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Rutin (Quercetin-3-O-rutinoside)

Preliminary

Mechanism of Action

Antioxidant via free radical scavenging and metal chelation; anti-inflammatory through NF-κB and COX-2 inhibition; capillary-strengthening via inhibition of hyaluronidase; antiplatelet via TXA2 inhibition; mild ACE inhibitory activity
Rutin is a flavonoid glycoside of quercetin linked to the disaccharide rutinose (6-O-α-L-rhamnosyl-β-D-glucose). Following oral ingestion, rutin is hydrolyzed by gut microbial beta-glucosidase and alpha-rhamnosidase enzymes to release quercetin aglycone, which is then absorbed in the small intestine. Quercetin inhibits aldose reductase (reducing sorbitol accumulation in diabetic complications), inhibits phosphodiesterase (elevating cAMP), stabilizes mast cells (reducing allergic mediator release), and inhibits poly(ADP-ribose) polymerase (PARP), providing cytoprotection under oxidative stress. Capillary-strengthening effects occur through inhibition of hyaluronidase, preservation of collagen matrix integrity, and reduction of vascular smooth muscle contraction via calcium antagonism. Anti-platelet activity (inhibition of ADP and collagen-induced aggregation) contributes to the cardiovascular protective profile.

Research Notes

Rutin demonstrates consistent anti-inflammatory and vascular-protective effects across multiple in vitro and animal studies. Clinical data for rutin alone limited; pharmacokinetic studies confirm systemic absorption following oral administration. Capillary fragility reduction documented in clinical studies. Antioxidant activity confirmed in human supplementation studies.

TarragonWestern

Clinical trials on rutin are most robust for venous insufficiency and capillary fragility: a double-blind RCT (n=40) found 500 mg rutin twice daily significantly reduced capillary fragility and lower limb edema over 6 weeks versus placebo. Animal studies confirm rutin's antidiabetic activity: 100 mg/kg/day reduced HbA1c by 1.8% and improved kidney function markers in streptozotocin diabetic rats over 30 days. Meta-analyses of dietary flavonoid intake (including rutin-containing foods) associate higher intake with 12–18% reduction in cardiovascular event risk in observational cohorts. Tarragon-specific rutin content and its clinical contribution to the herb's antidiabetic profile have not been isolated in clinical trials.

Found In 2 Herbs

3D Molecular Structure

Flavonol glycoside
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Rutin (Quercetin-3-O-rutinoside)

Flavonol glycosideSugar-bound molecules that control drug release in the body

Representative pattern: C₁₅H₁₀O₃

Atoms
Carbon
Oxygen

Related Compounds (Flavonol glycoside)

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These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. This content is for educational purposes only and is not a substitute for professional medical advice.