Title : Prenatal ethanol exposure increases maternal bile acids through placental transport pathway.

Pub. Date : 2021 Jun 30

PMID : 34217791






4 Functional Relationships(s)
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1 Mining of microarray data from human and rat placental sources identified the involvement of bile acid metabolism and its significant genes, which were verified by RT-qPCR and western blotting on tissues and treated BeWo cells with the administration of FXR/PXR siRNAs or FXR/PXR agonists. Bile Acids and Salts nuclear receptor subfamily 1 group I member 2 Homo sapiens
2 Mining of microarray data from human and rat placental sources identified the involvement of bile acid metabolism and its significant genes, which were verified by RT-qPCR and western blotting on tissues and treated BeWo cells with the administration of FXR/PXR siRNAs or FXR/PXR agonists. Bile Acids and Salts nuclear receptor subfamily 1 group I member 2 Homo sapiens
3 In summary, PEE could induce high bile acid level in maternal serum and its mechanism is associated with the high expression of BCRP/MRP3/OATP2B1 in the placenta through up-regulating PXR and down-regulating FXR, thereby leading to an excessive bile acid transport to maternal blood via the placenta. Bile Acids and Salts nuclear receptor subfamily 1 group I member 2 Homo sapiens
4 In summary, PEE could induce high bile acid level in maternal serum and its mechanism is associated with the high expression of BCRP/MRP3/OATP2B1 in the placenta through up-regulating PXR and down-regulating FXR, thereby leading to an excessive bile acid transport to maternal blood via the placenta. Bile Acids and Salts nuclear receptor subfamily 1 group I member 2 Homo sapiens