Je. Sutherland et al., BILE IS AN IMPORTANT ROUTE OF ELIMINATION OF INGESTED ALUMINUM BY CONSCIOUS MALE SPRAGUE-DAWLEY RATS, Toxicology, 109(2-3), 1996, pp. 101-109
We assessed the importance of bile as an excretory route for ingested
aluminum (Al). Bile ducts in 30 male Sprague-Dawley rats were cannulat
ed to allow both bile collection and reinfusion of bile acids. Five da
ys after surgery, rats (average weight = 191 +/- 4 g) were given a sin
gle oral dose of aluminum (0, 0.2, 0.4, or 0.8 mmol) as aluminum lacta
te in 1 mi of 16% citrate by gavage. Bile was collected 1-7 h after do
sing from unanesthetized rats. Biliary aluminum secretion was highest
during the first hour of bile collection. All rats dosed with aluminum
secreted significantly greater amounts of aluminum in bile than contr
ol rats. However, biliary aluminum secretion did not vary among animal
s given the different aluminum doses suggesting that biliary secretion
of aluminum was saturated at these doses. Rats dosed with 0.8 mmol Al
retained significantly greater amounts of aluminum in soft tissues th
an those given 0.2 or 0.4 mmol Al, This result suggests that physiolog
ical mechanisms were unable to prevent tissue aluminum accumulation in
the rats given the highest dose.