Dexpanthenol enhances skin barrier repair and reduces inflammation after sodium lauryl sulphate-induced irritation

被引:74
作者
Proksch, E
Nissen, HP
机构
[1] Univ Kiel, Dept Dermatol, D-24105 Kiel, Germany
[2] Dermaconsult, Bonn, Germany
关键词
inflammation; pantothenic acid; skin hydration; sodium lauryl/dodecyl sulphate; transcutaneous/transepidermal water loss; wound healing;
D O I
10.1080/09546630212345674
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
BACKGROUND: Dexpanthenol-containing creams have been widely used for treatment of lesions (superficial wounds) of the skin and mucous membranes. Dexpanthenol is converted in tissues to pantothenic acid, a component of coenzyme A. Coenzyme A catalyses early steps in the synthesis of fatty acids and sphingolipids which are of crucial importance for stratum corneum lipid bilayers and cell membrane integrity. AIM: In the present study, the effects were examined of a dexpanthenol-containing cream on skin barrier repair, stratum corneum hydration, skin roughness, and inflammation after sodium lauryl sulphate (SLS)induced irritation. METHODS: Irritation was induced by application of SLS in patch test chambers. The dexpanthenol-containing cream or the vehicle were applied twice daily and barrier repair, hydration, roughness, and inflammation of the skin were determined by using biophysical methods. RESULTS: Significantly accelerated skin barrier repair was found in treatments with the dexpanthenol-containing cream (verum) compared with vehicle-treated (placebo) or untreated skin. Both verum and placebo showed an increase in stratum corneum hydration, but significantly more so with the dexpanthenol-containing cream. Both creams reduced skin roughness, but again the verum was superior. The dexpanthenol-containing cream significantly reduced skin redness as a sign of inflammation in contrast to the vehicle, which produced no effect. CONCLUSION: Treatment with a dexpanthenol-containing cream showed significantly enhanced skin barrier repair and stratum corneum hydration, while reducing skin roughness and inflammation.
引用
收藏
页码:173 / 178
页数:6
相关论文
共 33 条
[1]   ENZYMATIC CONVERSION OF PANTOTHENYLA6COHOL TO PANTOTHENIC ACID [J].
ABIKO, Y ;
TOMIKAWA, M ;
SHIMIZU, M .
JOURNAL OF VITAMINOLOGY, 1969, 15 (01) :59-&
[2]  
BORELLI S, 1974, INFORMIERTE ARZT, V2, P509
[3]  
BUDDECKE E, 1997, GRUNDRISS BIOCH, P40
[4]   Cytokines and irritant contact dermatitis [J].
Corsini, E ;
Galli, CL .
TOXICOLOGY LETTERS, 1998, 103 :277-282
[5]   Stress alters cutaneous permeability barrier homeostasis [J].
Denda, M ;
Tsuchiya, T ;
Elias, PM ;
Feingold, KR .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2000, 278 (02) :R367-R372
[6]   Expression of epidermal keratins and the cornified envelope protein involucrin is influenced by permeability barrier disruption [J].
Ekanayake-Mudiyanselage, S ;
Aschauer, H ;
Schmook, FP ;
Jensen, JM ;
Meingassner, JG ;
Proksch, E .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1998, 111 (03) :517-523
[7]   MAMMALIAN EPIDERMAL BARRIER LAYER LIPIDS - COMPOSITION AND INFLUENCE ON STRUCTURE [J].
ELIAS, PM ;
GOERKE, J ;
FRIEND, DS .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1977, 69 (06) :535-546
[8]  
Fartasch M, 1998, J Investig Dermatol Symp Proc, V3, P121
[9]   Guidelines for measurement of skin colour and erythema - A report from the standardization group of the European society of contact dermatitis [J].
Fullerton, A ;
Fischer, T ;
Lahti, A ;
Wilhelm, KP ;
Takiwaki, H ;
Serup, J .
CONTACT DERMATITIS, 1996, 35 (01) :1-10
[10]  
Gehring W, 2000, ARZNEIMITTEL-FORSCH, V50, P659