Publication: Time course of collagen peak in bile duct-ligated rats
| dc.contributor.authors | Tarcin, Orhan; Basaranoglu, Metin; Tahan, Veysel; Tahan, Gulgun; Sucullu, Ilker; Yilmaz, Nevin; Sood, Gagan; Snyder, Ned; Hilman, Gilbert; Celikel, Cigdem; Tozun, Nurdan | |
| dc.date.accessioned | 2022-03-14T09:29:03Z | |
| dc.date.accessioned | 2026-01-11T14:41:40Z | |
| dc.date.available | 2022-03-14T09:29:03Z | |
| dc.date.issued | 2011-12 | |
| dc.description.abstract | Background: One of the most useful experimental fibrogenesis models is the bile duct-ligated rats. Our aim was to investigate the quantitative hepatic collagen content by two different methods during the different stages of hepatic fibrosis in bile duct-ligated rats on a weekly basis. We questioned whether the 1-wk or 4-wk bile duct-ligated model is suitable in animal fibrogenesis trials. Methods: Of the 53 male Wistar rats, 8 (Group 0) were used as a healthy control group. Bile duct ligation (BDL) had been performed in the rest. Bile duct-ligated rates were sacrificed 7 days later in group 1 (10 rats), 14 days later in group 2 (9 rats), 21 days later in group 3(9 rats) and 28 days later in group 4 (9 rats). Eight rats underwent sham-operation (Sham). Hepatic collagen measurements as well as serum levels of liver enzymes and function tests were all analysed. Results: The peak level of collagen was observed biochemically and histomorphometricly at the end of third week (P < 0.001 and P < 0.05). Suprisingly, collagen levels had decreased with the course of time such as at the end of fourth week (P < 0.01 and P < 0.05). Conclusion: We have shown that fibrosis in bile duct-ligated rats is transient, i.e. reverses spontaneously after 3 weeks. This contrasts any situation in patients where hepatic fibrosis is progressive and irreversible as countless studies performed by many investigators in the same animal model. | |
| dc.identifier.doi | 10.1186/1471-230X-11-45 | |
| dc.identifier.issn | 1471-230X | |
| dc.identifier.pubmed | 21527001 | |
| dc.identifier.uri | https://hdl.handle.net/11424/243180 | |
| dc.identifier.wos | WOS:000291685700001 | |
| dc.language.iso | eng | |
| dc.publisher | BIOMED CENTRAL LTD | |
| dc.relation.ispartof | BMC GASTROENTEROLOGY | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | Bile duct-ligated rat | |
| dc.subject | fibrosis | |
| dc.subject | fibrogenesis | |
| dc.subject | liver | |
| dc.subject | collagen | |
| dc.subject | reversible | |
| dc.subject | BILIARY-OBSTRUCTED RATS | |
| dc.subject | INDUCED LIVER FIBROSIS | |
| dc.subject | HEPATIC-FIBROSIS | |
| dc.subject | INTERFERON-ALPHA | |
| dc.subject | VITAMIN-E | |
| dc.subject | DAMAGE | |
| dc.subject | PROLIDASE | |
| dc.subject | CIRRHOSIS | |
| dc.subject | INJURY | |
| dc.subject | MODEL | |
| dc.title | Time course of collagen peak in bile duct-ligated rats | |
| dc.type | article | |
| dspace.entity.type | Publication | |
| oaire.citation.title | BMC GASTROENTEROLOGY | |
| oaire.citation.volume | 11 |
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