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(1→3)(1→6)-Beta-D-Glucan (High Molecular Weight)

Moderate

Mechanism of Action

High-MW beta-glucans (100,000-200,000 Da) with (1→3) backbone and (1→6) side branches bind to complement receptor type 3 (CR3/CD11b/CD18) on macrophages and natural killer cells following C3 complement opsonization. This triggers NF-κB activation, TNF-α, IL-8, IL-1β, and IL-12 production, promoting Th1 immune response. Macrophage-produced IL-12 activates CD4+ T-cells and enhances CD8+ cytotoxic T-cell killing. Beta-glucan activity is strictly size-dependent — fragments below 100,000 Da are immunologically inactive, and (1→3) side branching is essential for receptor recognition.

Research Notes

In vivo studies using sarcoma 180 mouse models demonstrated 99-100% tumor inhibition with properly structured (1→3)(1→6)-beta-glucan fractions. The FIII-2-b fraction (43.4% protein, 50.2% carbohydrate) showed enhanced activity through protein-polysaccharide complex formation. An 8-week human study of 90 women showed 11.8% weight reduction and 11.0% cholesterol reduction with protein-bound polysaccharide fractions. A 16-week human safety study found no clinical abnormalities in blood, urine, or physical exams.

Found In 1 Herb

3D Molecular Structure

Polysaccharide (beta-glucan)
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(1→3)(1→6)-Beta-D-Glucan (High Molecular Weight)

Polysaccharide (beta-glucan)Complex carbohydrate polymers that modulate immune response

Representative pattern: (C₆H₁₀O₅)ₙ

Atoms
Carbon
Oxygen

Related Compounds (Polysaccharide (beta-glucan))

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