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אסיף מאגר המחקר החקלאי
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Halofuginone, an inhibitor of collagen type I synthesis, prevents postoperative adhesion formation in the rat uterine horn model
Year:
1999
Authors :
Genina, Olga
;
.
Lavelin, Irina
;
.
Pines, Mark
;
.
Volume :
180
Co-Authors:

Nagler, A., The Department of Bone Marrow Transplantation, Hadassah University Hospital, Jerusalem
Genina, O., Institute of Animal Science, ARO, Volcani Center, Bet Dagan 50250, Israel
Lavelin, I., Institute of Animal Science, ARO, Volcani Center, Bet Dagan 50250, Israel
Ohana, M., The Department of Bone Marrow Transplantation, Hadassah University Hospital, Jerusalem
Pines, M., Institute of Animal Science, ARO, Volcani Center, Bet Dagan 50250, Israel

Facilitators :
From page:
558
To page:
563
(
Total pages:
6
)
Abstract:
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.
Note:
Related Files :
animal experiment
Animals
Female
gene expression
Injections, Intraperitoneal
Plant alkaloid
Uterine Diseases
Show More
Related Content
More details
DOI :
10.1016/S0002-9378(99)70254-1
Article number:
0
Affiliations:
Database:
Scopus
Publication Type:
article
;
.
Language:
English
Editors' remarks:
ID:
28049
Last updated date:
02/03/2022 17:27
Creation date:
17/04/2018 00:36
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Scientific Publication
Halofuginone, an inhibitor of collagen type I synthesis, prevents postoperative adhesion formation in the rat uterine horn model
180

Nagler, A., The Department of Bone Marrow Transplantation, Hadassah University Hospital, Jerusalem
Genina, O., Institute of Animal Science, ARO, Volcani Center, Bet Dagan 50250, Israel
Lavelin, I., Institute of Animal Science, ARO, Volcani Center, Bet Dagan 50250, Israel
Ohana, M., The Department of Bone Marrow Transplantation, Hadassah University Hospital, Jerusalem
Pines, M., Institute of Animal Science, ARO, Volcani Center, Bet Dagan 50250, Israel

Halofuginone, an inhibitor of collagen type I synthesis, prevents postoperative adhesion formation in the rat uterine horn model
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.
Scientific Publication
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