Analgesic Effects of Fatty Acid Amide Hydrolase Inhibition in a Rat Model of Neuropathic Pain

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Analgesic Effects of Fatty Acid Amide Hydrolase Inhibition in a Rat Model of Neuropathic Pain

Cannabinoid-based medicines have therapeutic potential for the treatment of pain. Augmentation of levels of endocannabinoids with inhibitors of fatty acid amide hydrolase (FAAH) is analgesic in models of acute and inflammatory pain states. The aim of this study was to determine whether local inhibit...

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Bibliographic Details
Main Authors:	Jhaveri, Maulik, Richardson, Denise, Kendall, David, Barrett, David, Chapman, Victoria
Format:	Article
Published:	2006
Subjects:	Key words: electrophysiology; endocannabinoid; spinal nerve ligation; URB597; CB1 receptor; opioid receptor
Online Access:	https://eprints.nottingham.ac.uk/449/

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