Details

Autor(en) / Beteiligte

• Maubec, Eve
• Laouénan, Cédric
• Deschamps, Lydia
• Nguyen, Van Tuan
• Scheer-Senyarich, Isabelle
• Wackenheim-Jacobs, Anne-Catherine
• Steff, Maud
• Duhamel, Stéphanie
• Tubiana, Sarah
• Brahimi, Nesrine
• Leclerc-Mercier, Stéphanie
• Crickx, Béatrice
• Perret, Claudine
• Aractingi, Selim
• Escoubet, Brigitte
• Duval, Xavier
• Arnaud, Philippe
• Jaisser, Frederic
• Mentré, France
• Farman, Nicolette

Titel

Topical Mineralocorticoid Receptor Blockade Limits Glucocorticoid-Induced Epidermal Atrophy in Human Skin

Ist Teil von

• Journal of investigative dermatology, 2015-07, Vol.135 (7), p.1781-1789

Ort / Verlag

United States: Elsevier Inc

Erscheinungsjahr

2015

Link zum Volltext

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• A major deleterious side effect of glucocorticoids is skin atrophy. Glucocorticoids activate the glucocorticoid and the mineralocorticoid (MR) receptor, both present in the epidermis. We hypothesized that glucocorticoid-induced epidermal atrophy may be related to inappropriate occupancy of MR by glucocorticoids. We evaluated whether epidermal atrophy induced by the topical glucocorticoid clobetasol could be limited by coadministration of MR antagonist. In cultured human skin explants, the epidermal atrophy induced by clobetasol was significantly limited by MR antagonism (canrenoate and eplerenone). Blockade of the epithelial sodium channel ENaC by phenamil was also efficient, identifying a role of MR–ENaC cascade in keratinocytes, acting through restoration of clobetasol-induced impairment of keratinocyte proliferation. In the SPIREPI randomized double-blind controlled trial, gels containing clobetasol, the MR antagonist spironolactone, both agents, or placebo were applied on four zones of the forearms of 23 healthy volunteers for 28 days. Primary outcome was histological thickness of the epidermis with clobetasol alone or clobetasol+spironolactone. Spironolactone alone did not affect the epidermal thickness but coapplication of clobetasol and spironolactone significantly limited clobetasol-induced atrophy and was well tolerated. Altogether, these findings identify MR as a factor regulating epidermal homeostasis and suggest that topical MR blockade could limit glucocorticoid-induced epidermal atrophy.