
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
Kaim Leaf (Mitragyna parvifolia) is rich in alkaloids (including mitragynine at 38.61–39.79 mg/g dry weight), flavonoids, and triterpenoids that confer documented anti-inflammatory, analgesic, antimicrobial, and wound-healing properties. In hepatocyte cell models, its primary alkaloid mitragynine upregulates LDL receptor (LDLR) protein expression by 2.19-fold and reduces PCSK9 protein to 0.30-fold, suggesting a role in cholesterol metabolism modulation, though hepatotoxic potential at high doses warrants caution.

Reported Benefits (Provisional)
Origin & History

Kaim Leaf, derived from Mitragyna parvifolia, is a botanical native to India, Sri Lanka, and Bangladesh. This tree thrives in various regions across South Asia and is recognized for its traditional medicinal applications in wound healing and anti-inflammatory support.
Research Narrative (Provisional)
Research on Mitragyna parvifolia has documented a rich phytochemical profile including alkaloids (mitragynine, dihydrocorynantheine), flavonoids, glycosides, and triterpenoids, confirmed through HPLC and GC-MS analyses. In vitro studies using HepG2 hepatocyte models demonstrated that mitragynine at 0.25 mg/ml upregulates LDLR expression by 2.19-fold and boosts cell-surface LDLR by 229.9%, while simultaneously downregulating PCSK9 via SREBP-2 and HNF-1α suppression. Ethnobotanical and ethnomedicinal reviews across Indian traditional medicine systems—including Ayurveda, Siddha, and tribal medicine—have consistently documented Kaim Leaf's applications for fever, pain, inflammation, skin infections, and wound healing. A ScienceDirect-indexed study specifically investigated the anti-inflammatory potential of Mitragyna parvifolia, identifying bioactive fractions that inhibit pro-inflammatory mediators in both in vitro and in vivo models.
Preparation & Dosage
Dosage guidance is withheld because the publication gate has not recorded adequate support for this profile.
Nutritional Profile
- Alkaloids - Tannins - Flavonoids - Saponins - Triterpenoids
Reported Mechanism (Provisional)
Mitragynine, the principal indole alkaloid in Kaim Leaf, modulates cholesterol homeostasis by increasing LDL receptor (LDLR) protein expression approximately 2.19-fold and enhancing cell-surface LDLR levels by 229.9% in HepG2 cells, while concurrently reducing PCSK9 protein expression to 0.30-fold through downregulation of transcription factors SREBP-2 and HNF-1α. Its anti-inflammatory activity is attributed to the suppression of key pro-inflammatory mediators including cyclooxygenase-2 (COX-2), tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6), and nuclear factor kappa-B (NF-κB) signaling pathways. The analgesic properties are believed to involve opioid receptor modulation, particularly partial agonism at mu-opioid receptors, consistent with the pharmacology of structurally related corynanthean-type alkaloids. Additional flavonoids and triterpenoids present in the leaf contribute synergistic antioxidant effects by scavenging reactive oxygen species (ROS) and enhancing endogenous antioxidant enzyme activity (SOD, catalase, glutathione peroxidase).
Clinical Narrative (Provisional)
Current evidence is limited to preclinical studies with no randomized controlled human trials available. In vitro studies using HepG2 cells demonstrated significant cholesterol-modulating effects at 0.25 mg/ml extract concentrations. A 28-day rat toxicity study (10-150 mg/kg body weight) revealed hepatic and renal damage with elevated liver enzymes. One unspecified clinical study reported good tolerability and low abuse potential, but lacks detailed methodology and sample size data.
Also Known As
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