# Neuroprotective effects of kojic acid and nano-kojic acid in experimental brain ischemia induced by bilateral common carotid artery occlusion

**Authors:** Mohammad Shokati Sayyad, Majid Saeedi, Fatemeh Shaki, Fereshteh Talebpour Amiri, Reza Negarandeh, Mohammad Seyedabadi

PMC · DOI: 10.22038/ijbms.2025.89790.19367 · Iranian Journal of Basic Medical Sciences · 2026-01-01

## TL;DR

This study shows that nano-kojic acid improves brain protection in a rat model of brain ischemia better than regular kojic acid.

## Contribution

The novel contribution is the evaluation of nanostructured kojic acid's enhanced neuroprotective effects in cerebral ischemia.

## Key findings

- Nano-kojic acid significantly improved behavioral outcomes in ischemic rats.
- Both KA and nKA reduced oxidative stress and inflammation markers in brain tissue.
- Nano-kojic acid increased Nrf2 expression and reduced IL-6 compared to KA.

## Abstract

Brain ischemia remains a leading cause of death and neurological disability worldwide, with current treatments limited by narrow therapeutic windows and insufficient neuroprotection. Kojic acid (KA), a natural compound with demonstrated anti-oxidant and anti-inflammatory properties, has not been thoroughly evaluated in cerebral ischemia. Its limited brain bioavailability may have hindered the identification of its potential therapeutic effects. This study aimed to investigate the effects of both KA and its nanostructured lipid carriers (nKA) in a rat bilateral common carotid artery occlusion (BCCAO) model.

Adult male rats were randomly allocated to seven groups: sham, BCCAO, KA (1 and 10 mg/kg), nKA (1 and 10 mg/kg), and vehicle. Following BCCAO surgery, animals received intraperitoneal treatments for seven days. Behavioral assessments included the modified neurological severity score and grid walk test. Brain and serum samples were collected to evaluate histopathology, gene expression, oxidative stress markers, inflammatory cytokines, and pharmacokinetic parameters.

Histological analysis indicated reduced neuronal loss in both KA and nKA-treated groups. Notably, only nKA significantly improved behavioral outcomes. Both treatments reduced the pro-apoptotic gene BAX and the pro-inflammatory cytokine TNF-α, while nKA additionally increased Nrf2 and reduced IL-6 expression. Both formulations mitigated oxidative stress by decreasing reactive oxygen species, protein carbonylation, and malondialdehyde levels, while also increasing glutathione concentrations.

Nano-kojic acid showed better neurobehavioral improvements, while both forms reduced oxidative stress and inflammation, indicating neuroprotective potential. Further studies are needed to clarify mechanisms and long-term safety.

## Linked entities

- **Genes:** BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581], GABPA (GA binding protein transcription factor subunit alpha) [NCBI Gene 2551], TNF (tumor necrosis factor) [NCBI Gene 7124], IL6 (interleukin 6) [NCBI Gene 3569]
- **Chemicals:** kojic acid (PubChem CID 3840), glutathione (PubChem CID 124886), malondialdehyde (PubChem CID 10964)
- **Diseases:** brain ischemia (MONDO:0005299)
- **Species:** Rattus norvegicus (taxon 10116), Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, nKA [NCBI Gene 326405], Il6 (interleukin 6) [NCBI Gene 24498] {aka ILg6, Ifnb2}, Bax (BCL2 associated X, apoptosis regulator) [NCBI Gene 24887], Nfe2l2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 83619]
- **Diseases:** neuronal loss (MESH:D009410), neurological disability (MESH:D009069), Brain ischemia (MESH:D002545), BCCAO (MESH:D002340), inflammation (MESH:D007249), death (MESH:D003643)
- **Chemicals:** glutathione (MESH:D005978), lipid (MESH:D008055), KA (MESH:C011890), malondialdehyde (MESH:D008315), reactive oxygen species (MESH:D017382)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12867113/full.md

## References

60 references — full list in the complete paper: https://tomesphere.com/paper/PMC12867113/full.md

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Source: https://tomesphere.com/paper/PMC12867113