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Abstract
1. Urine from goats dosed i.v. With 3-methylindole (3MI; 15 mg/kg) or [methyl-14C] 3MI (15 mg/kg, 0.5 μCi/kg) contained at least 11 metabolites of 3MI.
2. Goat metabolized 3MI to sulfate conjugates of 4- or 7-hydroxy-3-methyloxindole, 5- or 6-hydroxy-3-methyloxindole, and 3,5- or 6-dihydroxy-3-methyloxindole; glucuronic acid conjugates of indole-3-carboxylic acid and 4- or 7-hydrexy-3-methyl-oxindole; and unconjugated 3-hydroxy-3-methyloxindole. Diastereoisomeric glucuronic acid conjugates of 3-hydroxy-3-methyloxindole were also identified in goat urine.
3. Urine from mice dosed i.p. With 3MI (400mg/kg) or [ring-UL-14C] 3MI (400 mg/kg, 125 μCi/kg) contained at least six metabolites of 3MI.
4. Mice metabolized 3MI to glucuronic acid conjugates of 3,5- or 6-dihydroxy-3-methyloxindole, 5- or 6-hydroxy-3-methyloxindole, and indole-3-carboxylic acid; and unconjugated indole-3-carboxylic acid. Unconjugated 3-hydroxy-3-methyloxindole was identified in mouse urine in a previous report.
5. Both goats and mice metabolized 3MI to a mercapturate, 3-[(N-acetyl-L-cystein-S-yl)methyl]indole, which has been previously identified and was confirmed in this study.
6. 3-Methyloxindole was not identified in the urine of either goats or mice.
7. The major pathways of 3MI biotransformation in goats and mice is the formation of mono- and dihydroxy-3-methyloxindoles and their subsequent conjugation with glucuronic acid or sulfate.
8. There are no apparent qualitative differences in the biotransformation of 3MI between goats and mice that can account for their different sensitivities to 3MI induced lung injury.