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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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Desmodium gangeticum
One of the Dashamoola (ten root) Ayurvedic herbs, used for nervous system, musculoskeletal conditions, and as a tonic.
Shalaparni (Desmodium gangeticum) is a foundational herb in Ayurveda, particularly valued as one of the Dashamoola roots for its adaptogenic, anti-inflammatory, and nervine tonic properties. Its primary active compounds include indole-3-alkylamines, gangetin, desmodin, and serotonin derivatives, which contribute to its traditional uses in supporting the nervous system, alleviating joint pain, and reducing fever.
The adaptogenic effects of Desmodium gangeticum are attributed to its modulation of the hypothalamic-pituitary-adrenal (HPA) axis, reducing cortisol levels and enhancing stress resilience. Its anti-inflammatory and analgesic actions involve inhibition of cyclooxygenase (COX) and lipoxygenase (LOX) pathways, as well as suppression of pro-inflammatory cytokines such as TNF-α and IL-6. The serotonin derivatives and phenylethylamine content may contribute to its nervine and mood-stabilizing properties by interacting with serotonin and dopamine receptors.
One of the Dashamoola (ten root) Ayurvedic herbs, used for nervous system, musculoskeletal conditions, and as a tonic.
Shalaparni (Desmodium gangeticum) is a foundational herb in Ayurveda, particularly valued as one of the Dashamoola roots for its adaptogenic, anti-inflammatory, and nervine tonic properties. Its primary active compounds include indole-3-alkylamines, gangetin, desmodin, and serotonin derivatives, which contribute to its traditional uses in supporting the nervous system, alleviating joint pain, and reducing fever.
The adaptogenic effects of Desmodium gangeticum are attributed to its modulation of the hypothalamic-pituitary-adrenal (HPA) axis, reducing cortisol levels and enhancing stress resilience. Its anti-inflammatory and analgesic actions involve inhibition of cyclooxygenase (COX) and lipoxygenase (LOX) pathways, as well as suppression of pro-inflammatory cytokines such as TNF-α and IL-6. The serotonin derivatives and phenylethylamine content may contribute to its nervine and mood-stabilizing properties by interacting with serotonin and dopamine receptors.