Title : Cholangiopathy and Biliary Fibrosis in Cyp2c70-Deficient Mice Are Fully Reversed by Ursodeoxycholic Acid.

Pub. Date : 2021

PMID : 33309945






8 Functional Relationships(s)
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1 Cholangiopathy and biliary fibrosis in Cyp2c70-deficient mice are fully reversed by ursodeoxycholic acid. Ursodeoxycholic Acid cytochrome P450, family 2, subfamily c, polypeptide 70 Mus musculus
2 Cyp2c70-ablation in mice prevents synthesis of mouse/rat-specific muricholic acids (MCAs), but potential (patho)physiological consequences of their absence are unknown. muricholic acid cytochrome P450, family 2, subfamily c, polypeptide 70 Mus musculus
3 Cyp2c70-ablation in mice prevents synthesis of mouse/rat-specific muricholic acids (MCAs), but potential (patho)physiological consequences of their absence are unknown. muricholic acid cytochrome P450, family 2, subfamily c, polypeptide 70 Mus musculus
4 RESULTS: Cyp2c70-/- mice were devoid of MCAs and showed high abundances of chenodeoxycholic and lithocholic acids. chenodeoxycholic cytochrome P450, family 2, subfamily c, polypeptide 70 Mus musculus
5 RESULTS: Cyp2c70-/- mice were devoid of MCAs and showed high abundances of chenodeoxycholic and lithocholic acids. Lithocholic Acid cytochrome P450, family 2, subfamily c, polypeptide 70 Mus musculus
6 Addition of 0.1% ursodeoxycholic acid to the diet fully normalized hepatic and intestinal functions in female Cyp2c70-/- mice. Ursodeoxycholic Acid cytochrome P450, family 2, subfamily c, polypeptide 70 Mus musculus
7 These consequences of Cyp2c70-deficiency are restored by treatment with UDCA, indicating a role of BA hydrophobicity in disease development. Ursodeoxycholic Acid cytochrome P450, family 2, subfamily c, polypeptide 70 Mus musculus
8 These consequences of Cyp2c70-deficiency are restored by treatment with UDCA, indicating a role of BA hydrophobicity in disease development. Bile Acids and Salts cytochrome P450, family 2, subfamily c, polypeptide 70 Mus musculus