Potentiation of endocannabinoids and other lipid amides prevents hyperalgesia and inflammation in a pre-clinical model of migraine
Targeting fatty acid amide hydrolase (FAAH) is a promising therapeutic strategy to combat certain forms of pain, including migraine headache. FAAH inhibitors, such as the O-biphenyl-3-yl carbamate URB597, have been shown to produce anti-hyperalgesic effects in animal models of migraine. The objectiv...
Main Authors: | Demartini, C. (Author), Francavilla, M. (Author), Greco, R. (Author), Piomelli, D. (Author), Realini, N. (Author), Reggiani, A. (Author), Scarpelli, R. (Author), Tassorelli, C. (Author), Zanaboni, A.M (Author) |
---|---|
Format: | Article |
Language: | English |
Published: |
BioMed Central Ltd
2022
|
Subjects: | |
Online Access: | View Fulltext in Publisher |
Similar Items
-
Endocannabinoid System and Migraine Pain: An Update
by: Rosaria Greco, et al.
Published: (2018-03-01) -
Characterization of the peripheral FAAH inhibitor, URB937, in animal models of acute and chronic migraine
by: Rosaria Greco, et al.
Published: (2021-01-01) -
The role of the transient receptor potential ankyrin type-1 (TRPA1) channel in migraine pain: evaluation in an animal model
by: Chiara Demartini, et al.
Published: (2017-09-01) -
Role of Connexin 43 in an Inflammatory Model for TMJ Hyperalgesia
by: Fabeeha Ahmed, et al.
Published: (2021-08-01) -
Fatty acid amide hydrolase mediated endocannabinoid signaling in an early land plant, Physcomitrella patens
by: Haq, MD, et al.
Published: (2019)