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February 8, 2026Frontiers in Pharmacology0 citationsOpen Access

Evaluation of Andrographis paniculata in a mouse model of influenza A viral infection using oral administration and a translationally relevant dose

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KSKashif ShamimGBGrace C. BurnettJZJin Zhang

Key Points

  • The aim is to evaluate the effectiveness of Andrographis paniculata against influenza A using a mouse model.
  • Used a standardized commercial extract of A. paniculata containing ≥10% andrographolides.
  • Conducted in vitro tests measuring NF-κB, iNOS, and Nrf2 activities.
  • Employed a non-lethal influenza A mouse model with a treatment group and a control group.
  • Administered the extract orally at a dosage equivalent to recommended human intake for eight days.
  • The extract inhibited NF-κB and iNOS activity while activating Nrf2.
  • A five-fold reduction in lung viral load was observed by day 3 post-infection (p < 0.021) compared to controls.
  • Findings suggest additional active constituents beyond andrographolide are involved.

Abstract

Introduction Ethnobotanically, Andrographis paniculata aerial parts have been used to alleviate the symptoms of viral infections, colds, and sore throats. Although the utility of Andrographis for these indications has had widespread acceptance, multiple knowledge gaps, regarding mechanisms and specific clinical applications, exist for this botanical. Prior rodent studies have limited applicability to inform future clinical applications due to routes of administration used, nonclinical high doses tested, and exclusive evaluation of chemically purified compounds. Methods Experiments used a commercial extract of A. paniculata manufactured from aerial parts that was standardized to contain ≥10% andrographolides. In vitro evaluation measured NF-κB in THP-1 monocytes, iNOS in RAW 264.7 macrophages and Nrf2 in HepG2 cells. In vivo research used a non-lethal influenza A mouse model with two groups ( A. paniculata treatment and vehicle control). Following infection, mice were gavaged daily for 8 days–treatment group received 250 mg extract/kg body weight (dose equivalent to the human label-recommended daily intake). Results The extract inhibited NF-κB and iNOS while activating Nrf2. Although andrographolide contributed to these effects, the findings indicate the presence of additional active constituents that have not yet been characterized. In the mouse model, oral administration of the extract produced a roughly five-fold reduction in lung viral load by day 3 post-infection ( p 0.021) compared with control animals. Discussion Based on the clinically relevant design of our mouse model, the results lay the groundwork for future preclinical research to determine optimal treatment schedule/dosage and immune mechanisms, thereby informing the design for future resilience efficacy clinical trials.

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Cite This Study

Shamim et al. (2026) studied this question.

synapsesocial.com/papers/698828210fc35cd7a88475edhttps://doi.org/10.3389/fphar.2026.1749384
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