Palmitoylethanolamide, a naturally occurring lipid, is an orally effective intestinal anti-inflammatory agent

Palmitoylethanolamide (PEA, PeaPure) is an effective natural intestinal anti-inflammatory.

Background and Purpose

Palmitoylethanolamide (PEA) acts via several targets, including cannabinoid CB₁ and CB₂ receptors, transient receptor potential vanilloid type-1 (TRPV1) ion channels, peroxisome proliferator-activated receptor alpha (PPAR α) and orphan G protein-coupled receptor 55 (GRR55), all involved in the control of intestinal inflammation. Here, we investigated the effect of PEA in a murine model of colitis.

Experimental Approach

Colitis was induced in mice by intracolonic administration of dinitrobenzenesulfonic acid (DNBS). Inflammation was assessed by evaluating inflammatory markers/parameters and by histology; intestinal permeability by a fluorescent method; colonic cell proliferation by immunohistochemistry; PEA and endocannabinoid levels by liquid chromatography mass spectrometry; receptor and enzyme mRNA expression by quantitative RT-PCR.

Key Results

DNBS administration caused inflammatory damage, increased colonic levels of PEA and endocannabinoids, down-regulation of mRNA for TRPV1 and GPR55 but no changes in mRNA for CB₁, CB₂ and PPARα. Exogenous PEA (i.p. and/or p.o., 1 mg·kg⁻¹) attenuated inflammation and intestinal permeability, stimulated colonic cell proliferation, and increased colonic TRPV1 and CB₁ receptor expression. The anti-inflammatory effect of PEA was attenuated or abolished by CB₂ receptor, GPR55 or PPARα antagonists and further increased by the TRPV1 antagonist capsazepine.

Conclusions and Implications

PEA improves murine experimental colitis, the effect being mediated by CB₂ receptors, GPR55 and PPARα, and modulated by TRPV1 channels.

Source:

Borrelli, F., Romano, B., Petrosino, S., Pagano, E., Capasso, R., Coppola, D., Battista, G., Orlando, P., Di Marzo, V. and Izzo, A. A. (2015), Palmitoylethanolamide, a naturally occurring lipid, is an orally effective intestinal anti-inflammatory agent. British Journal of Pharmacology, 172: 142–158. doi: 10.1111/bph.12907
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