Title : Suppression of DHEA sulfotransferase (Sult2A1) during the acute-phase response.

Pub. Date : 2004 Oct

PMID : 15198932






4 Functional Relationships(s)
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1 Recently, the farnesoid X receptor (FXR), constitutive androstane receptor (CAR), and pregnane X receptor (PXR) were found to regulate DHEA sulfotransferase (Sult2A1), which plays an important role in DHEA sulfation and detoxification of bile acids. Dehydroepiandrosterone nuclear receptor subfamily 1 group I member 2 Homo sapiens
2 Recently, the farnesoid X receptor (FXR), constitutive androstane receptor (CAR), and pregnane X receptor (PXR) were found to regulate DHEA sulfotransferase (Sult2A1), which plays an important role in DHEA sulfation and detoxification of bile acids. Dehydroepiandrosterone nuclear receptor subfamily 1 group I member 2 Homo sapiens
3 These results suggest that decreased levels or activities of FXR, PXR, and CAR during the APR could contribute to decreases in Sult2A1, resulting in decreased sulfation of DHEA and lower circulating level of DHEA-S. Dehydroepiandrosterone nuclear receptor subfamily 1 group I member 2 Homo sapiens
4 These results suggest that decreased levels or activities of FXR, PXR, and CAR during the APR could contribute to decreases in Sult2A1, resulting in decreased sulfation of DHEA and lower circulating level of DHEA-S. Dehydroepiandrosterone nuclear receptor subfamily 1 group I member 2 Homo sapiens