Title : In vitro and in vivo approaches for identifying the role of aryl hydrocarbon receptor in the development of nonalcoholic fatty liver disease.

Pub. Date : 2020 Feb 1

PMID : 31730885






5 Functional Relationships(s)
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1 In present study, we used benzo[a]pyrene (BaP), a classic and potent ligand of AhR, to activate AhR pathway causes overexpression of the estrogen-metabolizing enzyme cytochrome P450 1A1 (CYP1A1) and affects the expression of important genes involved in hepatic lipid regulation. Benzo(a)pyrene cytochrome P450 family 1 subfamily A member 1 Homo sapiens
2 In present study, we used benzo[a]pyrene (BaP), a classic and potent ligand of AhR, to activate AhR pathway causes overexpression of the estrogen-metabolizing enzyme cytochrome P450 1A1 (CYP1A1) and affects the expression of important genes involved in hepatic lipid regulation. Benzo(a)pyrene cytochrome P450 family 1 subfamily A member 1 Homo sapiens
3 In present study, we used benzo[a]pyrene (BaP), a classic and potent ligand of AhR, to activate AhR pathway causes overexpression of the estrogen-metabolizing enzyme cytochrome P450 1A1 (CYP1A1) and affects the expression of important genes involved in hepatic lipid regulation. Benzo(a)pyrene cytochrome P450 family 1 subfamily A member 1 Homo sapiens
4 In present study, we used benzo[a]pyrene (BaP), a classic and potent ligand of AhR, to activate AhR pathway causes overexpression of the estrogen-metabolizing enzyme cytochrome P450 1A1 (CYP1A1) and affects the expression of important genes involved in hepatic lipid regulation. Benzo(a)pyrene cytochrome P450 family 1 subfamily A member 1 Homo sapiens
5 BaP induces CYP1A1 expression through AhR signaling and inhibits the protective effect of 17beta-estradiol (E2) on hepatic steatosis, characterized by triglyceride accumulation, and markers of liver damage are significantly elevated. Benzo(a)pyrene cytochrome P450 family 1 subfamily A member 1 Homo sapiens