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. 2022 Jul 25;11(8):1437. doi: 10.3390/antiox11081437

Table 2.

Antiviral activities of hyperoside (Hyp) in experimental models related to hepatitis B virus (HBV) and hepatitis C virus (HCV) infection.

Hyperoside/Source Experimental Model Dose Results/Molecular Mechanisms References
Hyp/Abelmoschus manihot HepG2.2.15 cells 0.0125, 0.025, 0.05 g/L ↓HBsAg
↓HBeAg
[54]
Hyp/Abelmoschus manihot Ducklings inoculated with duck HBV DNA 0.1 g/kg/day ↓serum HBV DNA [54]
Hyp Duck HBV infection model and normal mouse spleen lymphocyte 25, 50 mg/kg ↓serum HBV DNA
↓hepatic cccDNA
↓Th1 cytokine in normal mouse spleen lymphocyte
[66]
Hyp Ducklings inoculated with duck HBV DNA 300 mg/kg ↓serum HBV DNA
↓rebound of serum HBV DNA compared with lamivudine
[67]
Hyp Huh-7 cells transfected with NS3 gene of HCV Not known ↓HCV NS3 protease by docking the binding sites of NS3 protein [69]

HBV, hepatitis B virus; HCV, hepatitis C virus; NS3, nonstructural protein. Upward pointing arrow (↑) and downward pointing arrow (↓) represent an increase and a decrease in gene/protein expression or numerical values, respectively.