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Shikimic acid (SA) inhibits neuro-inflammation and exerts neuroprotective effects in an LPS-induced in vitro and in vivo model

Affiliation
Department of Radiation Oncology ,The First Hospital of Jilin University ,Changchun ,China
Bao, Xueying;
Affiliation
Department of Radiation Oncology ,The First Hospital of Jilin University ,Changchun ,China
Zheng, Zhuangzhuang;
Affiliation
Department of Radiation Oncology ,The First Hospital of Jilin University ,Changchun ,China
Lv, Jincai;
Affiliation
Department of Radiation Oncology ,The First Hospital of Jilin University ,Changchun ,China
Bao, Jindian;
Affiliation
Department of Radiation Oncology ,The First Hospital of Jilin University ,Changchun ,China
Chang, Sitong;
Affiliation
Department of Radiation Oncology ,The First Hospital of Jilin University ,Changchun ,China
Jiang, Xin;
Affiliation
Key Laboratory of Pathobiology ,Ministry of Education, and College of Basic Medical Science ,Jilin University ,Changchun ,China
Xin, Ying

Numerous studies have shown that neuroinflammation is involved in the process of neuronal damage in neurodegenerative diseases such as Parkinson’s disease (PD), for example, and that inhibiting neuroinflammation help improve PD. Shikimic acid (SA) has anti-inflammatory, analgesic and antioxidant activities in numerous diseases. However, its effect and mechanism in PD remain unclear. In this experiment, we found that SA inhibits production of pro-inflammatory mediators and ROS in LPS-induced BV2 cells. Mechanistic studies demonstrated that SA suppresses neuro-inflammation by activating the AKT/Nrf2 pathway and inhibiting the NF-κB pathway. Further in vivo study, we confirmed that SA ameliorated the neurological damage and behavioral deficits caused by LPS injection in mice. In summary, these study highlighted the beneficial role of SA as a novel therapy with potential PD drug by targeting neuro-inflammation.

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License Holder: Copyright © 2023 Bao, Zheng, Lv, Bao, Chang, Jiang and Xin.

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