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The study investigates the induction of drug metabolizing enzymes by diaryl pyridines in male rats, focusing on the effects of 2- and 4-substituted isomers. The 2-substituted isomers selectively increased UDP-glucuronosyltransferase activities without inducing cytochrome P450, while some 4-substituted isomers induced both UDP-glucuronosyltransferase and cytochrome P450 activities. The findings suggest that the position of substitution on the pyridine ring is a key factor in determining the selective inducti

Author
shreyakalpesh16
Language
EN

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