Animal models resembling the human situation are very useful to invest
igate human disease. However, there has been no evidence of esophageal
varices in rats with liver cirrhosis. In the present study, to determ
ine whether intrahepatic portal hypertension produced by liver cirrhos
is induces esophageal varices in rats, the esophagus was examined endo
scopically in rat models of liver cirrhosis. All rats given carbon tet
rachloride or thioacetamide and six of seven rats given a choline-defi
cient diet had esophageal varices or Venous dilatation after 16 weeks
of treatment, although the varices In one rat given carbon tetrachlori
de and in two rats given a choline-deficient diet were reduced from we
eks 16 to 18. These findings suggest that timing is important when stu
dying esophageal varices in rat models of liver cirrhosis. II is concl
uded that certain models of liver cirrhosis in rats could be used as m
odels of esophageal varices due to intrahepatic portal hypertension.