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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.
Nymphaea lotus
An Egyptian water lily with sacred significance used in traditional medicine as a sedative and aphrodisiac.
Nymphaea lotus, an Egyptian water lily, is traditionally used as a sedative and aphrodisiac. Its pharmacological activity is attributed to nuciferine, aporphine alkaloids, and flavonoids, which exhibit anxiolytic, anti-inflammatory, and antispasmodic effects in preliminary studies. Evidence is limited to pilot and traditional use, with no large-scale clinical trials.
Nuciferine acts as a partial agonist at serotonin 5-HT1A and 5-HT2A receptors, contributing to anxiolytic and sedative effects. Aporphine alkaloids inhibit phosphodiesterase-4 (PDE4) and modulate dopamine D1 and D2 receptors, potentially explaining aphrodisiac and mood-elevating properties. Flavonoids and tannins provide anti-inflammatory activity via COX-2 inhibition and antioxidant pathways, while antispasmodic effects are mediated through calcium channel blockade in smooth muscle.
An Egyptian water lily with sacred significance used in traditional medicine as a sedative and aphrodisiac.
Nymphaea lotus, an Egyptian water lily, is traditionally used as a sedative and aphrodisiac. Its pharmacological activity is attributed to nuciferine, aporphine alkaloids, and flavonoids, which exhibit anxiolytic, anti-inflammatory, and antispasmodic effects in preliminary studies. Evidence is limited to pilot and traditional use, with no large-scale clinical trials.
Nuciferine acts as a partial agonist at serotonin 5-HT1A and 5-HT2A receptors, contributing to anxiolytic and sedative effects. Aporphine alkaloids inhibit phosphodiesterase-4 (PDE4) and modulate dopamine D1 and D2 receptors, potentially explaining aphrodisiac and mood-elevating properties. Flavonoids and tannins provide anti-inflammatory activity via COX-2 inhibition and antioxidant pathways, while antispasmodic effects are mediated through calcium channel blockade in smooth muscle.