Species Differences of Bile Acid Redox Metabolism: Tertiary Oxidation of Deoxycholate is Conserved in Preclinical Animals

• Published in: Drug metabolism and disposition Vol. 48; no. 6; pp. 499 - 507
• Main Authors: Lin, Qiuhong, Tan, Xianwen, Wang, Wenxia, Zeng, Wushuang, Gui, Lanlan, Su, Mingming, Liu, Changxiao, Jia, Wei, Xu, Liang, Lan, Ke
• Format: Journal Article
• Language: English
• Published: United States The American Society for Pharmacology and Experimental Therapeutics 01.06.2020
• Subjects: Animals; Bile Acids and Salts - analysis; Bile Acids and Salts - chemistry; Bile Acids and Salts - metabolism; Cytochrome P-450 CYP3A - metabolism; Dogs; Drug Evaluation, Preclinical; Feces - chemistry; Female; Germ-Free Life; Humans; Hydroxylation; Male; Mice; Microsomes, Liver; Oxidation-Reduction; Rats; Species Specificity; Stereoisomerism; Substrate Specificity; Tandem Mass Spectrometry; Urine - chemistry
• ISSN: 0090-9556; 1521-009X
• DOI: 10.1124/dmd.120.090464

It was recently disclosed that CYP3A is responsible for the tertiary stereoselective oxidations of deoxycholic acid (DCA), which becomes a continuum mechanism of the host-gut microbial cometabolism of bile acids (BAs) in humans. This work aims to investigate the species differences of BA redox metabolism and clarify whether the tertiary metabolism of DCA is a conserved pathway in preclinical animals. With quantitative determination of the total unconjugated BAs in urine and fecal samples of humans, dogs, rats, and mice, it was confirmed that the tertiary oxidized metabolites of DCA were found in all tested animals, whereas DCA and its oxidized metabolites disappeared in germ-free mice. The in vitro metabolism data of DCA and the other unconjugated BAs in liver microsomes of humans, monkeys, dogs, rats, and mice showed consistencies with the BA-profiling data, confirming that the tertiary oxidation of DCA is a conserved pathway. In liver microsomes of all tested animals, however, the oxidation activities toward DCA were far below the murine-specific 6 -oxidation activities toward chenodeoxycholic acid (CDCA), ursodeoxycholic acid, and lithocholic acid (LCA), and 7-oxidation activities toward murideoxycholic acid and hyodeoxycholic acid came from the 6-hydroxylation of LCA. These findings provided further explanations for why murine animals have significantly enhanced downstream metabolism of CDCA compared with humans. In conclusion, the species differences of BA redox metabolism disclosed in this work will be useful for the interspecies extrapolation of BA biology and toxicology in translational researches. SIGNIFICANCE STATEMENT: It is important to understand the species differences of bile acid metabolism when deciphering biological and hepatotoxicology findings from preclinical studies. However, the species differences of tertiary bile acids are poorly understood compared with primary and secondary bile acids. This work confirms that the tertiary oxidation of deoxycholic acid is conserved among preclinical animals and provides deeper understanding of how and why the downstream metabolism of chenodeoxycholic acid dominates that of cholic acid in murine animals compared with humans.