Studies have found naltrexone useful in the treatment of diseases othe
r than opiate addiction in which endogenous opioids presumably play a
role, such as alcoholism and eating disorders. Some of these studies i
nvolve high doses (100-200 mg bid). Because investigational studies wi
th high doses (300 mg/day) reported clinically significant increases i
n liver enzyme levels, the authors measured a spectrum of liver functi
on parameters in response to high doses of naltrexone in a double-blin
d, crossover trial (100 mg bid) followed by an open-label period (200
mg bid). They observed no adverse clinical or laboratory changes in li
ver function in association with high-dose naltrexone therapy in eatin
g disorders.