Colonic bacteria liberate large quantities of the highly toxic gases hydrog
en sulfide (H2S) and methanethiol (CH3SH). The colonic mucosa presumably ha
s an efficient means of detoxifying these compounds, which is thought to oc
cur through methylation of H2S to CH3SH and CH3SH to dimethylsulfide (CH3SC
H3). We investigated this detoxification pathway by incubating rat cecal mu
cosal homogenates with gas containing H2S, CH3SH, or CH3SCH3. Neither CH3SH
nor CH3SCH3 was produced during H2S catabolism, whereas catabolism of CH3S
H liberated H2S but not CH3SCH3. Thus, H2S and CH3SH are not detoxified by
methylation to CH3SCH3. Rather, CH3SH is demethylated to H2S and H2S is con
verted to nonvolatile metabolites. HPLC analysis of the homogenate showed t
he metabolite to be primarily thiosulfate. Analysis of cecal venous blood o
btained after intracecal instillation of (H2S)-S-35 revealed that virtually
all absorbed H2S had been oxidized to thiosulfate. The oxidation rate of H
2S by colonic mucosa was 10,000 times greater than the reported methylation
rate. Conversion to thiosulfate appears to be the mechanism whereby the ce
cal mucosa protects itself from the injurious effects of H2S and CH3SH, and
defects in this detoxification possibly could play a role in colonic disea
ses such as ulcerative colitis.