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Immunomodulatory and anti-SARS activities of Houttuynia cordata. | LitMetric

AI Article Synopsis

  • SARS is a serious pneumonia caused by the SARS coronavirus, affecting over 8000 people globally between late 2002 and mid-2003, primarily in China.
  • The study aimed to investigate how Houttuynia cordata (HC), a traditional remedy, can prevent SARS through immune and antiviral mechanisms.
  • Results indicated that HC enhances immune response by boosting certain T cell populations and cytokine secretion, while also effectively inhibiting key viral enzymes, confirming its safety and potential as a SARS treatment.

Article Abstract

Background: Severe acute respiratory syndrome (SARS) is a life-threatening form of pneumonia caused by SARS coronavirus (SARS-CoV). From late 2002 to mid 2003, it infected more than 8000 people worldwide, of which a majority of cases were found in China. Owing to the absence of definitive therapeutic Western medicines, Houttuynia cordata Thunb. (Saururaceae)(HC) was shortlisted by Chinese scientists to tackle SARS problem as it is conventionally used to treat pneumonia.

Aim Of The Study: The present study aimed to explore the SARS-preventing mechanisms of HC in the immunological and anti-viral aspects.

Results: Results showed that HC water extract could stimulate the proliferation of mouse splenic lymphocytes significantly and dose-dependently. By flow cytometry, it was revealed that HC increased the proportion of CD4(+) and CD8(+) T cells. Moreover, it caused a significant increase in the secretion of IL-2 and IL-10 by mouse splenic lymphocytes. In the anti-viral aspect, HC exhibited significant inhibitory effects on SARS-CoV 3C-like protease (3CL(pro)) and RNA-dependent RNA polymerase (RdRp). On the other hand, oral acute toxicity test demonstrated that HC was non-toxic to laboratory animals following oral administration at 16 g/kg.

Conclusion: The results of this study provided scientific data to support the efficient and safe use of HC to combat SARS.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126383PMC
http://dx.doi.org/10.1016/j.jep.2008.03.018DOI Listing

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