2019
DOI: 10.1007/s00403-019-01963-4
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Double blinded, vehicle controlled, crossover study on the efficacy of a topical endocannabinoid membrane transporter inhibitor in atopic Beagles

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Cited by 8 publications
(8 citation statements)
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“…Several studies have suggested that the antipruritic, lipostatic and anti-inflammatory effects of CBD-and PEA-containing products have therapeutic potential for inflammatory skin disorders such as atopic dermatitis and acne vulgaris. 2,3,[15][16][17][18][19][20][21] However, the findings extrapolated from our study can only support the tolerability of certain cannabinoid products among healthy participants with nondiseased skin.…”
Section: Discussionmentioning
confidence: 83%
See 1 more Smart Citation
“…Several studies have suggested that the antipruritic, lipostatic and anti-inflammatory effects of CBD-and PEA-containing products have therapeutic potential for inflammatory skin disorders such as atopic dermatitis and acne vulgaris. 2,3,[15][16][17][18][19][20][21] However, the findings extrapolated from our study can only support the tolerability of certain cannabinoid products among healthy participants with nondiseased skin.…”
Section: Discussionmentioning
confidence: 83%
“…The impact of topical cannabinoids on skin health and potential anti-inflammatory modulation of the immune system has become a focus of attention as insight into the pathological roles of endogenous cannabinoids has increased. [1][2][3] Although data from animal studies are promising, the safety and tolerability of topical cannabinoid-containing products remain largely unexplored in humans. 4 Cannabidiol (CBD) and hemp oils are extracted from the flowers and leaves of the Cannabis sativa (hemp) plant.…”
Section: Introductionmentioning
confidence: 99%
“…Beagles allergic to dust mites were tested for the influence of endocannabinoid membrane transporter inhibitor on pruritus and dermatitis. Increasing levels of endocannabinoids improved atopic dermatitis and caused pruritus to alleviate after dust mite provocation in the experimental group [ 65 ].…”
Section: Cannabinoids In Inflammatory Skin Diseasesmentioning
confidence: 99%
“…[130] Feasibility of this mode of action was shown in a canine model of AD: topical application of WOL067-531 reduced AD flares in dogs after allergen exposure with negligible penetration into the circulation. [130] In a murine model, WOL067-531 significantly delayed barrier repair and reduced SDS-induced inflammation. [128] In a mouse model of dermatitis, the N-acylethanolamine acid amidase (NAAA) inhibitor ARN077 was shown to suppress inflammation and pruritus.…”
Section: Endo C Annab Inoid Sys Tem (Ec S) Modul Ator Smentioning
confidence: 99%
“…WOL067‐531 inhibits endocannabinoid reuptake, with the aim of prolonging and elevating endocannabinoid concentrations outside of the cell and enhancing activation of cannabinoid receptors. [ 130 ] Feasibility of this mode of action was shown in a canine model of AD: topical application of WOL067‐531 reduced AD flares in dogs after allergen exposure with negligible penetration into the circulation. [ 130 ] In a murine model, WOL067‐531 significantly delayed barrier repair and reduced SDS‐induced inflammation.…”
Section: Endocannabinoid System (Ecs) Modulatorsmentioning
confidence: 99%