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1455691 
Journal Article 
Regulatory Action of Charred Gossamer Urocteae on the Functions of Mouse Oral Fibroblasts 
Dai Jian-ping; Chen Jun; Han Bang-xing; Bei Yu-fei; Zhou Xiao-kun 
2010 
30 
126-131 
English 
OBJECTIVE: To explore the influence of charred Gossamer urocteae (CGU) on the functions of primary cultured mouse oral fibroblasts and reveal its mechanism in wound healing.

METHODS: CGU was extracted with different solvents and ethanol extract (EE), ethyl acetate fraction (EF), n-butanol fraction (BF) and aqueous fraction (AF) were obtained. The effects of different fractions on the proliferation, matrix metalloproteinase-2,9 (MMP-2,9) activities, synthesis of collagen and tissue inhibitor of metalloproteinase 1 (TIMP-1) in the mouse oral fibroblasts were determined by MTT, gelatin zymography, chloramine-T method, and enzyme-linked immunosorbent assay (ELISA) respectively.

RESULTS: EE, EF and BF at high concentrations could significantly inhibit proliferation of fibroblasts (P<0.05 or P<0.01), and at low concentrations EF and BF could promote proliferation of fibroblasts, and BF and AF could significantly inhibit collagen synthesis (P<0.05 or P<0.01). EE, EF and AF at high concentrations could significantly increase the MMP-9 activity, and BF and AF could significantly inhibit synthesis of TIMP-1.

CONCLUSION: CGU at high concentrations can inhibit the proliferations of fibroblasts and synthesis of collagen, and in healing of wound, CGU at high concentrations possibly has the functions of anti-fibrosis and anti-scar, and the mechanism to promote degradation of collagen is possibly related to the increase in MMP-9 activity and the inhibition of TIMP-1 synthesis. 
collagen synthesis; mouse oral fibroblast; matrix metalloproteinase-2,9 (MMP-2,9); tissue inhibitor of metalloproteinase 1 (TIMP-1) 
IRIS
• n-Butanol
     Database searches
          WOS
     Source – January 2013 (private)
          WOS - 1/2013
          Merged reference set - 1/2013
     Excluded (not pertinent)
          Not chemical specific