# Unveiling the Antihyperglycemic Potential of Arctium lappa L. (Asteraceae): Traditional Application, Phytochemistry, and Molecular Insights

**Authors:** Amangul A. Uzbekova, Kaldanay K. Kozhanova, Gulnara Kadyrbayeva, Bayan I. Tursubekova, Meruyert Amantayeva, Moldir A. Zhandabayeva, Meruyert I. Tleubayeva, Ahmet Beyatli

PMC · DOI: 10.3390/foods15040794 · 2026-02-23

## TL;DR

This review explores how Arctium lappa may help manage diabetes through its natural compounds and biological effects, though more human studies are needed.

## Contribution

The paper systematically reviews the antidiabetic mechanisms and bioactive compounds of Arctium lappa, highlighting gaps in clinical evidence.

## Key findings

- Arctium lappa's bioactives (arctigenin, arctiin, inulin) improve insulin sensitivity and lipid metabolism.
- Preclinical studies confirm antidiabetic effects via AMPK activation and insulin signaling modulation.
- Current evidence is limited to in vitro and animal models, with a lack of clinical trials in diabetic populations.

## Abstract

Diabetes mellitus is a chronic disease requiring multifunctional natural agents. Arctium lappa is traditionally used in Eastern and European medicine to address metabolic disorders. This comprehensive narrative review, conducted between 2000 and 2025 using international databases (Scopus, PubMed, Web of Science Core Collection, and Google Scholar), evaluates the species through its ethnomedicine, phytochemistry, preclinical evidence, and safety. The available evidence suggests that A. lappa exerts antidiabetic effects via multi-layered mechanisms, including AMPK activation, insulin signaling modulation, and increased GLUT4 translocation. Key bioactives (arctigenin, arctiin, and inulin) collectively improve insulin sensitivity and lipid metabolism. However, preclinical studies confirm these effects in animal models, while limited clinical data in non-diabetic cohorts focus on systemic inflammation. This highlights a significant gap in randomized controlled trials targeting glycemic control in diabetic populations. In this context, while A. lappa shows promise as a potential metabolic regulator; this evidence is currently derived primarily from in vitro and animal models. Systematic clinical trials are urgently required to establish glycemic efficacy in humans, validate its therapeutic potential, and determine the optimal dosage and safety profile. This review evaluates the multi-targeted biological potential of A. lappa to guide future research and evidence-based application.

## Linked entities

- **Proteins:** PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1), SLC2A4 (solute carrier family 2 member 4)
- **Chemicals:** arctigenin (PubChem CID 64981), arctiin (PubChem CID 100528)
- **Diseases:** Diabetes mellitus (MONDO:0005015)
- **Species:** Arctium lappa (taxon 4217)

## Full-text entities

- **Genes:** GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}
- **Diseases:** wasting-thirst syndrome (MESH:D019282), obesity (MESH:D009765), glycemia disorders (MESH:D009358), hypoglycemic (MESH:C000721848), metabolic disorders (MESH:D008659), gout (MESH:D006073), visual impairments (MESH:D014786), carbohydrate metabolism disorders (MESH:D002239), metabolic syndrome (MESH:D024821), hyperglycemia (MESH:D006943), chronic systemic inflammation (MESH:D007249), injury to (MESH:D014947), sugar disease (MESH:D004194), DM (MESH:D003920), liver lipotoxicity (MESH:D017093), allergies (MESH:D004342), insulin-deficient type 1-like diabetes (MESH:D003922), systemic (MESH:D015619), diabetic peripheral neuropathy (MESH:D010523), HED (MESH:D064386), type 2 DM (MESH:D003924), neuropathy (MESH:D009422), impaired glucose tolerance (MESH:D018149), abdominal obesity (MESH:D056128), eczema (MESH:D004485), diabetic complications (MESH:D048909), blood glucose dysregulation (MESH:D006402), insulin resistance (MESH:D007333), rheumatism (MESH:D012216), Toxicity (MESH:D064420), joint pain (MESH:D018771), polydipsia (MESH:D059606), diabetic retinopathy (MESH:D003930), chronic renal failure (MESH:D007676), hypoglycemia (MESH:D007003), cardiovascular complications (MESH:D002318)
- **Chemicals:** STZ (MESH:D013311), terpenes (MESH:D013729), biguanide (MESH:D001645), sulfonylureas (MESH:D013453), Phenolic acids (MESH:C017616), metformin (MESH:D008687), E (MESH:D004540), galactose (MESH:D005690), blood glucose (MESH:D001786), ethanol (MESH:D000431), inulin (MESH:D007444), aglycone (MESH:C458179), arctiin (MESH:C077992), lupeol (MESH:C010480), sulfate (MESH:D013431), glucuronide (MESH:D020719), arctigenin (MESH:C071942), rutin (MESH:D012431), thiazolidinedione (MESH:C089946), C (MESH:D002244), phytosterols (MESH:D010840), monosaccharides (MESH:D009005), Dicaffeoylquinic acid (MESH:C472707), triglyceride (MESH:D014280), sitosterol (MESH:C025473), quercetin (MESH:D011794), Polysaccharides (MESH:D011134), sterols (MESH:D013261), thiophene (MESH:D013876), lipid (MESH:D008055), arctigenic acid (MESH:C000596351), glutathione (MESH:D005978), CO2 (MESH:D002245), amyrin (MESH:C036380), ATP (MESH:D000255), AMP (MESH:D000249), SCFAs (MESH:D005232), Flavonoids (MESH:D005419), Chlorogenic acid (MESH:D002726), glucose (MESH:D005947), hydrogen (MESH:D006859), caffeic acid (MESH:C040048), luteolin (MESH:D047311), cynarin (MESH:C100257), oligosaccharides (MESH:D009844), sulfur (MESH:D013455), alloxan (MESH:D000496), D (MESH:D003903), A. lappa (-), acarbose (MESH:D020909), hydrocarbons (MESH:D006838), polyacetylenes (MESH:D000078789), carbohydrate (MESH:D002241), starch (MESH:D013213), triterpenes (MESH:D014315), Lignans (MESH:D017705), rhamnose (MESH:D012210)
- **Species:** Nigella sativa (black-caraway, species) [taxon 555479], Asarum minus (species) [taxon 76132], Zingiber officinale (ginger, species) [taxon 94328], Allium sativum (garlic, species) [taxon 4682], Arctium lappa (great burdock, species) [taxon 4217], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Trigonella foenum-graecum (fenugreek, species) [taxon 78534], Momordica charantia (balsam pear, species) [taxon 3673], Canis lupus familiaris (dog, subspecies) [taxon 9615], Hibiscus sabdariffa (red-sorrel, species) [taxon 183260], Curcuma longa (turmeric, species) [taxon 136217], Aloe vera (acibar, species) [taxon 34199], Homo sapiens (human, species) [taxon 9606], Bifidobacterium (genus) [taxon 1678], Rattus norvegicus (brown rat, species) [taxon 10116]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12939907/full.md

---
Source: https://tomesphere.com/paper/PMC12939907