Title : Short-term obeticholic acid treatment does not impact cholangiopathy in Cyp2c70-deficient mice with a human-like bile acid composition.

Pub. Date : 2022 Aug

PMID : 35470044






10 Functional Relationships(s)
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1 Cyp2c70-/- mice with a human-like bile acid (BA) composition, lacking hydrophilic muricholic acids (MCAs), have been reported to display cholangiopathy and biliary fibrosis with female preponderance that can be reversed by ursodeoxycholic acid (UDCA). Bile Acids and Salts cytochrome P450, family 2, subfamily c, polypeptide 70 Mus musculus
2 Cyp2c70-/- mice with a human-like bile acid (BA) composition, lacking hydrophilic muricholic acids (MCAs), have been reported to display cholangiopathy and biliary fibrosis with female preponderance that can be reversed by ursodeoxycholic acid (UDCA). Bile Acids and Salts cytochrome P450, family 2, subfamily c, polypeptide 70 Mus musculus
3 Cyp2c70-/- mice with a human-like bile acid (BA) composition, lacking hydrophilic muricholic acids (MCAs), have been reported to display cholangiopathy and biliary fibrosis with female preponderance that can be reversed by ursodeoxycholic acid (UDCA). muricholic acid cytochrome P450, family 2, subfamily c, polypeptide 70 Mus musculus
4 Cyp2c70-/- mice with a human-like bile acid (BA) composition, lacking hydrophilic muricholic acids (MCAs), have been reported to display cholangiopathy and biliary fibrosis with female preponderance that can be reversed by ursodeoxycholic acid (UDCA). Ursodeoxycholic Acid cytochrome P450, family 2, subfamily c, polypeptide 70 Mus musculus
5 Cyp2c70-/- mice with a human-like bile acid (BA) composition, lacking hydrophilic muricholic acids (MCAs), have been reported to display cholangiopathy and biliary fibrosis with female preponderance that can be reversed by ursodeoxycholic acid (UDCA). Ursodeoxycholic Acid cytochrome P450, family 2, subfamily c, polypeptide 70 Mus musculus
6 In Cyp2c70-/- mice, however, BA pool became more hydrophobic with a larger proportion of chenodeoxycholic acid, attributable to a reduction of BA 12alpha-hydroxylation. Bile Acids and Salts cytochrome P450, family 2, subfamily c, polypeptide 70 Mus musculus
7 In Cyp2c70-/- mice, however, BA pool became more hydrophobic with a larger proportion of chenodeoxycholic acid, attributable to a reduction of BA 12alpha-hydroxylation. Chenodeoxycholic Acid cytochrome P450, family 2, subfamily c, polypeptide 70 Mus musculus
8 In Cyp2c70-/- mice, however, BA pool became more hydrophobic with a larger proportion of chenodeoxycholic acid, attributable to a reduction of BA 12alpha-hydroxylation. Bile Acids and Salts cytochrome P450, family 2, subfamily c, polypeptide 70 Mus musculus
9 In conclusion, 4 weeks of OCA treatment oppositely modulates the hydrophobicity of the BA pool in WT and Cyp2c70-/- mice, but does not improve or worsen the characteristic sex-dependent liver pathology in Cyp2c70-/- mice. obeticholic acid cytochrome P450, family 2, subfamily c, polypeptide 70 Mus musculus
10 In conclusion, 4 weeks of OCA treatment oppositely modulates the hydrophobicity of the BA pool in WT and Cyp2c70-/- mice, but does not improve or worsen the characteristic sex-dependent liver pathology in Cyp2c70-/- mice. Bile Acids and Salts cytochrome P450, family 2, subfamily c, polypeptide 70 Mus musculus