# Monoterpene-rich essential oil from Artemisia santonicum L. exerts neuroprotective effects in Aβ-induced SH-SY5Y cells: Modulation of tau pathology, neuroinflammation, oxidative stress, and synaptic-metabolic pathways

**Authors:** Serap Nigdelioglu Dolanbay

PMC · DOI: 10.1093/toxres/tfaf155 · Toxicology Research · 2025-11-12

## TL;DR

This study explores how an essential oil from Artemisia santonicum protects brain cells in Alzheimer's disease by targeting key disease mechanisms like inflammation and oxidative stress.

## Contribution

The study identifies and experimentally validates the neuroprotective effects of a monoterpene-rich essential oil from Artemisia santonicum against Alzheimer's pathology.

## Key findings

- The essential oil showed neuroprotective effects by reducing tau pathology and neuroinflammation in Aβ-induced SH-SY5Y cells.
- Monoterpenes modulated oxidative stress and synaptic-metabolic pathways in Alzheimer's disease models.
- Molecular docking and in vitro experiments confirmed the oil's potential to target key Alzheimer's-related proteins.

## Abstract

Understanding the complex biological mechanisms of ad requires innovative treatment approaches for this disease. In this context, natural compounds, especially monoterpenes, attract attention with their potential for biological activity. In this study, the therapeutic potential of monoterpene rich essential oil obtained from Artemisia santonicum L. for the treatment of ad was comprehensively evaluated. GC–MS analysis showed that the major monoterpenes were limonene, camphor, pinene, terpineol, and carvone in essential oil obtained from A. santonicum L. Possible common targets of monoterpenes with ad were predicted and their PPI networks were analyzed. Furthermore, gene set enrichment analysis was applied to understand the functional roles of these possible common targets and their relationships with biological pathways. Molecular docking studies revealed the binding affinities and interaction abilities of monoterpenes with the predicted possible common targets. The monoterpene rich essential oil obtained from A. santonicum L. used in our study provides a neuroprotective effect by targeting the pathological mechanisms of ad. We designed in vitro experiments to elucidate the mechanism of the mentioned neuroprotective effect. Within the scope of the study, neuroprotective effect analyses were performed to evaluate cell viability rates and in vitro AChE enzyme activity, while the ELISA method was used to determine phosphorylated tau levels and to assess neuroinflammatory responses. In addition, apoptosis levels, MMP changes and intracellular ROS accumulation were examined by flow cytometry analyses. These comprehensive analyses aimed to reveal the molecular mechanisms of the neuroprotective effect of monoterpene rich essential oil obtained from A. santonicum L. and to shed light on its potential therapeutic applications in ad.

## Linked entities

- **Proteins:** ab (abrupt), ACHE (acetylcholinesterase (Yt blood group)), MAPT (microtubule associated protein tau)
- **Chemicals:** limonene (PubChem CID 22311), camphor (PubChem CID 2537), pinene (PubChem CID 6654), terpineol (PubChem CID 17100), carvone (PubChem CID 7439)
- **Diseases:** Alzheimer's disease (MONDO:0004975)

## Full-text entities

- **Genes:** MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, ACHE (acetylcholinesterase (Yt blood group)) [NCBI Gene 43] {aka ACEE, ARACHE, N-ACHE, YT}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}
- **Diseases:** neuroinflammation (MESH:D000090862)
- **Chemicals:** ROS (-), limonene (MESH:D000077222), camphor (MESH:D002164), Monoterpene (MESH:D039821), essential oil (MESH:D009822), carvone (MESH:C006923)
- **Species:** Artemisia santonicum (species) [taxon 1287620]
- **Cell lines:** SH-SY5Y — Homo sapiens (Human), Neuroblastoma, Cancer cell line (CVCL_0019)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12608079/full.md

## References

107 references — full list in the complete paper: https://tomesphere.com/paper/PMC12608079/full.md

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Source: https://tomesphere.com/paper/PMC12608079