1. Academic Validation
  2. A Polysaccharide From Eupolyphaga sinensis Walker With Anti-HBV Activities In Vitro and In Vivo

A Polysaccharide From Eupolyphaga sinensis Walker With Anti-HBV Activities In Vitro and In Vivo

  • Front Pharmacol. 2022 Mar 3;13:827128. doi: 10.3389/fphar.2022.827128.
Xue Zhang 1 Huiling Su 1 Haifei Yu 1 Jialu Ding 1 Wanyu Deng 2 3 Bo Qin 4 Changlin Zhou 1 Jie Dou 1 Min Guo 1
Affiliations

Affiliations

  • 1 State Key Laboratory of Natural Medicines, School of Life Science and Technology, China Pharmaceutical University, Nanjing, China.
  • 2 College of Life Science, Shangrao Normal University, Shangrao, China.
  • 3 Department of Biliary Pancreatic Surgery, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
  • 4 Shaoxing Women and Children's Hospital, Shaoxing, China.
Abstract

Hepatitis B virus (HBV) Infection remains a major global threat to human health worldwide. Recently, the Chinese medicines with Antiviral properties and low toxicity have been a concern. In our previous study, Eupolyphaga sinensis Walker polysaccharide (ESPS) has been isolated and characterized, while its Antiviral effect on HBV remained unclear. The anti-HBV activity of ESPS and its regulatory pathway were investigated in vitro and in vivo. The results showed that ESPS significantly inhibited the production of HBsAg, HBeAg, and HBV DNA in the supernatants of HepG2.2.15 in a dose-dependent manner; HBV RNA and core protein expression were also decreased by ESPS. The in vivo studies using HBV transgenic mice further revealed that ESPS (20 and 40 mg/kg/2 days) significantly reduced the levels HBsAg, HBeAg, and HBV DNA in the serum, as well as HBV DNA and HBV RNA in mice liver. In addition, ESPS activated the Toll-like Receptor 4 (TLR4) pathway; elevated levels of IFN-β, TNF-α, and IL-6 in the serum were observed, indicating that the anti-HBV effect of ESPS was achieved by potentiating innate immunity function. In conclusion, our study shows that ESPS is a potential anti-HBV ingredient and is of great value in the development of new anti-HBV drugs.

Keywords

ESPS; HNF4α; IFN signaling system; Toll-like receptor; anti-HBV activity; pro-inflammatory cytokine.

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