J 2022

Selected ginsenosides interfere efficiently with hepatitis B virus mRNA expression levels and suppress viral surface antigen secretion.

DURAISAMY, Ganesh S., Eunji JO, Ivana HUVAROVÁ, Kyu-Ho P. PARK, Zbyněk HEGER et. al.

Základní údaje

Originální název

Selected ginsenosides interfere efficiently with hepatitis B virus mRNA expression levels and suppress viral surface antigen secretion.

Autoři

DURAISAMY, Ganesh S., Eunji JO, Ivana HUVAROVÁ, Kyu-Ho P. PARK, Zbyněk HEGER, Vojtěch ADAM, Daniel RŮŽEK (203 Česká republika, domácí), Marc P. WINDISCH a Andrew D. MILLER (garant)

Vydání

Heliyon, Elsevier, 2022, 2405-8440

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10606 Microbiology

Stát vydavatele

Velká Británie a Severní Irsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 4.000

Kód RIV

RIV/00216224:14310/22:00126712

Organizační jednotka

Přírodovědecká fakulta

UT WoS

000862260600017

Klíčová slova anglicky

Ginsenoside; Hepatitis B virus; Lamivudine; Nucleoside/nucleotide analogues; Hepatitis B surface protein; Hepatitis B surface antigen; Chronic hepatitis B virus; Drug combinations

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 17. 1. 2023 14:36, Mgr. Marie Šípková, DiS.

Anotace

V originále

Ginsenosides are a class of natural steroid glycosides and triterpene saponins found in Panax ginseng. After screening of a commercial ginsenoside compound library for low cellular cytotoxicity and the ability to mediate efficient reductions in hepatitis B virus (HBV) mRNA expression levels in HepG2.2.15 cells, three ginsenosides (Rg6, Rh4, and Rb3) are selected. Thereafter, using the same cellular model, all three ginsenosides are shown to mediate efficient, selective inhibition of HBV mRNA expression levels, and also interfere with the secretion of both HBV particles and hepatitis B surface antigen (HBsAg). Drug combination studies are performed in both HepG2.2.15 and HBV-infected HepG2-NTCPsec+ cell models with the selected ginsenosides and lamivudine (LMV), a nucleoside analogue used to treat chronic hepatitis B (CHB) infections. These studies, involving RT-qPCR and ELISA, suggest that Rh4/LMV combinations in particular act synergistically to inhibit the secretion of HBV particles and HBsAg. Therefore, on the assumption that appropriate in vivo data are in future agreement, Rh4, in particular, might be used in combination with nucleoside/nucleotide analogues (NUCs) to devise an effective, cost-efficient combination therapy for the treatment of patients with CHB infections.