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The anti‐inflammatory mediator palmitoylethanolamide enhances the levels of 2‐arachidonoyl‐glycerol and potentiates its actions at TRPV1 cation channels

BACKGROUND AND PURPOSE: Palmitoylethanolamide (PEA) is an endogenous congener of anandamide and potentiates its actions at cannabinoid CB (1) and CB (2) receptors, and at transient receptor potential vanilloid type‐1 (TRPV1) channels. The other endocannabinoid, 2‐arachidonoylglycerol (2‐AG), was rec...

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Detaylı Bibliyografya
Yayımlandı:Br J Pharmacol
Asıl Yazarlar: Petrosino, Stefania, Schiano Moriello, Aniello, Cerrato, Santiago, Fusco, Mariella, Puigdemont, Anna, De Petrocellis, Luciano, Di Marzo, Vincenzo
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2015
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5338153/
https://ncbi.nlm.nih.gov/pubmed/25598150
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bph.13084
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