# Cosmeceutical Potential of Mitragyna speciosa (Kratom): Anti-Adipogenic and Antioxidant Properties of Extracts and Mitragynine

**Authors:** Sudthiworarak Kaewchompoo, Prapapan Temkitthawon, Kalyarut Phumlek, Neti Waranuch, Ngamrayu Ngamdokmai, Kornkanok Ingkaninan

PMC · DOI: 10.3390/molecules30214256 · 2025-10-31

## TL;DR

This study explores Kratom's potential as a cosmeceutical by showing its extracts and mitragynine can reduce fat and act as antioxidants.

## Contribution

The study identifies mitragynine as the key anti-adipogenic compound in Kratom extracts for cosmeceutical use.

## Key findings

- Kratom extracts and mitragynine significantly inhibited lipid accumulation in 3T3-L1 adipocytes by up to 50–70%.
- Phenolic constituents in Kratom extracts showed antioxidant activity comparable to ascorbic acid in DPPH, ABTS, and FRAP assays.

## Abstract

Kratom (Mitragyna speciosa (Korth.) Havil.) is a medicinal plant containing bioactive alkaloids, notably mitragynine and 7-hydroxymitragynine, which are psychoactive compounds with analgesic and stimulant properties. Due to safety concerns, the use of Kratom leaves and mitragynine in oral pharmaceutical products is restricted. Therefore, their potential as topical cosmeceutical agents merits further exploration. This study aimed to investigate the antioxidant and anti-adipogenic activities of Kratom ethanolic (Et-MS) and alkaloid-rich (Alk-MS) extracts, as well as purified mitragynine, to determine whether mitragynine is the major bioactive compound responsible for lipid reduction in 3T3-L1 adipocytes. The antioxidant properties were assessed using DPPH, ABTS, and FRAP assays, yielding EC50 values of 0.06 mg/mL, 0.29 mg/mL, and 55 g Fe2+/100 g for Et-MS, respectively. In comparison, ascorbic acid (positive control) showed a DPPH EC50 value of 0.002 mg/mL. Both Alk-MS and mitragynine significantly inhibited lipid accumulation in 3T3-L1 adipocytes by up to 50–70% at non-cytotoxic concentrations (≤25 µg/mL), as determined by Oil Red O staining. These findings provide preliminary in vitro evidence that phenolic constituents contribute to antioxidant capacity, while mitragynine is the principal anti-adipogenic constituent in Kratom extracts. Collectively, the results support the potential for further development of Kratom-derived extracts and mitragynine as plant-based candidates for topical or cosmeceutical applications targeting subcutaneous fat and oxidative skin damage.

## Linked entities

- **Chemicals:** mitragynine (PubChem CID 3034396), 7-hydroxymitragynine (PubChem CID 44301524), ascorbic acid (PubChem CID 9888239)

## Full-text entities

- **Diseases:** skin (MESH:D012871)
- **Chemicals:** lipid (MESH:D008055), alkaloid (MESH:D000470), 7-hydroxymitragynine (MESH:C482678), ascorbic acid (MESH:D001205), Oil Red O (MESH:C011049), Et-MS (-), ABTS (MESH:C002502), Mitragynine (MESH:C001801), DPPH (MESH:C004931)
- **Species:** Mitragyna speciosa (kratom, species) [taxon 170351]
- **Cell lines:** 3T3-L1 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0123)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12608821/full.md

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Source: https://tomesphere.com/paper/PMC12608821