In an earlier study we showed that bile duct-ligated rats were highly
susceptible to gentamicin nephrotoxicity and that oral calcium adminis
tration had a pronounced protective effect. The mechanism by which thi
s occurs is unclear. Because cations compete with gentamicin for tubul
e binding sites, it has been suggested that the increased susceptibili
ty of the kidney to gentamicin after bile duct ligation might result f
rom decreased cation excretion. The aim of this study was to determine
the effect of bile duct ligation on calcium excretion in relation to
overall renal function. Male Sprague-Dawley rats underwent bile duct l
igation and division. Pair fed sham-operated rats served as controls.
Metabolic and clearance studies were carried out at 3, 5, 7, 14 and 21
days after surgery. Urine output was higher in bile duct-ligated rats
, and they excreted more calcium at 3, 5, 7 and 14 days, while excreti
ng less sodium than controls. We conclude that after bile duct ligatio
n, there is increased calcium excretion, which is independent of the a
bnormality in sodium excretion. Enhanced nephrotoxicity with aminoglyc
osides in the bile duct-ligated rat model cannot be explained by decre
ased calcium excretion.