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Ce produit n'est pas destiné à diagnostiquer, traiter, guérir ou prévenir toute maladie. Ces déclarations n'ont pas été évaluées par la Food and Drug Administration.
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Ces informations sont fournies à titre éducatif uniquement et ne remplacent pas un avis médical professionnel, un diagnostic ou un traitement. Consultez toujours votre professionnel de santé avant d'utiliser des plantes, surtout si vous êtes enceinte, allaitez, prenez des médicaments ou avez une condition médicale.
Tasmannia lanceolata
Australian native shrub used by Aboriginal Tasmanians as a spice and medicine, with strong antimicrobial and anti-inflammatory properties from polygodial.
Mountain Pepper (Tasmannia lanceolata) is an Australian native shrub traditionally used by Aboriginal peoples as a spice and medicine. Its primary active compounds, including polygodial and other sesquiterpene dialdehydes, exhibit strong antimicrobial, anti-inflammatory, and antioxidant properties. Evidence is limited to preclinical and traditional use (Level C).
Polygodial, a sesquiterpene dialdehyde, disrupts microbial cell membranes and inhibits fungal growth by binding to ergosterol. It also modulates inflammatory pathways by inhibiting NF-κB activation and COX-2 expression, reducing prostaglandin synthesis. Additionally, it activates TRPA1 and TRPV1 receptors, contributing to its pungent and potential analgesic effects.
Australian native shrub used by Aboriginal Tasmanians as a spice and medicine, with strong antimicrobial and anti-inflammatory properties from polygodial.
Mountain Pepper (Tasmannia lanceolata) is an Australian native shrub traditionally used by Aboriginal peoples as a spice and medicine. Its primary active compounds, including polygodial and other sesquiterpene dialdehydes, exhibit strong antimicrobial, anti-inflammatory, and antioxidant properties. Evidence is limited to preclinical and traditional use (Level C).
Polygodial, a sesquiterpene dialdehyde, disrupts microbial cell membranes and inhibits fungal growth by binding to ergosterol. It also modulates inflammatory pathways by inhibiting NF-κB activation and COX-2 expression, reducing prostaglandin synthesis. Additionally, it activates TRPA1 and TRPV1 receptors, contributing to its pungent and potential analgesic effects.