TY - JOUR
T1 - Seprafilm (modified hyaluronic acid and carboxymethylcellulose) acts as a physical barrier
AU - Gago, L. April
AU - Saed, Ghassan M.
AU - Chauhan, Subodhsingh
AU - Elhammady, Eslam F.
AU - Diamond, Michael P.
N1 - Funding Information:
Michael P. Diamond, M.D., is a consultant to Genzyme Corp. and has received research grant support from Genzyme Corp.
PY - 2003/9/1
Y1 - 2003/9/1
N2 - Objective: To characterize the molecular changes that occur in normal fibroblasts, adhesion fibroblasts, and mesothelial cells as a result of exposure to modified hyaluronic acid and carboxymethylcellulose (Seprafilm). Setting: University research laboratory. Design: Human mesothelial and fibroblast cell culture. Main Outcome Measure(s): Multiplex reverse transcriptase polymerase chain reaction was used to examine control and Seprafilm-treated normal peritoneal fibroblasts, adhesion fibroblasts, and mesothelial cells in culture for levels of messenger RNA from molecules known to be associated with adhesion development (transforming growth factor-β1, type I collagen, matrix metalloproteinase-1, matrix metalloproteinase-2, tissue inhibitor of metalloproteinase-1, and tissue plasminogen activator). Result(s): Seprafilm treatment of normal peritoneal fibroblasts, adhesion fibroblasts and mesothelial cells did not alter the expression of markers examined. Conclusion(s): In the absence of a biological effect of Seprafilm on markers known to be involved in postoperative adhesion development, the ability of Seprafilm to reduce postoperative adhesions is most likely caused by its effect as a physical barrier.
AB - Objective: To characterize the molecular changes that occur in normal fibroblasts, adhesion fibroblasts, and mesothelial cells as a result of exposure to modified hyaluronic acid and carboxymethylcellulose (Seprafilm). Setting: University research laboratory. Design: Human mesothelial and fibroblast cell culture. Main Outcome Measure(s): Multiplex reverse transcriptase polymerase chain reaction was used to examine control and Seprafilm-treated normal peritoneal fibroblasts, adhesion fibroblasts, and mesothelial cells in culture for levels of messenger RNA from molecules known to be associated with adhesion development (transforming growth factor-β1, type I collagen, matrix metalloproteinase-1, matrix metalloproteinase-2, tissue inhibitor of metalloproteinase-1, and tissue plasminogen activator). Result(s): Seprafilm treatment of normal peritoneal fibroblasts, adhesion fibroblasts and mesothelial cells did not alter the expression of markers examined. Conclusion(s): In the absence of a biological effect of Seprafilm on markers known to be involved in postoperative adhesion development, the ability of Seprafilm to reduce postoperative adhesions is most likely caused by its effect as a physical barrier.
KW - Adhesion barriers
KW - Adhesion fibroblasts
KW - Adhesions
KW - Matrix metalloproteinase-1
KW - Matrix metalloproteinase-2
KW - Seprafilm
KW - Tissue inhibitor of metalloproteinase-1
KW - Tissue plasminogen activator
KW - Transforming growth factor-β1
KW - Type I collagen
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U2 - 10.1016/S0015-0282(03)00767-2
DO - 10.1016/S0015-0282(03)00767-2
M3 - Article
C2 - 12969707
AN - SCOPUS:0041334200
SN - 0015-0282
VL - 80
SP - 612
EP - 616
JO - Fertility and Sterility
JF - Fertility and Sterility
IS - 3
ER -