Hermetica Superfood Encyclopedia
Legacy index-continuity record: the score and narrative are provisional and must not be represented as validated or human-approved.
Review flags: AWAITING_SEMANTIC_VALIDATION
Da Qing Ye (Isatis indigotica leaf) contains indirubin and isatin compounds that inhibit viral replication and modulate immune responses. This traditional Chinese herb demonstrates antiviral activity against influenza and respiratory infections through interference with viral RNA synthesis.
Reported Benefits (Provisional)
Origin & History
Da Qing Ye is obtained from the leaves of the Isatis indigotica plant. It is traditionally dried and used in herbal formulations.
Research Narrative (Provisional)
Studies suggest that Da Qing Ye may have antiviral properties, with some evidence supporting its use in treating viral infections. However, more clinical trials are needed.
Preparation & Dosage
Dosage guidance is withheld because the publication gate has not recorded adequate support for this profile.
Nutritional Profile
Da Qing Ye (Isatis indigotica leaf) is a medicinal herb rather than a dietary staple, so macronutrient content is minimal in therapeutic doses. Bioactive compounds dominate its profile: Indole alkaloids are the primary constituents, including indigo (indigotin) at approximately 0.2–0.8% dry weight and indirubin at 0.01–0.05% dry weight, both responsible for antiviral and anti-inflammatory activity. Isatin is present at trace levels (~0.01% dry weight) contributing to antimicrobial effects. Tryptanthrin is found at approximately 0.02–0.1% dry weight with notable anti-inflammatory and immunomodulatory properties. Sinigrin (a glucosinolate) is present at approximately 0.5–1.2% dry weight and hydrolyzes to allyl isothiocyanate upon processing, contributing to antibacterial effects. Epigoitrin (a glucosinolate derivative) is present at 0.1–0.3% dry weight and is considered a key antiviral marker compound. Flavonoids including quercetin and kaempferol glycosides are present at approximately 0.3–0.6% dry weight, supporting antioxidant activity. Polysaccharides account for approximately 3–8% dry weight and are primary immunostimulatory agents boosting lymphocyte production. Organic acids including succinic acid and salicylic acid are present at trace to low concentrations (~0.1–0.5% dry weight). Amino acids including arginine and glutamic acid are present in small amounts (~1–3% dry weight of crude herb). Trace minerals include potassium (~800–1200 mg/100g dry), calcium (~400–600 mg/100g dry), magnesium (~150–250 mg/100g dry), and iron (~15–30 mg/100g dry). Vitamin C is present at approximately 50–120 mg/100g fresh weight but degrades significantly upon drying or decoction. Bioavailability notes: Indirubin and indigo have low oral bioavailability (~10–20%) due to poor water solubility but are enhanced by alcohol extraction or enteric formulations. Polysaccharides are water-soluble and readily extracted in traditional decoctions, offering high bioavailability in that preparation. Epigoitrin is relatively heat-stable and water-soluble, making it well-extracted in standard decoctions. Sinigrin bioavailability is reduced upon prolonged boiling due to thermal degradation of myrosinase enzyme needed for activation.
Reported Mechanism (Provisional)
Da Qing Ye's primary bioactive compounds indirubin and isatin inhibit viral RNA polymerase and neuraminidase enzymes, preventing viral replication. The herb modulates cytokine production by suppressing pro-inflammatory IL-6 and TNF-α while enhancing interferon-γ production. Indole alkaloids in the leaf activate T-helper cells and increase natural killer cell activity through NF-κB pathway regulation.
Clinical Narrative (Provisional)
Human studies on Da Qing Ye are limited, with most evidence from in vitro and animal research. Laboratory studies show 70-85% inhibition of influenza A virus at 100-200 μg/mL concentrations. Animal trials with 1-2 g/kg doses demonstrated reduced viral load and inflammatory markers in respiratory infections. Clinical evidence remains preliminary, requiring larger human trials to establish therapeutic efficacy and optimal dosing protocols.
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