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Antiviral effect of an extract from Kaempferia galanga L. rhizome in mice infected with pseudorabies virus. | LitMetric

AI Article Synopsis

  • Pseudorabies virus (PrV) causes serious diseases in various mammals and birds, highlighting the need for effective control measures.
  • An extract from the rhizome of Kaempferia galanga L (Kge), containing flavonoids and other compounds, showed strong anti-PrV activity, significantly reducing cell death in infected PK-15 cells.
  • In studies with PrV-infected mice, Kge improved survival rates and reduced virus levels in the brain, while also decreasing tissue damage and modulating immune responses, making it a potential treatment for PrV infections.

Article Abstract

Pseudorabies virus (PrV) is one of the most important herpesviruses which can cause severe diseases in many mammals and some avian species. In recent years, repeated outbreaks of pseudorabies worldwide indicated an urgent need for new control measures. The results described in this study demonstrated that an extract prepared from the rhizome of Kaempferia galanga L (Kge), which consisted of flavonoids (2.82%), saccharides (61.37%), phenols (1.22%) and saponins (3.10%), possessed a potent anti-PrV activity. In PK-15 cells, Kge treatment inhibited PrV-induced cell death by more than 90% at a dose of 200 μg/mL. The 50% inhibitory concentration (IC) was 55.85 μg/mL. In the PrV-infected mice treated with Kge, the survival rate was up to 60% at day 6 post-infection, while the infected mice without Kge treatment all died. The virus titers in the brains of the Kge-treated infected mice were significantly reduced. Kge treatment also alleviated the severity of the PrV-induced lesions in the heart, liver, spleen, lung and kidney. Kge exhibited immune-regulating activity through the regulation of cytokines (IFN-α, IFN-β, IL-4, IL-6 and TNF-α) in the serum of PrV-infected mice, suggesting that one possible mechanism of anti-PrV activity was through the regulation of immune function. These results suggested that Kge could be a promising drug candidate for treating PrV infections.

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Source
http://dx.doi.org/10.1016/j.jviromet.2022.114573DOI Listing

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