Protective effect of polypeptide from Chlamys farreri on mitochondria in human dermal fibroblasts irradiated by ultraviolet B

Acta Pharmacol Sin. 2003 Jul;24(7):692-6.

Abstract

Aim: To study the effect of polypeptide from Chlamys farreri (PCF) on mitochondria of human dermal fibroblasts irradiated by ultraviolet B (UVB) in vitro.

Methods: Malondialdehyde (MDA) and antioxidant enzymes including superoxide dismutase (SOD) and glutathione peroxidase (GSH-PX) were determined by biochemical methods. Mitochondrial transmembrane potential was measured by flow cytometry. Ultrastructure of fibroblasts was observed with transmission electron microscope.

Results: UVB (1.176 x 10(-4) J/cm(2)) induced mitochondria damage in dermal fibroblast and PCF (0.25%-1%) reduced the damage in a concentration-dependent manner. Furthermore, PCF also concentration-dependently maintained the stability of mitochondrial transmembrane potential. PCF was able to reduce the MDA formation caused by UVB, meanwhile increased the activities of SOD and GSH-PX. The differences among the PCF groups and UVB model group were significant (P<0.05, P<0.01).

Conclusion: The UVB-induced mitochondria damage was alleviated by PCF in human dermal fibroblasts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Animals
  • Antioxidants / pharmacology
  • Cells, Cultured
  • Dermis / cytology
  • Dose-Response Relationship, Drug
  • Fibroblasts / drug effects*
  • Fibroblasts / radiation effects
  • Fibroblasts / ultrastructure
  • Glutathione Peroxidase / metabolism
  • Humans
  • Malondialdehyde / metabolism
  • Materia Medica / isolation & purification
  • Materia Medica / pharmacology*
  • Membrane Potentials
  • Mitochondria / drug effects*
  • Mitochondria / physiology
  • Mitochondria / radiation effects
  • Mollusca / chemistry*
  • Peptides / isolation & purification
  • Peptides / pharmacology*
  • Superoxide Dismutase / metabolism
  • Ultraviolet Rays

Substances

  • Antioxidants
  • Materia Medica
  • Peptides
  • Malondialdehyde
  • Glutathione Peroxidase
  • Superoxide Dismutase