ArticleViewAbstractPharmacognosy Journal,2025,17,6,336-341.DOI:10.5530/pj.2025.17.104Published:December 2025Type:Original ArticleAntioxidant and Neuroprotective Potential of Ashwagandha In Aluminum-Induced ToxicityAnchana Babu, Rekha D Kini, Nayanatara Arun Kumar, Megha Gokul, Vandana Blossom, Sreerag P, and Shymala Nayak Anchana Babu1, Rekha D Kini1*, Nayanatara Arun Kumar1, Megha Gokul1, Vandana Blossom2, Sreerag P3, Shymala Nayak4 1Department of Physiology, Kasturba Medical College Mangalore, Manipal Academy of Higher Education, Manipal, INDIA. 2Department of Anatomy, Kasturba Medical College Mangalore, Manipal Academy of Higher Education, Manipal, INDIA. 3Department of Physiology, Srinivas Institute of Medical Sciences & Research Centre, Mukka, INDIA. 4Department of Biochemistry, Kasturba Medical College Mangalore, Manipal Academy of Higher Education, Manipal, INDIA. Abstract:Introduction : Aluminium is the most abundant metal and the third most common element in the Earth’s crust, following oxygen and silicon. Exposure to aluminium is associated with oxidative damage, primarily due to its ability to disrupt redox balance, generate reactive oxygen species, and impair antioxidant defense mechanisms.This study was aimed to find the potential role of ashwagandha on aluminium induced brain toxicity. Methods: In the present study rats were grouped into 4 groups of 6 rats in each. Brain tissue was removed and processed for biochemical and histopathological analysis. Results: In the present study, administration of aluminium to rats resulted in a significant decrease in tissue GSH levels and a corresponding increase in MDA levels in the aluminium-treated group compared to the normal control.. Treatment with Ashwagandha showed a significant increase in GSH level and decrease in MDA level. Photomicrographic sections of the Brain in Ashwagandha-treated rats showed normla neuronal Count and exposure to Aluminium has caused significant reduction in the neuronal count. Experimental group pretreated with ashwagandha showed a visible increase in neuronal count in different regions of the rat brain. Conclusion: The results revealed that oral administration of aluminium induced adverse oxidative effects in the exposed animals, while treatment with Ashwagandha markedly reduced the extent of aluminium chloride-induced brain injury. Keywords:Aluminum Chloride, Ashwagandha, Malondialdehyde, Oxidative stress, Reactive Oxygen Species, Reduced glutathioneView:PDF (325.69 KB) PDF Images Figure represents the Group 1& 2:AS group- dentate gyrus (150 x 150 sq μm2 area), the Cornu ammonis (300 sq μm length area - CA 1 to CA4) parts of the hippocampus, and Frontal Cortex ( 250 x 250 sq μm2 area FC) respectively ‹ Effect of Components of Gamma Oryzanol on Toll-Like Receptor 4: Receptor Structure-Based Pharmacophore, Hit Identification, and In Silico Evidence up Pharmacognostic Authentication and Phytochemical Profiling Coupled with Flowability Studies of Zingiber officinale for Quality Control ›