Mediators responsible for renal changes in obstructive jaundice are not spe
cified. This study is designed to study the role of endothelin-1 (ET-1) in
obstructive jaundice in rats. Animals were randomly placed into five experi
mental groups. Group 1 (N = 3) was the sham-operated group. Group 2 (N = 8)
after common bile duct (CBD) ligation, received bosentan, which is a nonse
lective endothelin receptor blocker, 50 mg/kg/day for seven days. Group 3 (
N = 7) received 1 mu g/kg/day captopril. Group 4 (N = 7) was given both dru
gs orally for seven days. Group 5 (N = 6) after CBD ligation, received Arab
ic gum as the vehicle. Blood was drawn from the infrahepatic vena cava for
the determination of ET-1, bilirubin, creatinine, protein oxidation product
s, hyaluronic acid, and beta-N-acetyl-hexosaminase. Liver tissue samples we
re obtained to determine glutathione levels. ET-1, protein oxidation produc
ts, hyaluronic acid, bilirubin, and creatinine levels increased significant
ly in the control group when compared with sham. Bosentan effectively preve
nted ET-1 elevation but could not reverse creatinine or bilirubin elevation
. Captopril with or without bosentan was cytoprotective but did not reverse
increased creatinine levels. It is concluded that increased ET-1 in obstru
ctive jaundice may be one of the contributing factors of renal damage.