Derailed Ceramide Metabolism in Atopic Dermatitis (AD): A Causal Starting Point for a Personalized (Basic) Therapy.

amitriptyline antioxidants apoptosis atopic dermatitis ceramide de novo synthesis ceramide metabolism linoleic acid lysosome lysosomotropic compounds sphingolipid profile

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
15 Aug 2019
Historique:
received: 19 07 2019
revised: 08 08 2019
accepted: 09 08 2019
entrez: 25 8 2019
pubmed: 25 8 2019
medline: 22 1 2020
Statut: epublish

Résumé

Active rebuilding, stabilizing, and maintaining the lipid barrier of the skin is an encouraging disease management and care concept for dry skin, atopic dermatitis (eczema, neurodermatitis), and psoriasis. For decades, corticosteroids have been the mainstay of topical therapy for atopic dermatitis; however, innovations within the scope of basic therapy are rare. In (extremely) dry, irritated, or inflammatory skin, as well as in lesions, an altered (sphingo)lipid profile is present. Recovery of a balanced (sphingo)lipid profile is a promising target for topical and personalized treatment and prophylaxis. New approaches for adults and small children are still lacking. With an ingenious combination of commonly used active ingredients, it is possible to restore and reinforce the dermal lipid barrier and maintain refractivity. Lysosomes and ceramide de novo synthesis play a key role in attenuation of the dermal lipid barrier. Linoleic acid in combination with amitriptyline in topical medication offers the possibility to relieve patients affected by dry and itchy skin, mild to moderate atopic dermatitis lesions, and eczemas without the commonly occurring serious adverse effects of topical corticosteroids or systemic antibody administration.

Identifiants

pubmed: 31443157
pii: ijms20163967
doi: 10.3390/ijms20163967
pmc: PMC6720956
pii:
doi:

Substances chimiques

Antioxidants 0
Ceramides 0
Sphingolipids 0
Amitriptyline 1806D8D52K
Linoleic Acid 9KJL21T0QJ

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Markus Blaess (M)

Institute of Precision Medicine, Medical and Life Sciences Faculty, Furtwangen University, Jakob-Kienzle-Strasse 17, 78054 Villingen-Schwenningen, Germany.

Hans-Peter Deigner (HP)

Institute of Precision Medicine, Medical and Life Sciences Faculty, Furtwangen University, Jakob-Kienzle-Strasse 17, 78054 Villingen-Schwenningen, Germany. Hans-Peter.Deigner@hs-furtwangen.de.
EXIM Department, Fraunhofer Institute IZI Leipzig, Schillingallee 68, 18057 Rostock, Germany. Hans-Peter.Deigner@hs-furtwangen.de.

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Classifications MeSH