Degradation of atracurium by Hofmann elimination and ester hydrolysis
depends mainly on pH and temperature and is said to be independent of
liver and kidney function. Consequently atracurium is used widely in p
atients with liver failure. However, there is evidence that incubation
of atracurium at 37 degrees C and pH 8 leads to leakage of LDH from h
epatocyte cell cultures. We have tested the hepatotoxic effects of inc
ubated atracurium in an isolated perfused rat liver model. After equil
ibration, atracurium 2010 mu mol ml(-1) (preincubated at pH 8 and 37 d
egrees C for 120 min) was administered over a period of 10 min followe
d by perfusion of Krebs-Henseleit bicarbonate buffer for 60 min. We fo
und that incubation resulted in considerable degradation of atracurium
and formation of laudanosine. Administration of incubated atracurium
did not produce either biochemical or morphological damage to liver ce
lls, but caused considerable increase in bile flow. We conclude thar a
dministration of preincubated atracurium did nor produce impairment of
liver cell function. The increase in bile flow could be beneficial if
it occurs clinically.