Rat models of advanced cirrhosis, portal hypertension, and renal dysfunction.

  • Victoria K. Snowdon (3801049)
  • Neil J. Lachlan (3801061)
  • Anna M. Hoy (525368)
  • Patrick W. F. Hadoke (206485)
  • Scott I. Semple (312056)
  • Dilip Patel (3801043)
  • Will Mungall (3801058)
  • Timothy J. Kendall (3801022)
  • Adrian Thomson (3801037)
  • Ross J. Lennen (3108276)
  • Maurits A. Jansen (287659)
  • Carmel M. Moran (3801019)
  • Antonella Pellicoro (3801064)
  • Prakash Ramachandran (3801025)
  • Isaac Shaw (3801016)
  • Rebecca L. Aucott (3801031)
  • Thomas Severin (3801055)
  • Rajnish Saini (3801052)
  • Judy Pak (3801034)
  • Denise Yates (3801046)
  • Neelesh Dongre (3801028)
  • Jeremy S. Duffield (335478)
  • David J. Webb (229837)
  • John P. Iredale (515057)
  • Peter C. Hayes (2839478)
  • Jonathan A. Fallowfield (3801040)
Publication date
February 2017

Abstract

<p>Portal pressure (PP; A), renal blood flow (RBF; B), and glomerular filtration rate (GFR; C) in 16-wk CCl<sub>4</sub> and olive oil (OO) control rats (<i>n =</i> 6–11). Representative H&E-stained kidney (scale bar 50 μm) showing minor tubular epithelial cell vacuolation (arrows) without significant necrosis after 16 wk of CCl<sub>4</sub> (D). PP (E), RBF (F), and GFR (G) in bile duct ligation (BDL) and sham-operated (sham) control rats (<i>n =</i> 4–8). Representative H&E-stained kidney (scale bar 50 μm) showing necrotic cells within the tubule lumen and loss of the normal circumferential epithelial cell population (arrows) 4 wk after BDL (H). Data presented as mean ± standard error of the mean, analyzed by one-way ANOVA with post hoc Bon...

Extracted data

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