The Endogenous Cannabinoid System: A Budding Source of Targets for Treating Inflammatory and Neuropathic Pain-Reference-Cited by-同舟云学术

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The Endogenous Cannabinoid System: A Budding Source of Targets for Treating Inflammatory and Neuropathic Pain

Published:2017-08-31 Issue:1 Volume:43 Page:52-79
ISSN:0893-133X
Container-title:Neuropsychopharmacology
language:en
Short-container-title:Neuropsychopharmacol.

Author:

Donvito Giulia,Nass Sara R,Wilkerson Jenny L,Curry Zachary A,Schurman Lesley D,Kinsey Steven G,Lichtman Aron H

Publisher

Springer Science and Business Media LLC

Subject

Psychiatry and Mental health,Pharmacology

Link

http://www.nature.com/articles/npp2017204.pdf

Reference311 articles.

1. Adamson Barnes NS, Mitchell VA, Kazantzis NP, Vaughan CW (2016). Actions of the dual FAAH/MAGL inhibitor JZL195 in a murine neuropathic pain model. Br J Pharmacol 173: 77–87.

2. Agarwal N, Pacher P, Tegeder I, Amaya F, Constantin CE, Brenner GJ et al (2007). Cannabinoids mediate analgesia largely via peripheral type 1 cannabinoid receptors in nociceptors. Nat Neurosci 10: 870–879.

3. Ahn K, Johnson DS, Mileni M, Beidler D, Long JZ, McKinney MK et al (2009). Discovery and characterization of a highly selective FAAH inhibitor that reduces inflammatory pain. Chem Biol 16: 411–420.

4. Ahn K, Smith SE, Liimatta MB, Beidler D, Sadagopan N, Dudley DT et al (2011). Mechanistic and pharmacological characterization of PF-04457845: a highly potent and selective fatty acid amide hydrolase inhibitor that reduces inflammatory and noninflammatory pain. J Pharmacol Exp Ther 338: 114–124.

5. Aley KO, Reichling DB, Levine JD (1996). Vincristine hyperalgesia in the rat: a model of painful vincristine neuropathy in humans. Neuroscience 73: 259–265.

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