A study to determine the effect of nano-selenium and thymoquinone on the Nrf2 gene expression in Alzheimer's disease
- PMID: 39887156
- PMCID: PMC11792829
- DOI: 10.1080/20565623.2025.2458434
A study to determine the effect of nano-selenium and thymoquinone on the Nrf2 gene expression in Alzheimer's disease
Abstract
Introduction: Alzheimer's disease is a developing public health concern in aging communities that affects a sizable section of the global population. The risk of Alzheimer's disease increases with age; it affects one-third of males and two-thirds of women. This research attempts to assess the effect of nano-selenium and thymoquinone on Nrf2 gene expression levels in Alzheimer's disease (AD).
Methods: There were five identical groups of 50 albino male rats: a control group that was healthy; an AD positive control group; an AD group that received nano-selenium (5 mg/kg); an AD group that received thymoquinone (2 mg/kg); and an AD group that received both. The duration of treatment was 4 weeks. The levels of Nrf2 in brain tissues were evaluated using real-time PCR.
Results: Nrf2 mean expression levels in the nano-selenium-treated rats, the thymoquinone-treated rats, and the rats that were given both treatments all increased significantly compared to AD rats with no treatment.
Conclusions: This study showed that nano-selenium and thymoquinone elevated Nrf2 gene expression levels in AD.
Keywords: Alzheimer’s disease; antioxidant; lipopolysaccharides; nano-selenium; neurodegeneration; neuroprotective; nigella sativa; thymoquinone.
Plain language summary
Alzheimer’s disease (AD) is a common dementia causing cognitive decline. Nrf2 signaling may be a potential therapeutic target, while thymoquinone and nano-selenium could be effective neuroprotective agents for AD management, potentially reducing neuronal damage. In this study, the effects of thymoquinone and nano-selenium treatments on AD rat models were evaluated through behavior study by performing the Morris Water Maze test, estimation of different markers (Nrf2, Aβ-42, GSH, MDA, and TNF-α), and histopathological examination of brain tissue.
Conflict of interest statement
The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.
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