Ozone is one of the most powerful oxidants available, with many application
s in industry and medicine. Medically relevant features of ozone include ba
cterial and virucidal properties, disinfection, sterilization, circulatory
stimulation, and disruption of malignant cells. Ozone therapy is administer
ed in various ways, including intravenously; intramuscularly, and intrarect
ally. The latter modality is used for the treatment of colitis and hepatiti
s. Our aim was to examine the effect of ozone water enema on normal and inf
lamed rat colonic mucosa. Ozone water (20 mug/ml) was prepared via ozone ge
nerator and administered intrarectally (0.5 ml) daily. Rats were killed one
, three, and seven days after rectal ozone water administration, and their
colons resected, rinsed, and weighed (grams per 10 cm). Damage was assessed
macro- and microscopically and tissue processed for myeloperoxidase and ni
tric oxide synthase activity. Rats receiving saline served as controls. In
an additional experiment colitis was induced by intrarectal iodoacetamide.
Ozone therapy caused no macroscopic damage. Ozone therapy induced microscop
ic colitis, which lasted for at least a week and was accompanied by increas
e in segmental weight, myeloperoxidase and nitric oxide activity, and prost
aglandin E-2 generation. Ozone therapy had no protective effect on inflamed
mucosa. In conclusion, ozone water therapy had a deleterious effect on nor
mal colonic mucosa, suggesting intrarectal administration be reevaluated. O
zone water enema may serve as a model of microscopic colitis.