The effects of a novel synthetic retinoid, seletinoid G, on the expression of extracellular matrix proteins in aged human skin in vivo

Clin Chim Acta. 2005 Dec;362(1-2):161-9. doi: 10.1016/j.cccn.2005.06.016. Epub 2005 Aug 1.

Abstract

Background: Although retinoids have potential efficacy in aged skin, their side effect (skin irritation) remains a clinical problem. We designed a novel synthetic retinoid, seletinoid G, by using computer-aided molecular modeling, and investigated its effects on the expression of extracellular matrix proteins in human skin in vivo.

Methods: Twenty-three subjects were tested on the buttocks using 4-day occlusive application of seletinoid G and all-trans retinoic acid (tRA). Skin irritation after topical application was quantified by the degree of erythema and cutaneous blood flow. The expression of extracellular matrix proteins and interstitial collagenase (MMP-1) in skin biopsies was investigated by immunohistochemical staining and Western blotting.

Results: The topical application of seletinoid G under occlusion induced no skin irritation in contrast to tRA, which caused severe erythema. The topical treatment with seletinoid G increased the expressions of type I procollagen, tropoelastin, and fibrillin-1, and reduced MMP-1 in old skin in vivo. Seletinoid G was found to inhibit not only the UV-induced decrease of type I procollagen but the UV-induced increase of MMP-1 and c-Jun protein in young skin in vivo.

Conclusions: Seletinoid G is a novel synthetic retinoid, which has little the side effect of skin irritation after topical application. Seletinoid G can repair altered connective tissue in old skin and inhibit UV-induced collagen deficiency in young skin.

Publication types

  • Clinical Trial

MeSH terms

  • Adult
  • Aged
  • Dioxolanes / chemical synthesis*
  • Dioxolanes / chemistry
  • Dioxolanes / pharmacology*
  • Extracellular Matrix Proteins / metabolism*
  • Female
  • Gene Expression Regulation / drug effects*
  • Humans
  • Male
  • Matrix Metalloproteinase 1 / metabolism
  • Molecular Structure
  • Proto-Oncogene Proteins c-jun / metabolism
  • Pyrans / chemical synthesis*
  • Pyrans / chemistry
  • Pyrans / pharmacology*
  • Retinoids / chemical synthesis*
  • Retinoids / chemistry
  • Retinoids / pharmacology*
  • Skin Aging / drug effects*
  • Skin Aging / radiation effects
  • Tretinoin / pharmacology

Substances

  • Dioxolanes
  • Extracellular Matrix Proteins
  • Proto-Oncogene Proteins c-jun
  • Pyrans
  • Retinoids
  • seletinoid G
  • Tretinoin
  • Matrix Metalloproteinase 1