Peer-reviewed veterinary case report
Ultramicronized palmitoylethanolamide reduces skin irritation in dogs
By Abramo, Francesca et al.·Published in Veterinary dermatology·2017·Department of Veterinary Sciences, Italy·View original on PubMed →
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Original publication title: Ultramicronized palmitoylethanolamide counteracts the effects of compound 48/80 in a canine skin organ culture model.
- Species:
- dog
Plain-English summary
A study found that ultramicronized palmitoylethanolamide (PEA-um) can help reduce skin problems in dogs with allergies. In tests using skin samples from healthy dogs, PEA-um significantly decreased the activity of mast cells, which are involved in allergic reactions, and reduced the release of histamine, a chemical that causes itching and inflammation. This suggests that PEA-um could be a beneficial treatment for dogs suffering from conditions like atopic dermatitis, helping to soothe their skin and lessen allergic reactions.
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Abstract
BACKGROUND: Ultramicronized palmitoylethanolamide (PEA-um) has been reported to reduce pruritus and skin lesions in dogs with moderate atopic dermatitis and pruritus. HYPOTHESIS/OBJECTIVES: A canine ex vivo skin model was used to investigate the ability of PEA-um to counteract changes induced by compound 48/80, a well-known secretagogue that causes mast cell degranulation. ANIMALS: Normal skin was obtained from three donor dogs subjected to surgery for reasons unrelated to the study. METHODS: Cultured skin biopsy samples in triplicate were treated with 10 and 100 μg/mL compound 48/80, without or with 30 μM PEA-um. Mast cell (MC) degranulation, histamine release into the culture medium, local microvascular dilatation, epidermal thickness, keratinocyte proliferation and epidermal differentiation markers were evaluated. RESULTS: Exposure of the skin organ culture to PEA-um 24 h before and 72 h concomitantly to compound 48/80 resulted in a significant decrease of degranulating MCs. PEA-um also reduced the histamine content in the culture medium by half, although the effect did not reach statistical significance. PEA-um significantly counteracted vasodilation induced by 100 μg/mL compound 48/80. Finally, PEA-um alone did not induce changes in epidermal thickness, differentiation markers, keratinocyte proliferation, MC density and/or degranulation. CONCLUSIONS AND CLINICAL IMPORTANCE: Collectively, these results support the protective action PEA-um on the skin of dogs undergoing allergic changes.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/28585337/