Identification of potential anti-photoageing algal compounds using an in-vitro model of photoageing

J Pharm Pharmacol. 2006 Dec;58(12):1577-83. doi: 10.1211/jpp.58.12.0003.

Abstract

Stress-induced premature senescence (SIPS) has been proposed as an in-vitro model for testing the long-term effects of stressful events and to find molecules/natural extracts that protect against such stress. Premature senescence of human skin diploid fibroblasts (HDFs) can be induced by repeated subcytotoxic exposure to UVB, with the appearance of so-called biomarkers of senescence such as growth arrest, senescence-associated beta-galactosidase activity, senescence-associated gene over-expression and the common 4977-bp mitochondrial DNA deletion. This model of UVB-induced premature senescence has been acknowledged as a robust in-vitro model in photoageing research. In this study, the potential anti-photoageing effects of a series of algal extracts were tested. The appearance of the biomarkers of UVB-induced premature senescence of HDFs was studied with or without algal extracts. One algal extract was shown to be particularly protective against UVB-induced SIPS. The results obtained here reinforce the notion that UVB-induced premature senescence of HDFs can be used to screen potential anti-photoageing compounds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Survival / drug effects
  • Cell Survival / physiology
  • Cell Survival / radiation effects
  • Cells, Cultured
  • Cellular Senescence / drug effects*
  • Cellular Senescence / physiology
  • Cellular Senescence / radiation effects
  • Clusterin / genetics
  • Clusterin / metabolism
  • DNA, Mitochondrial / genetics
  • Dermatitis, Phototoxic / prevention & control
  • Eukaryota / chemistry*
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism
  • Fibroblasts / radiation effects
  • Fibronectins / genetics
  • Fibronectins / metabolism
  • Gene Expression / drug effects
  • Humans
  • Mitosis / drug effects
  • Mitosis / physiology
  • Mitosis / radiation effects
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Skin Aging / drug effects
  • Skin Aging / physiology
  • Skin Aging / radiation effects
  • Sunscreening Agents / chemistry
  • Sunscreening Agents / isolation & purification
  • Sunscreening Agents / pharmacology*
  • Thymidine / metabolism
  • Tritium
  • Ultraviolet Rays
  • beta-Galactosidase / metabolism

Substances

  • Clusterin
  • DNA, Mitochondrial
  • Fibronectins
  • RNA, Messenger
  • Sunscreening Agents
  • Tritium
  • beta-Galactosidase
  • Thymidine