Serum Prolidase and IGF-1 as Non-invasive Markers of Hepatic Fibrosis During Four Different Periods After Bile-duct Ligation in Rats

Aim Our aim was to study the correlation of serum prolidase and insulin like growth factor-1 to liver collagen and assess their utility as markers of fibrosis during four different periods of hepatic injury and fibrosis after bile-duct ligation in rats. Methods Forty-eight Wistar albino rats were in...

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Published in:Digestive diseases and sciences Vol. 53; no. 7; pp. 1938 - 1945
Main Authors: Tarçın, Orhan, Gedik, Nursal, Karakoyun, Berna, Tahan, Veysel, Sood, Gagan, Çelikel, Çiğdem, Tözün, Nurdan
Format: Journal Article
Language:English
Published: Boston Springer US 01-07-2008
Springer
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Summary:Aim Our aim was to study the correlation of serum prolidase and insulin like growth factor-1 to liver collagen and assess their utility as markers of fibrosis during four different periods of hepatic injury and fibrosis after bile-duct ligation in rats. Methods Forty-eight Wistar albino rats were included in the study and divided into six groups. Seven rats served as the control group (Control), while seven rats had a sham operation (Sham group). Thirty-four rats underwent bile-duct ligation. Bile-duct ligated (BDL) animals were sacrificed at the end of the first week (Group 1; n  = 8), second week (Group 2; n  = 8), third week (Group 3; n  = 9), or fourth week (Group 4; n  = 9) after BDL. Liver collagen, liver prolidase, and serum prolidase and IGF-I, were determined. Results There was a positive correlation between liver collagen and serum prolidase (r s : 0.843, P  < 0.001) levels and a negative correlation among liver collagen and serum IGF-1 levels (r s : −0.667, P  < 0.001). The peak levels of liver collagen and serum prolidase were reached in the third week while the lowest levels of IGF-1 were found at the end of the third week. Conclusion Serum prolidase and IGF-1 either independently or in combination correlate with liver collagen content in hepatic fibrosis.
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ISSN:0163-2116
1573-2568
DOI:10.1007/s10620-007-0073-1