# Maackiain Reduces Neuroinflammation by Modulating Inflammatory Signals in LPS-Induced In Vitro and In Vivo Models

**Authors:** Tianchan Yun, Yue Xiao, Yanmei Gong, Yanxian Lai, Shiya Huang, Yanqing Ma, Yixi Zeng, Lanyue Zhang, Cong Deng

PMC · DOI: 10.4014/jmb.2508.08046 · Journal of Microbiology and Biotechnology · 2026-02-05

## TL;DR

Maackiain reduces brain inflammation in lab and animal models, showing promise as a treatment for neurological diseases.

## Contribution

The study demonstrates MAA's anti-neuroinflammatory effects through in vitro and in vivo experiments.

## Key findings

- Maackiain improved cell viability and reduced NO, ROS, and Fe2+ in LPS-treated BV2 cells.
- In mice, MAA improved memory and reduced IBA-1, COX-2, and IL-6 in brain regions.
- Higher MAA concentrations showed stronger anti-inflammatory effects in both models.

## Abstract

Neuroinflammation, an immune process in the central nervous system (CNS), is a key contributor to a range of neurological diseases, including neurodegenerative disorders (e.g., Alzheimer’s and Parkinson’s disease), stroke, and depression, underscoring its significant pathological relevance. While maackiain (MAA) exhibits potent anti-inflammatory activity, its potential to mitigate neuroinflammation remains poorly understood. This study investigated the therapeutic effects of MAA on lipopolysaccharide (LPS)-induced neuroinflammation and its underlying mechanisms. In vitro, MAA significantly improved BV2 cell viability and reduced nitric oxide (NO) expression in LPS-treated cells, decreased the expression of reactive oxygen species (ROS), and it also inhibited the accumulation of Ferrous ion (Fe2+) and lipid peroxides as well as the damage to mitochondria. Higher concentrations of MAA were more effective, consistent with subsequent animal experiments. In vivo, mice treated with MAA showed improved memory in the Morris water maze compared to the LPS group. Nissl staining revealed fewer IBA-1 positive cells and a decrease in COX-2 and IL-6 levels in the hippocampus and cortex. This compound also increased the number of normal neurons in the cortex and CA3 region. The results of this study highlight the inhibitory effects of MAA on neuroinflammation, suggesting its potential as an effective therapeutic agent for treating neuroinflammation.

## Linked entities

- **Proteins:** COX2 (cytochrome c oxidase subunit II), IL6 (interleukin 6), AIF1 (allograft inflammatory factor 1)
- **Chemicals:** maackiain (PubChem CID 91510), nitric oxide (PubChem CID 145068), Ferrous ion (PubChem CID 27284)
- **Diseases:** Alzheimer’s disease (MONDO:0004975), Parkinson’s disease (MONDO:0005180), stroke (MONDO:0005098), depression (MONDO:0002050)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Iba1 (induction of brown adipocytes 1) [NCBI Gene 114737], COX2 (cytochrome c oxidase subunit II) [NCBI Gene 17709], Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}
- **Diseases:** depression (MESH:D003866), Alzheimer's and Parkinson's disease (MESH:D010300), Inflammatory (MESH:D007249), Neuroinflammation (MESH:D000090862), neurodegenerative disorders (MESH:D019636), stroke (MESH:D020521), neurological diseases (MESH:D020271)
- **Chemicals:** ROS (MESH:D017382), lipid peroxides (MESH:D008054), LPS (MESH:D008070), MAA (MESH:C001449), Fe2+ (-), NO (MESH:D009569)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

14 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12883318/full.md

## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC12883318/full.md

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Source: https://tomesphere.com/paper/PMC12883318