It has been proposed that oxidative stress is involved in the pathophysiolo
gy of ulcerative colitis. We have reported the depletion of the nonenzymati
c antioxidant, glutathione, in colon from active and inactive ulcerative co
litis. The colon contains several biochemically linked antioxidant systems.
We hypothesized that diminished total antioxidant capacity in active ulcer
ative colitis would be associated with increased colonic lipid peroxidation
. This study was designed to determine total antioxidant capacity and lipid
hydroperoxide levels using colon obtained at surgery from controls (N = 16
; 4 females, 12 males; mean age 70 years), and active and inactive ulcerati
ve colitis (N = 15; 3 females, 12 males; mean age 39). Total antioxidant ca
pacity of control colon was higher in muscularis externa compared to the mu
cosal-submucosal layer (P < 0.05). There were no differences in colonic tot
al antioxidant capacity or lipid hydroperoxide levels comparing control col
on to inactive and active ulcerative colitis. The results did not support d
epletion of tissue total antioxidant capacity by free radicals. Depletion o
f glutathione in ulcerative colitis may be a specific disorder rather than
a secondary defect attributable to global oxidative stress. Nonspecific ant
ioxidant supplements appear unlikely to be beneficial in the treatment of u
lcerative colitis.