volume 306 issue 8 pages 719-729

Calcipotriol counteracts betamethasone-induced decrease in extracellular matrix components related to skin atrophy

Hanne Norsgaard 1
Sandrine Kurdykowski 2
Pascal Descargues 2
Tatiana Gonzalez 3
Troels Marstrand 1
Georg Dünstl 4
Mads Røpke 5
1
 
Department of Molecular Biomedicine, LEO Pharma A/S, Ballerup, Denmark
2
 
Genoskin, Oncopole, Toulouse, France
3
 
Disease Pharmacology, LEO Pharma A/S, Ballerup, Denmark
4
 
External Discovery, LEO Pharma A/S, Ballerup, Denmark
5
 
Clinical Pharmacology, LEO Pharma A/S, Ballerup, Denmark
Publication typeJournal Article
Publication date2014-07-16
scimago Q1
wos Q3
SJR0.879
CiteScore3.3
Impact factor2.1
ISSN03403696, 1432069X
General Medicine
Dermatology
Abstract
The calcipotriol/betamethasone dipropionate fixed-combination gel is widely used for topical treatment of psoriasis vulgaris. It has been hypothesized that calcipotriol counteracts glucocorticoid-induced skin atrophy which is associated with changes in the extracellular matrix (ECM). To elucidate the combined effects of calcipotriol and betamethasone on key ECM components, a comparative study to the respective mono-treatments was carried out. The effect on collagen I synthesis, matrix metalloproteinase (MMP) secretion, and hyaluronic acid (HA) production was investigated in primary human fibroblast and keratinocyte cultures as well as in a human skin explant model. We show that calcipotriol counteracts betamethasone-induced suppression of collagen I synthesis. Similarly, calcipotriol and betamethasone have opposing effects on MMP expression in both fibroblasts and keratinocytes. Moreover, calcipotriol is able to restore betamethasone-impaired HA synthesis in keratinocytes and prevent betamethasone-induced epidermal thinning in minipigs upon treatment with the calcipotriol/betamethasone gel. In summary, our results show for the first time in primary human skin cultures that calcipotriol reduces early signs of betamethasone-induced skin atrophy by modulation of key ECM components. These results indicate that the calcipotriol component of the fixed-combination gel counteracts the atrophogenic effects of betamethasone on the skin.
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GOST Copy
Norsgaard H. et al. Calcipotriol counteracts betamethasone-induced decrease in extracellular matrix components related to skin atrophy // Archives of Dermatological Research. 2014. Vol. 306. No. 8. pp. 719-729.
GOST all authors (up to 50) Copy
Norsgaard H., Kurdykowski S., Descargues P., Gonzalez T., Marstrand T., Dünstl G., Røpke M. Calcipotriol counteracts betamethasone-induced decrease in extracellular matrix components related to skin atrophy // Archives of Dermatological Research. 2014. Vol. 306. No. 8. pp. 719-729.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1007/s00403-014-1485-3
UR - https://doi.org/10.1007/s00403-014-1485-3
TI - Calcipotriol counteracts betamethasone-induced decrease in extracellular matrix components related to skin atrophy
T2 - Archives of Dermatological Research
AU - Norsgaard, Hanne
AU - Kurdykowski, Sandrine
AU - Descargues, Pascal
AU - Gonzalez, Tatiana
AU - Marstrand, Troels
AU - Dünstl, Georg
AU - Røpke, Mads
PY - 2014
DA - 2014/07/16
PB - Springer Nature
SP - 719-729
IS - 8
VL - 306
PMID - 25027750
SN - 0340-3696
SN - 1432-069X
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2014_Norsgaard,
author = {Hanne Norsgaard and Sandrine Kurdykowski and Pascal Descargues and Tatiana Gonzalez and Troels Marstrand and Georg Dünstl and Mads Røpke},
title = {Calcipotriol counteracts betamethasone-induced decrease in extracellular matrix components related to skin atrophy},
journal = {Archives of Dermatological Research},
year = {2014},
volume = {306},
publisher = {Springer Nature},
month = {jul},
url = {https://doi.org/10.1007/s00403-014-1485-3},
number = {8},
pages = {719--729},
doi = {10.1007/s00403-014-1485-3}
}
MLA
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MLA Copy
Norsgaard, Hanne, et al. “Calcipotriol counteracts betamethasone-induced decrease in extracellular matrix components related to skin atrophy.” Archives of Dermatological Research, vol. 306, no. 8, Jul. 2014, pp. 719-729. https://doi.org/10.1007/s00403-014-1485-3.