# Related Mechanism of Limonene Improves LPS-Induced Neuroinflammation

**Authors:** Yingjuan Jiang, Geng Liu, Qingqing Liu, Lanyue Zhang, Yanping Tan, Junlin Cen, Yan Zhao, Aiguo Li

PMC · DOI: 10.4014/jmb.2411.11053 · Journal of Microbiology and Biotechnology · 2025-05-28

## TL;DR

This study shows that limonene, a compound from citrus oils, reduces neuroinflammation in mice by suppressing immune cell activation and improving memory and learning.

## Contribution

The study identifies limonene's novel anti-neuroinflammatory mechanism through transcriptomic and cellular analyses in an LPS-induced mouse model.

## Key findings

- Limonene reduced LPS-induced neuroinflammation by lowering GFAP and IBA-1 levels in mice.
- Limonene improved spatial memory and learning and reduced neuronal death in the hippocampus and cerebral cortex.
- Transcriptomic analysis showed limonene modulates inflammatory and immune signaling pathways.

## Abstract

Limonene, a component of volatile oils extracted from citrus plants, is known traditionally to treat inflammation. However, the anti-neuroinflammation efficacy and mechanism remain unclear. In this study, lipopolysaccharide was used as a neuroinflammatory inducer to investigate the mechanism of limonene in combating neuroinflammation in mice. Gas chromatography-mass spectrometry (GCMS) was used to identify the main components of Citrus sinensis (L.) Osbeck essential oil. A total of 21 compounds were identified in Citrus sinensis (L.) Osbeck essential oil, of which limonene, myrcene, and carene were the main components. Limonene was found to reduce LPS-induced neuroinflammatory responses in mice, as evidenced by decreased glial fibrillary acidic protein (GFAP) and ionized calcium-binding adapter molecule 1 (IBA-1) levels, along with suppressed expression of inflammatory cytokines. In addition, limonene improved the spatial memory and learning ability of mice caused by neuroinflammation, as well as neuronal death in the cerebral cortex and hippocampus. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) results showed that limonene had no obvious toxicity to BV2 cells when the concentration was 4 mg/ml. Transcriptomic analysis revealed the effects of limonene on inflammatory response, immune regulation, and other signaling pathways. These results reveal that limonene may improve LPS-induced neuroinflammation by regulating microglia and astrocyte activation and inflammatory response and may be used as a drug for the treatment of neuroinflammation in the future.

## Linked entities

- **Proteins:** GFAP (glial fibrillary acidic protein), AIF1 (allograft inflammatory factor 1)
- **Chemicals:** limonene (PubChem CID 22311), myrcene (PubChem CID 31253), carene (PubChem CID 26049), 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (PubChem CID 64965)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Aif1 (allograft inflammatory factor 1) [NCBI Gene 11629] {aka AIF-1, D17H6S50E, G1, Iba1}, Gfap (glial fibrillary acidic protein) [NCBI Gene 14580]
- **Diseases:** neuronal death (MESH:D009410), toxicity (MESH:D064420), inflammation (MESH:D007249), Neuroinflammation (MESH:D000090862)
- **Chemicals:** 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MESH:C022616), volatile oils (MESH:D009822), L. (MESH:D007930), Osbeck essential oil (-), LPS (MESH:D008070), myrcene (MESH:C509595), Limonene (MESH:D000077222), MTT (MESH:C070243)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Citrus sinensis (apfelsine, species) [taxon 2711]
- **Cell lines:** BV2 — Mus musculus (Mouse), Transformed cell line (CVCL_0182)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12149406/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12149406/full.md

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Source: https://tomesphere.com/paper/PMC12149406