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Chinese Journal of Burns ; (6): 427-430, 2006.
Article in Chinese | WPRIM | ID: wpr-331553

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the influence of the vascular endothelial growth factor( VEGF) antibody targeted vascular therapy on the expression of human collagen type I in hyperplastic scar of nude mice.</p><p><b>METHODS</b>The hyperplastic scar from one female burn patient with 1% TBSA deep-partial thickness burns were implanted into subcutaneous skin of scapular region of 48 nude mice. Three weeks later, the nude mice were divide into large dose (LA) , medium dose (MD) , small dose (SD) and control groups, with 12 mice in each group. The mice in LA,MD and SD groups were injected with 200 microl of 15,10, 5 microg/ml VEGF monoclonal antibody diluted in 0.01 mol/L PBS, respectively in the scar twice a week for 3 weeks, while those in C group were injected with equal amount of 0. 01 mol/L PBS. The area and volume of the scar in each group were calculated and histological changes were observed, and the expression of collagen type I mRNA and its protein in each group were determined 3 days after treatment.</p><p><b>RESULTS</b>The volume of scar in LA, MD, SD and C groups were (55.3 +/-4.1, 67.9 +/-5.7, 78.9 +/-5.5, 85.0 +7.3) mm(3), respectively. Compared with that in C group, the volume of the scar were significantly decreased in AD and MD groups ( P <0.05). A few number of vessels and fibroblasts were observed in LD, MD groups, with decreased number of collagen fibers arranged in order. Compared with that in C group ,The expression of procollagen type I mRNA and its protein in C group was obviously higher than those in LD and MD groups ( P < 0. 05) , but it was similar to those in SD group.</p><p><b>CONCLUSION</b>VEGF targeted vascular therapy is beneficial for the inhibition of the angiopoietins of hyperplastic scar, the expression of collagen , and the growth of scar.</p>


Subject(s)
Adult , Animals , Female , Humans , Mice , Antibodies, Monoclonal , Therapeutic Uses , Cicatrix, Hypertrophic , Metabolism , Therapeutics , Collagen Type I , Metabolism , Disease Models, Animal , Gene Expression , Hyperplasia , Metabolism , Therapeutics , Mice, Inbred BALB C , Mice, Nude , Neovascularization, Pathologic , Metabolism , RNA, Messenger , Metabolism , Vascular Endothelial Growth Factor A , Allergy and Immunology
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