Partial Ligation of the Common Bile Duct Results in Reversible Cholestasis in Rats

被引:1
作者
Jiang, Jun [1 ]
Li, Dongzheng [2 ]
Wei, Jishu [1 ]
Jiang, Kuirong [1 ]
Miao, Yi [1 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Gen Surg, 300 Guangzhou Rd, Nanjing 210029, Jiangsu, Peoples R China
[2] Jiangsu Canc Hosp, Dept Gen Surg, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Cholestasis; Reversible cholestasis; Obstructive jaundice; Experimental study; Animal model; BILIARY OBSTRUCTION; INTRAHEPATIC CHOLESTASIS; LIVER; PROLIFERATION; PATHOGENESIS; EXPRESSION; MECHANISM; INJURY; CELL;
D O I
10.9738/INTSURG-D-15-00164.1
中图分类号
R61 [外科手术学];
学科分类号
摘要
The animal model of common bile duct ligation is very toxic; therefore, the aim of this study was to establish a new model of obstructive jaundice in rats with partial common bile duct obstruction. Male Sprague-Dawley rats were subjected to a sham operation or partial ligation of bile duct procedure. Serum biochemistry, liver histology, and expression of bile salt transporters were examined after surgery. Serum levels of aspartate aminotransferase, alkaline phosphatase, total bilirubin, and bile acids were significantly increased in the partial bile duct ligation group 3 days after surgery. However, these changes spontaneously normalized within 14 days after surgery in the partial bile duct ligation group compared with the sham group. Bile infarcts, ductular reaction, and abundant hepatocyte turnover were detected exclusively in the partial bile duct ligation group on postoperative day 3. However, these changes dramatically reversed 14 days after surgery. Bile salt transporter expression was significantly decreased at day 3 and gradually recovered in the following 2 weeks. In conclusion, the current rat model of obstructive cholestasis is reversible, representing the clinical characteristics of partial biliary obstruction, and may be used to investigate the effects of various therapeutic strategies on reversible acute cholestasis.
引用
收藏
页码:249 / 256
页数:8
相关论文
共 22 条
  • [1] Adaptative bile duct proliferative response in experimental bile duct ischemia
    Beaussier, M
    Wendum, D
    Fouassier, L
    Rey, C
    Barbu, V
    Lasnier, E
    Lienhart, A
    Scoazec, JY
    Rosmorduc, O
    Housset, C
    [J]. JOURNAL OF HEPATOLOGY, 2005, 42 (02) : 257 - 265
  • [2] Bile Formation and Secretion
    Boyer, James L.
    [J]. COMPREHENSIVE PHYSIOLOGY, 2013, 3 (03) : 1035 - 1078
  • [3] Hypoxia-induced changes in the expression of rat hepatobiliary transporter genes
    Fouassier, Laura
    Beaussier, Marc
    Schiffer, Eduardo
    Rey, Colette
    Barbu, Veronique
    Mergey, Martine
    Wendum, Dominique
    Callard, Patrice
    Scoazec, Jean-Yves
    Lasnier, Elisabeth
    Stieger, Bruno
    Lienhart, Andre
    Housset, Chantal
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2007, 293 (01): : G25 - G35
  • [4] Characterization of time-related changes after experimental bile duct ligation
    Georgiev, P.
    Jochum, W.
    Heinrich, S.
    Jang, J. H.
    Nocito, A.
    Dahm, F.
    Clavien, P. -A.
    [J]. BRITISH JOURNAL OF SURGERY, 2008, 95 (05) : 646 - 656
  • [5] Cholestatic hepatocellular injury: what do we know and how should we proceed
    Guicciardi, ME
    Gores, GJ
    [J]. JOURNAL OF HEPATOLOGY, 2005, 42 (03) : 297 - 300
  • [6] The common bile duct ligation in rat:: a relevant in vivo model to study the role of mechanical stress on cell and matrix behaviour
    Guyot, Christelle
    Combe, Chantal
    Desmouliere, Alexis
    [J]. HISTOCHEMISTRY AND CELL BIOLOGY, 2006, 126 (04) : 517 - 523
  • [7] HAMPEL N, 1977, INT SURG, V62, P51
  • [8] Pathogenesis of Cholestatic Liver Disease and Therapeutic Approaches
    Hirschfield, Gideon M.
    Heathcote, E. Jenny
    Gershwin, M. Eric
    [J]. GASTROENTEROLOGY, 2010, 139 (05) : 1481 - 1496
  • [9] Dearterialization of the liver causes intrahepatic cholestasis due to reduced bile transporter expression
    Hoekstra, Harm
    Tian, Yinghua
    Jochum, Wolfram
    Stieger, Bruno
    Graf, Rolf
    Porte, Robert J.
    Clavien, Pierre-Alain
    [J]. TRANSPLANTATION, 2008, 85 (08) : 1159 - 1166
  • [10] HOU CT, 1962, J PATHOL BACTERIOL, V83, P469