# Melinjo-derived Gnetin C restores metabolic balance via dual adipose and hepatic effects in high-fat diet mice

**Authors:** Tomoki Kishimoto, Aoi Nasu, Mai Uemura, Keisuke Kawano, Choyo Ogasawara, Ayami Fukuyama, Hirofumi Nohara, Ryunosuke Nakashima, Noriki Takahashi, Yukio Fujiwara, Tomoki Ikuta, Mary Ann Suico, Hirofumi Kai, Tsuyoshi Shuto

PMC · DOI: 10.1038/s41598-025-25705-x · 2025-11-25

## TL;DR

Gnetin C, a compound from Melinjo seeds, improves metabolic health in obese mice by acting on both fat and liver tissues.

## Contribution

Gnetin C is identified as a dual-acting compound that restores metabolic balance through adipose and hepatic mechanisms.

## Key findings

- Gnetin C improves body weight and fasting glucose in high-fat diet-fed mice.
- It enhances adiponectin multimerization and suppresses fat accumulation via the PPARγ-DsbA-L axis.
- Gnetin C modulates hepatic Sirt1 and FGF21 signaling to improve metabolic outcomes.

## Abstract

Multi-organ regulation underlies metabolic health, especially in the context of adipose-liver dysfunction during obesity. Previous findings identified Melinjo seed extract (MSE) as a promising modulator of metabolic disorders, although its active component remained unknown. Gnetin C, a trans-resveratrol dimer from MSE, likely serves as the key factor, yet its direct metabolic role remains unclear. Here, Gnetin C was administered to high-fat diet (HFD)-fed mice, which significantly improved body weight and fasting glucose, attributed to enhanced adiponectin (APN) multimerization. In adipose tissue, Gnetin C directly promotes APN multimerization and suppresses fat accumulation by up-regulating the PPARγ-DsbA-L axis, while concurrently modulating hepatic Sirt1, which may contribute to increased FGF21 production. This paracrine FGF21 signaling, suggested by elevated Fgfr1 in hepatocytes and βKlotho in adipocytes, further augments APN multimerization. These findings underscore the importance of a multi-tissue approach to obesity management and position Gnetin C as an integrative therapeutic candidate, restoring metabolic balance via dual adipose and hepatic effects in HFD mice.

The online version contains supplementary material available at 10.1038/s41598-025-25705-x.

## Linked entities

- **Genes:** ANPEP (alanyl aminopeptidase, membrane) [NCBI Gene 290], PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468], Gstk1 (glutathione S-transferase kappa 1) [NCBI Gene 76263], SIRT1 (sirtuin 1) [NCBI Gene 23411], FGF21 (fibroblast growth factor 21) [NCBI Gene 26291], FGFR1 (fibroblast growth factor receptor 1) [NCBI Gene 2260]
- **Chemicals:** Gnetin C (PubChem CID 21633857), trans-resveratrol (PubChem CID 445154)
- **Diseases:** obesity (MONDO:0011122)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Fgfr1 (fibroblast growth factor receptor 1) [NCBI Gene 14182] {aka Eask, FGFR-I, FLG, Fgfr-1, Flt-2, Fr1}, Pparg (peroxisome proliferator activated receptor gamma) [NCBI Gene 19016] {aka Nr1c3, PPAR-gamma, PPAR-gamma2, PPARgamma, PPARgamma2}, Adipoq (adiponectin, C1Q and collagen domain containing) [NCBI Gene 11450] {aka 30kDa, APN, Acdc, Acrp30, Ad, Adid}, Gstk1 (glutathione S-transferase kappa 1) [NCBI Gene 76263] {aka 0610025I19Rik, DsbA-L}, Fgf21 (fibroblast growth factor 21) [NCBI Gene 56636] {aka Fgf8c}, Sirt1 (sirtuin 1) [NCBI Gene 93759] {aka SIR2L1, Sir2, Sir2a, Sir2alpha}, Klb (klotho beta) [NCBI Gene 83379] {aka betaKlotho}
- **Diseases:** adipose-liver dysfunction (MESH:D017093), metabolic disorders (MESH:D008659), obesity (MESH:D009765)
- **Chemicals:** MSE (-), trans-resveratrol (MESH:D000077185), Gnetin C (MESH:C575740), glucose (MESH:D005947)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12647683/full.md

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Source: https://tomesphere.com/paper/PMC12647683