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National Institute of Environmental Health Sciences

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Publication Detail

Title: Effects of palmitoylethanolamide on aqueous humor outflow.

Authors: Kumar, Akhilesh; Qiao, Zhuanhong; Kumar, Pritesh; Song, Zhao-Hui

Published In Invest Ophthalmol Vis Sci, (2012 Jul 03)

Abstract: To study the effects of palmitoylethanolamide (PEA), a fatty acid ethanolamide, on aqueous humor outflow facility.The effects of PEA on outflow facility were measured using a porcine anterior segment-perfused organ culture model. The involvements of different receptors in PEA-induced changes were investigated using receptor antagonists and adenovirus delivered small hairpin RNAs (shRNAs). PEA-induced activation of p42/44 mitogen-activated protein kinase (MAPK) was determined by Western blot analysis using an antiphospho p42/44 MAPK antibody.PEA caused a concentration-dependent enhancement of outflow facility, with the maximum effect (151.08 ± 11.12% of basal outflow facility) achieved at 30 nM of PEA. Pretreatment of anterior segments with 1 μM cannabinoid receptor 2 antagonist SR144528 and 1 μM PPARα antagonist GW6471, but not 1 μM cannabinoid receptor 1 antagonist SR141716A, produced a partial antagonism on the PEA-induced increase of outflow facility. Treatment of TM cells with PEA for 10 minutes activated phosphorylation of p42/44 MAPK, which was blocked by pretreatment with SR1444528 and GW6471, but not SR141716A. Knocking down the expression of either GPR55 or PPARα receptors with specific shRNAs for these receptors partially blocked PEA-induced increase in outflow facility and abolished PEA-induced phosphorylation of p42/44 MAPK. PD98059, an inhibitor of the p42/44 MAPK pathway, blocked both PEA-induced enhancement of aqueous humor outflow facility and PEA-induced phosphorylation of p42/44 MAPK.Our results demonstrate that PEA increases aqueous humor outflow through the TM pathway and these effects are mediated by GPR55 and PPARα receptors through activation of p42/44 MAPK.

PubMed ID: 22589443 Exiting the NIEHS site

MeSH Terms: Animals; Aqueous Humor/secretion*; Blotting, Western; Bornanes/pharmacology; Dose-Response Relationship, Drug; Endocannabinoids; Enzyme Activation; Ethanolamines; Humans; Mitogen-Activated Protein Kinase 1/metabolism; Mitogen-Activated Protein Kinase 3/metabolism; Organ Culture Techniques; Oxazoles/pharmacology; PPAR alpha/antagonists & inhibitors; PPAR alpha/metabolism; Palmitic Acids/antagonists & inhibitors; Palmitic Acids/pharmacology*; Phosphorylation; Piperidines/pharmacology; Pyrazoles/pharmacology; Receptor, Cannabinoid, CB1/antagonists & inhibitors; Receptor, Cannabinoid, CB2/antagonists & inhibitors; Receptors, G-Protein-Coupled/metabolism; Swine; Trabecular Meshwork/drug effects*; Trabecular Meshwork/metabolism; Tyrosine/analogs & derivatives; Tyrosine/pharmacology

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