# Purification and Anti-Inflammatory Activity of Walnut Exosome-like Nanoparticles

**Authors:** Shuo Zhang, Xinhui Wang, Shijie Zhu, Zhou Chen, Siting Li, Aijin Ma, Yingmin Jia, Junxia Xia, Bing Qi

PMC · DOI: 10.3390/foods15050870 · Foods · 2026-03-04

## TL;DR

Researchers isolated walnut-derived exosome-like nanoparticles and found they reduce inflammation and oxidative stress in cells.

## Contribution

First isolation and characterization of walnut exosome-like nanoparticles with demonstrated anti-inflammatory and antioxidant effects.

## Key findings

- Walnut exosome-like nanoparticles (WELNs) reduced oxidative stress and inflammation in macrophages.
- WELNs suppressed pro-inflammatory cytokines and inhibited the MAPK signaling pathway.
- WELNs showed no cytotoxicity and had antioxidant enzyme-boosting properties.

## Abstract

This study reports the first successful isolation and characterization of exosome-like nanoparticles from walnut kernels (WELNs). The isolated WELNs exhibited a typical cup-shaped morphology with an average diameter of 139.7 ± 67.5 nm, a concentration of 7.4 × 1011 particles/mL, and a zeta potential of −17.47 ± 4.06 mV. Proteomic and small RNA sequencing analyses confirmed the presence of diverse proteins and microRNAs within WELNs. In vitro assays demonstrated their potent antioxidant capacity, with radical scavenging rates of 67.54% against ABTS+ and 48.59% against DPPH+ at 102 μg/mL and IC50 values of 89.7 μg/mL and >102 μg/mL for scavenging of ABTS+ and DPPH+ radicals, respectively. Cytotoxicity assays indicated no adverse effects on RAW264.7 macrophage viability at concentrations up to 60 μg/mL. In LPS-stimulated RAW264.7 macrophages, WELN treatment (20–60 μg/mL) dose-dependently mitigated oxidative stress by reducing intracellular ROS levels (down to 81.22% of the control at 60 μg/mL) and malondialdehyde (MDA) content while restoring the activities of antioxidant enzymes catalase (CAT) and superoxide dismutase (SOD). Furthermore, WELNs significantly suppressed the production of nitric oxide (NO) and pro-inflammatory cytokines TNF-α, IL-6, and IL-1β (reduced to approximately 30.8%, 22.7%, and 23.6% of LPS-induced levels, respectively, at 60 μg/mL). Mechanistic investigation revealed that the anti-inflammatory effect was mediated through the inhibition of the MAPK signaling pathway, as evidenced by decreased phosphorylation of p38, ERK, and JNK. In conclusion, WELNs exhibit dual anti-inflammatory and antioxidant properties. This study provides the first evidence of bioactivity for walnut-derived exosome-like nanoparticles, advancing the mechanistic understanding of walnuts’ health benefits and highlighting their potential as a natural component for functional food applications.

## Linked entities

- **Proteins:** Cat (Catalase), CRK (CRK proto-oncogene, adaptor protein), EPHB2 (EPH receptor B2), MAPK8 (mitogen-activated protein kinase 8)
- **Chemicals:** ABTS+ (PubChem CID 35688), nitric oxide (PubChem CID 145068), malondialdehyde (PubChem CID 10964)

## Full-text entities

- **Genes:** MAPK14 (mitogen-activated protein kinase 14) [NCBI Gene 1432] {aka CSBP, CSBP1, CSBP2, CSPB1, EXIP, Mxi2}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, CAT (catalase) [NCBI Gene 847], IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, MAPK8 (mitogen-activated protein kinase 8) [NCBI Gene 5599] {aka JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8}
- **Diseases:** Inflammatory (MESH:D007249), Cytotoxicity (MESH:D064420)
- **Chemicals:** ABTS+ (MESH:C002502), DPPH+ (MESH:C004931), LPS (MESH:D008070), MDA (MESH:D008315), ROS (-), NO (MESH:D009569)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12985304/full.md

## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12985304/full.md

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Source: https://tomesphere.com/paper/PMC12985304