
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
Salacia reticulata is an Ayurvedic herb containing salacinol and kotalanol compounds that inhibit alpha-glucosidase enzymes. These bioactive compounds help regulate blood sugar by slowing carbohydrate digestion and glucose absorption.

Origin & History

Salacia reticulata, known as Kothala himbutu, is a woody climber native to Sri Lanka and India, traditionally used in Ayurvedic medicine. The plant's stems, roots, and leaves are harvested and processed into extracts using water or ethanol extraction methods. The active components include polyphenols such as salacinol and kotalanol, which function as alpha-glucosidase inhibitors.
Research Narrative (Provisional)
Clinical evidence includes multiple randomized controlled trials, with a double-blind RCT (n=29) showing significant blood sugar reductions at 500mg/day for 6 weeks (PMID: 23767865). Additional trials demonstrated HbA1c reduction (PMIDs: 37885536, PMC10599346), improved postprandial glucose (PMID: 15707755), and enhanced immune function with microbiota changes (PMID: 26630568). A review noted consistent evidence over 6 weeks to 3 months for glucose and insulin improvements (PMID: 25889885).
Preparation & Dosage
Dosage guidance is withheld because the publication gate has not recorded adequate support for this profile.
Nutritional Profile
Salacia reticulata is not consumed as a bulk food ingredient but as a concentrated botanical extract; thus, macronutrient contribution is negligible at typical doses (500mg–1g/day). Key bioactive compounds drive its pharmacological profile: (1) Salacinol – a sulfonium sulfate cyclitol, primary alpha-glucosidase inhibitor, present at approximately 0.1–0.5% dry weight in root/stem bark; (2) Kotalanol – a structurally related thiosugar sulfonium compound, co-occurring with salacinol, present at ~0.05–0.2% dry weight, demonstrated to inhibit intestinal maltase and sucrase with IC50 values in the micromolar range; (3) Mangiferin – a C-glucosyl xanthone, present at ~0.3–1.2% dry weight in leaves, contributes antidiabetic and antioxidant activity via PPAR-gamma modulation; (4) Kotalagenin 16-acetate – a triterpenoid saponin involved in aldose reductase inhibition; (5) Mahanimbine and related alkaloids – minor constituents with lipase-inhibitory properties. Mineral content of crude root extract includes detectable calcium (~180–220 mg/100g dry extract), potassium (~300–400 mg/100g dry extract), and trace magnesium. Fiber content is present in whole plant preparations (~8–12% dry weight as insoluble fiber) but absent in standardized extracts. Bioavailability notes: Salacinol and kotalanol are polar, water-soluble compounds with limited passive intestinal absorption, which confines their primary activity to the intestinal lumen — this is mechanistically advantageous for postprandial glucose control but limits systemic bioavailability. Mangiferin exhibits moderate oral bioavailability (~20–30%) enhanced by food-matrix co-administration. Standardized commercial extracts are typically normalized to salacinol content (≥0.5%) or total alpha-glucosidase inhibitory activity.
Reported Mechanism (Provisional)
Salacia reticulata's primary compounds salacinol and kotalanol competitively inhibit alpha-glucosidase and alpha-amylase enzymes in the small intestine. This enzymatic inhibition slows the breakdown of complex carbohydrates into simple sugars, reducing postprandial glucose spikes. The compounds also appear to enhance insulin sensitivity through modulation of glucose transporter proteins.
Clinical Narrative (Provisional)
Clinical evidence shows 500mg daily of Salacia reticulata leaf extract significantly reduced fasting blood sugar in a 6-week trial of 29 participants. Extract-containing biscuits lowered HbA1c levels by 0.25% compared to placebo in diabetic patients. The existing studies are relatively small-scale, indicating promising but preliminary evidence for glucose management. More large-scale, long-term trials are needed to confirm therapeutic efficacy.
Also Known As
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