Reduced hepatitis B and D viral entry using clinically applied drugs as novel inhibitors of the bile acid transporter NTCP.

Article Details

Citation

Donkers JM, Zehnder B, van Westen GJP, Kwakkenbos MJ, IJzerman AP, Oude Elferink RPJ, Beuers U, Urban S, van de Graaf SFJ

Reduced hepatitis B and D viral entry using clinically applied drugs as novel inhibitors of the bile acid transporter NTCP.

Sci Rep. 2017 Nov 10;7(1):15307. doi: 10.1038/s41598-017-15338-0.

PubMed ID
29127322 [ View in PubMed
]
Abstract

The sodium taurocholate co-transporting polypeptide (NTCP, SLC10A1) is the main hepatic transporter of conjugated bile acids, and the entry receptor for hepatitis B virus (HBV) and hepatitis delta virus (HDV). Myrcludex B, a synthetic peptide mimicking the NTCP-binding domain of HBV, effectively blocks HBV and HDV infection. In addition, Myrcludex B inhibits NTCP-mediated bile acid uptake, suggesting that also other NTCP inhibitors could potentially be a novel treatment of HBV/HDV infection. This study aims to identify clinically-applied compounds intervening with NTCP-mediated bile acid transport and HBV/HDV infection. 1280 FDA/EMA-approved drugs were screened to identify compounds that reduce uptake of taurocholic acid and lower Myrcludex B-binding in U2OS cells stably expressing human NTCP. HBV/HDV viral entry inhibition was studied in HepaRG cells. The four most potent inhibitors of human NTCP were rosiglitazone (IC(50) 5.1 microM), zafirlukast (IC(50) 6.5 microM), TRIAC (IC(50) 6.9 microM), and sulfasalazine (IC(50) 9.6 microM). Chicago sky blue 6B (IC(50) 7.1 microM) inhibited both NTCP and ASBT, a distinct though related bile acid transporter. Rosiglitazone, zafirlukast, TRIAC, sulfasalazine, and chicago sky blue 6B reduced HBV/HDV infection in HepaRG cells in a dose-dependent manner. Five out of 1280 clinically approved drugs were identified that inhibit NTCP-mediated bile acid uptake and HBV/HDV infection in vitro.

DrugBank Data that Cites this Article

Drug Transporters
DrugTransporterKindOrganismPharmacological ActionActions
RosiglitazoneSodium/bile acid cotransporterProteinHumans
Unknown
Inhibitor
Details
SulfasalazineSodium/bile acid cotransporterProteinHumans
Unknown
Inhibitor
Details
TiratricolSodium/bile acid cotransporterProteinHumans
Unknown
Inhibitor
Details
ZafirlukastSodium/bile acid cotransporterProteinHumans
Unknown
Inhibitor
Details