Antinociceptive effects of tetrazole inhibitors of endocannabinoid inactivation: cannabinoid and non-cannabinoid receptor-mediated mechanisms

BACKGROUND AND PURPOSE: Tetrazoles were recently developed as inhibitors of the cellular uptake of the endocannabinoid anandamide or of its hydrolysis by fatty acid amide hydrolase (FAAH), but were proposed to act also on non-endocannabinoid-related serine hydrolases. EXPERIMENTAL APPROACH: We teste...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Maione, S, Morera, E, Marabese, I, Ligresti, A, Luongo, L, Ortar, G, Di Marzo, V
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Nature Publishing Group 2008
Aiheet:
Research Papers
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2584918/
https://ncbi.nlm.nih.gov/pubmed/18660824
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/bjp.2008.308
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