Inhibition effect of Gynura procumbens extract on UV-B-induced matrix-metalloproteinase expression in human dermal fibroblasts

J Ethnopharmacol. 2011 Sep 1;137(1):427-33. doi: 10.1016/j.jep.2011.04.072. Epub 2011 Jun 6.

Abstract

Ethnopharmacological relevance: Gynura procumbens Merr. (Asteraceae) has been used as a traditional remedy for various skin diseases in certain areas of Southeast Asia.

Aim of the study: In order to evaluate the protective activity of Gynura procumbens extract on skin photoaging and elucidate its mode of action.

Materials and methods: Matrix-metalloproteinase (MMP)-1 and -9 expressions were induced by UV-B irradiation in human primary dermal fibroblasts. MMP-1 expression level was measured by enzyme-linked immunosorbent assay (ELISA) and Western blot analysis. Zymography was employed for evaluating the enzymatic activity of MMP-9. Anti-inflammatory activity and anti-oxidative capacity of the extract were evaluated by ELISA and dichlorodihydrofluorescein diacetate (DCF-DA) assay.

Results: The ethanolic extract of Gynura procumbens inhibited MMP-1 expression up to 70% compare to negative control group. The enzymatic activity of MMP-9 was inhibited around 73% by the treatment of 20μg/mL of the extract. The extract markedly reduced the production of reactive oxygen species (ROS). Gynura procumbens extract showed an inhibitory effect on releasing pro-inflammatory cytokines (IL-6 and IL-8) in human HaCat keratinocyte.

Conclusion: The ethanolic extract of Gynura procumbens inhibited MMP-1 and MMP-9 expressions induced by UV-B irradiation via inhibition of pro-inflammatory cytokine mediator release and ROS production.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Inflammatory Agents / pharmacology
  • Antioxidants / pharmacology
  • Asteraceae* / chemistry
  • Blotting, Western
  • Cells, Cultured
  • Chromatography, High Pressure Liquid
  • Dermatologic Agents / chemistry
  • Dermatologic Agents / isolation & purification
  • Dermatologic Agents / pharmacology*
  • Dermis / drug effects*
  • Dermis / enzymology
  • Dermis / radiation effects
  • Dose-Response Relationship, Drug
  • Enzyme-Linked Immunosorbent Assay
  • Ethanol / chemistry
  • Fibroblasts / drug effects*
  • Fibroblasts / enzymology
  • Fibroblasts / radiation effects
  • Humans
  • Inflammation Mediators / metabolism
  • Interleukin-6 / metabolism
  • Interleukin-8 / metabolism
  • Matrix Metalloproteinase 1 / metabolism*
  • Matrix Metalloproteinase 9 / metabolism*
  • Plant Extracts / chemistry
  • Plant Extracts / isolation & purification
  • Plant Extracts / pharmacology*
  • Plant Leaves
  • Reactive Oxygen Species / metabolism
  • Skin Aging / drug effects*
  • Skin Aging / radiation effects
  • Solvents / chemistry
  • Ultraviolet Rays*

Substances

  • Anti-Inflammatory Agents
  • Antioxidants
  • CXCL8 protein, human
  • Dermatologic Agents
  • IL6 protein, human
  • Inflammation Mediators
  • Interleukin-6
  • Interleukin-8
  • Plant Extracts
  • Reactive Oxygen Species
  • Solvents
  • Ethanol
  • Matrix Metalloproteinase 9
  • MMP1 protein, human
  • Matrix Metalloproteinase 1