2. Academic Validation
  3. Anacardic acid improves neurological deficits in traumatic brain injury by anti-ferroptosis and anti-inflammation

Anacardic acid improves neurological deficits in traumatic brain injury by anti-ferroptosis and anti-inflammation

  • Exp Neurol. 2023 Oct 9:370:114568. doi: 10.1016/j.expneurol.2023.114568.
Yu Liu 1,  Zongren Zhao 2,  Jianqiang Guo 1,  Yuanhao Ma 1,  Jing Li 2,  Huanhuan Ji 2,  Zhongjun Chen 2,  Jinyu Zheng 3
Affiliations

Affiliations

  • 1 Department of Neurosurgery, The Affiliated Huai'an Hospital of Xuzhou Medical University, Huai'an 223022, China; Xuzhou Medical University, Xuzhou 221000, China.
  • 2 Department of Neurosurgery, The Affiliated Huai'an Hospital of Xuzhou Medical University, Huai'an 223022, China.
  • 3 Department of Neurosurgery, The Affiliated Huai'an Hospital of Xuzhou Medical University, Huai'an 223022, China. Electronic address: [email protected].
PMID: 37820939 DOI: 10.1016/j.expneurol.2023.114568
Abstract

Background: Traumatic brain injury (TBI) is an important cause of disability and death. TBI leads to multiple forms of nerve cell death including Ferroptosis due to iron-dependent lipid peroxidation. Anacardic acid (AA) is a natural component extracted from cashew nut shells, which has been reported to have neuroprotective effects in traumatic brain injury. We investigated whether AA has an anti-ferroptosis effect in TBI.

Methods: We used the Feeney free-fall impact method to construct a TBI model to investigate the effect of AA on Ferroptosis caused by TBI, in which Ferrostatin-1 (Fer-1), a Ferroptosis inhibitor, served as a positive control group. We first identified the therapeutic effect of AA on TBI through modified neurological severity score (mNSS) and determined the appropriate concentration. Secondly, we investigated the effect of AA on the expression level of the key protein of Ferroptosis by Western blotting and immunohistochemistry. Then the effect of AA on nerve tissue injury and nerve function improvement was verified. Finally, enzym-linked immunosorbent assay (ELISA) was used to verify that AA could reduce inflammation after TBI.

Results: We found the intensely inhibitory effect of AA on Ferroptosis, which is in parallel with the results obtained after Fer-1 treatment. In addition, AA and Fer-1 mitigated TBI-mediated tissue defects, destruction of the blood-brain barrier, and neurodegeneration. Novel object recognition (NOR), mNSS and water maze test showed that AA could significantly reduce the impairment of neural function and behavioral cognitive ability caused by TBI. Finally, we also demonstrated that AA has not only an anti-ferroptosis effect, but also an anti-inflammation effect.

Conclusions: AA can reduce the neurological impairment and behavioral cognitive impairment caused by TBI through the dual effect of anti-ferroptosis and anti-inflammation.

Keywords

Anacardic acid; Ferroptosis; Inflammation; Neuroprotection; Traumatic brain injury.

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