TY - JOUR
T1 - Halofuginone, an inhibitor of collagen type I synthesis, prevents postoperative adhesion formation in the rat uterine horn model
AU - Nagler, A.
AU - Genina, O.
AU - Lavelin, I.
AU - Ohana, M.
AU - Pines, M.
PY - 1999
Y1 - 1999
N2 - OBJECTIVE: The objective of this study was to evaluate the effects of halofuginone - a specific inhibitor of collagen type I synthesis - in preventing uterine horn adhesion formation in rats. STUDY DESIGN: Adhesions were induced by scraping the rat uterine horns until capillary bleeding occurred. Halofuginone was either injected intraperitoneally or administered orally. The number and severity of the adhesions were scored. Collagen α(l) gene expression was evaluated by in situ hybridization; total collagen was estimated by sirius red staining. Collagen synthesis in response to halofuginone was evaluated in cells cultured from the adhesions. RESULTS: Regardless of the administration procedure, halofuginone reduced significantly the number and severity of the adhesions in a dose-dependent manner. Halofuginone prevented the increase in collagen α1(l) gene expression observed in the rats that underwent this procedure, thus affecting only the newly synthesized collagen but not the resident collagen, in cells derived from rat uterine horn adhesions, halofuginone induced dose-dependent inhibition of collagen synthesis. CONCLUSIONS: Upregulation of collagen synthesis appears to play a critical role in the pathophysiologic mechanism of adhesion formation. Halofuginone could be used as an important means of understanding the role of collagen in adhesion formation and might become a novel and promising antifibrotic agent for preventing adhesion formation after pelvic surgery.
AB - OBJECTIVE: The objective of this study was to evaluate the effects of halofuginone - a specific inhibitor of collagen type I synthesis - in preventing uterine horn adhesion formation in rats. STUDY DESIGN: Adhesions were induced by scraping the rat uterine horns until capillary bleeding occurred. Halofuginone was either injected intraperitoneally or administered orally. The number and severity of the adhesions were scored. Collagen α(l) gene expression was evaluated by in situ hybridization; total collagen was estimated by sirius red staining. Collagen synthesis in response to halofuginone was evaluated in cells cultured from the adhesions. RESULTS: Regardless of the administration procedure, halofuginone reduced significantly the number and severity of the adhesions in a dose-dependent manner. Halofuginone prevented the increase in collagen α1(l) gene expression observed in the rats that underwent this procedure, thus affecting only the newly synthesized collagen but not the resident collagen, in cells derived from rat uterine horn adhesions, halofuginone induced dose-dependent inhibition of collagen synthesis. CONCLUSIONS: Upregulation of collagen synthesis appears to play a critical role in the pathophysiologic mechanism of adhesion formation. Halofuginone could be used as an important means of understanding the role of collagen in adhesion formation and might become a novel and promising antifibrotic agent for preventing adhesion formation after pelvic surgery.
KW - Extracellular matrix
KW - In situ hybridization
KW - Plant alkaloid
KW - Rat adhesions
UR - http://www.scopus.com/inward/record.url?scp=0033054033&partnerID=8YFLogxK
U2 - 10.1016/S0002-9378(99)70254-1
DO - 10.1016/S0002-9378(99)70254-1
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C2 - 10076128
AN - SCOPUS:0033054033
SN - 0002-9378
VL - 180
SP - 558
EP - 563
JO - American Journal of Obstetrics and Gynecology
JF - American Journal of Obstetrics and Gynecology
IS - 3 I
ER -