury.
    Wang DP, Jin KY, Zhao P, Lin Q, Kang K, Hai J.
    Int J Nanomedicine; 2021 May 15; 16():3661-3678. PubMed ID: 34093011
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  • 25. Monoacylglycerol Lipase Inhibition Prevents Short-Term Mitochondrial Dysfunction and Oxidative Damage in Rat Brain Synaptosomal/Mitochondrial Fractions and Cortical Slices: Role of Cannabinoid Receptors.
    Paredes-Ruiz KJ, Chavira-Ramos K, Galvan-Arzate S, Rangel-López E, Karasu Ç, Túnez I, Skalny AV, Ke T, Aschner M, Orozco-Morales M, Colín-González AL, Santamaría A.
    Neurotox Res; 2023 Dec 15; 41(6):514-525. PubMed ID: 37458923
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  • 27. Long-term administration of fatty acid amide hydrolase inhibitor (URB597) to rats with spontaneous hypertension disturbs liver redox balance and phospholipid metabolism.
    Biernacki M, Ambrożewicz E, Gęgotek A, Toczek M, Skrzydlewska E.
    Adv Med Sci; 2019 Mar 15; 64(1):15-23. PubMed ID: 30243113
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  • 28. Effect of Fatty Acid Amide Hydrolase Inhibitor URB597 on Orofacial Pain Perception in Rats.
    Zubrzycki M, Zubrzycka M, Wysiadecki G, Szemraj J, Jerczynska H, Stasiolek M.
    Int J Mol Sci; 2022 Apr 23; 23(9):. PubMed ID: 35563056
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  • 31. Elevation of endogenous anandamide impairs LTP, learning, and memory through CB1 receptor signaling in mice.
    Basavarajappa BS, Nagre NN, Xie S, Subbanna S.
    Hippocampus; 2014 Jul 23; 24(7):808-18. PubMed ID: 24648181
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  • 33. The fatty acid amide hydrolase inhibitor URB597 (cyclohexylcarbamic acid 3'-carbamoylbiphenyl-3-yl ester) reduces neuropathic pain after oral administration in mice.
    Russo R, Loverme J, La Rana G, Compton TR, Parrott J, Duranti A, Tontini A, Mor M, Tarzia G, Calignano A, Piomelli D.
    J Pharmacol Exp Ther; 2007 Jul 23; 322(1):236-42. PubMed ID: 17412883
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  • 36. 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 23; 72():116-25. PubMed ID: 23643752
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  • 37. Inhibitors of monoacylglycerol lipase, fatty-acid amide hydrolase and endocannabinoid transport differentially suppress capsaicin-induced behavioral sensitization through peripheral endocannabinoid mechanisms.
    Spradley JM, Guindon J, Hohmann AG.
    Pharmacol Res; 2010 Sep 23; 62(3):249-58. PubMed ID: 20416378
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  • 39. Effects of URB597 as an inhibitor of fatty acid amide hydrolase on modulation of nociception in a rat model of cholestasis.
    Hasanein P, Shahidi S, Komaki A, Mirazi N.
    Eur J Pharmacol; 2008 Sep 04; 591(1-3):132-5. PubMed ID: 18593578
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