4.7 Article

Palmitoylethanolamide reduces inflammation and itch in a mouse model of contact allergic dermatitis

Journal

EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 791, Issue -, Pages 669-674

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejphar.2016.10.005

Keywords

Angiogenesis Contact allergic dermatitis (CAD); Dinitrofluorobenzene (DNFB); Itch; Mast cells (MCs); Palmitoylethanolamide (PEA)

Funding

  1. Progetto Operativo Nazionale [PON01_02512]
  2. [PO FESR 2007/20013]

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In mice, 2,4-dinitrofluorobenzene (DNFB) induces contact allergic dermatitis (CAD), which, in a late phase, is characterized by mast cell (MC) infiltration and angiogenesis. Palmitoylethanolamide (PEA), an endogenous anti-inflammatory molecule, acts by down-modulating MCs following activation of the cannabinoid CB2 receptor and peroxisome proliferator-activated receptor-alpha (PPAR-alpha). We have previously reported the anti-inflammatory effect of PEA in the early stage of CAD. Here, we examined whether PEA reduces the features of the late stage of CAD including MC activation, angiogenesis and itching. After sensitization to DNFB, female C57BL/6J mice underwent to three DNFB challenges at days 5, 12 and 19 and treatments were given at each challenge and for two more days. CAD was expressed as Delta increase in ear thickness between challenged and unchallenged mice. PEA (5 mg/kg/i.p.) reduced: i) the DNFB-induced Delta increase; ii) the number of MCs per tissue area; iii) the expression of VEGF and its receptor Flk-1. These effects were reversed by co-administration of AM630 (1 mg/kg/i.p.), a CB2 antagonist, but not GW6471 (1 mg/kg/i.p.), a PPAR-alpha antagonist. Finally, PEA reduced the number of ear scratchings 48 h after DNFB challenge and this effect was reversed by both CB2 and PPAR-alpha antagonists, suggesting the involvement of both receptors. PEA, by reducing the features of late stage CAD in mice, may be beneficial in this pathological condition.

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