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DOI 10.1111/j.1478-3231.2004.0950.x

Медицинская библиотека · Liver international : official journal of the International Association for the Study of the Liver · 2004

Halofuginone can worsen liver fibrosis in bile duct obstructed rats.

Van de Casteele Marc, Roskams Tania, Van der Elst Ingrid, van Pelt Jos F, Fevery Johan, Nevens Frederik

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

BACKGROUND/AIMS: Halofuginone (HF) is an antifibrotic agent in rat models of liver fibrosis caused by repetitive intoxications. A beneficial effect of HF on a biliary type of liver fibrosis has not been proven yet.

METHODS

Bile duct-obstructed rats were given HF from the moment of obstruction onwards and compared with no treatment. After 3 weeks, respectively, 6 weeks, aminopyrine breath test (ABT) and haemodynamic measurements including of portal pressure were carried out. Liver pieces were taken for Sirius red quantitative scoring, as well as for semiquantitative determinations of collagen type I and III RNA levels.

RESULTS

ABT was significantly worse in HF-treated rats as compared with no treatment (P=0.02). Haemodynamic data and collagen type I and III determinations were not significantly different between groups. Biliary fibrosis scores were significantly higher in HF-treated rats as compared with no treatment (P=0.03). More Sirius red staining was associated with more proliferation of bile ductules.

CONCLUSIONS

HF may worsen biliary fibrosis. This contrasts sharply with antifibrotic effects in other models of liver fibrosis. Distinctive cellular mechanisms in biliary fibrosis may explain this discrepancy. One should be cautious for chronic application of HF in man with cholestasis.

Для цитирования: Van de Casteele Marc, Roskams Tania, Van der Elst Ingrid, van Pelt Jos F, Fevery Johan, Nevens Frederik. Halofuginone can worsen liver fibrosis in bile duct obstructed rats.. Liver international : official journal of the International Association for the Study of the Liver. 2004. DOI: 10.1111/j.1478-3231.2004.0950.x.

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