Analysis of CA1, CA3, and DG areas of the hippocampus, substance-P, and brain-derived neurotrophic factors expression in the presence of Ocimum sanctum Linn on the brain of the rat model Alzheimer’s disease

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Made Bagus Auriva Mataram, Ulayatul Kustiati, Hevi Wihadmadyatami, Dwi Aris Agung Nugrahaningsih, Siti Isrina Oktavia Salasia, Dwi Liliek Kusindarta

2025 Open Veterinary Journal Vol. 15 Issue 2 Article Cited by 0 Quartile

Abstract

Background: Alzheimer’s disease (AD) is a progressive neurological condition characterized by impaired cognitive dysfunction and abnormal behavior. Thirty-five million individuals worldwide suffer from dementia, making it the most frequent cause of dementia. Canine cognitive dysfunction (CCD) affects 28% of dogs aged 11–12 years. It is a prevalent disease in canines. Amyloid-β peptides accumulate neurotoxicity, resulting in problems in the central nervous system and neurotransmitters. Treatments for both AD and CCD have not yet shown acceptable outcomes. It is crucial to comprehend disease mechanisms and identify novel therapeutics using animal models. Aim: Using a rat model of AD, this study attempted to determine the effects of an ethanolic extract from Ocimum sanctum on the number and shape of neurons in the CA1, CA3, and DG sections of the hippocampus along with the expression of neurotrophic factors. Methods: The animal model will be split into five treatment groups, one of which will be a control group. The treatments will be administered for 14, 21, and 28 days, and samples will be analyzed by BDNF by ELISA, SP expression by immunohistochemical staining, and the number of neurons in CA1, CA3, and DG using cresyl violet staining. Results: Results of the study revealed increased neuronal density in the CA1, CA3, and DG regions, and these neurons were more highly expressed in the neurotrophic factor BDNF and neuropeptide SP. Conclusion: By upregulating the expression of SP and BDNF, the ethanolic extract of O. sanctum increased the neuronal counts (pyramidal and granular cells) in the hippocampal CA1, CA3, and DG regions. © 2025, Faculty of Veterinary Medicine, University of Tripoli. All rights reserved.

Affiliations

Post-graduate School of Faculty of Veterinary Medicine, Universitas Gadjah Mada, Yogyakarta, Indonesia; Laboratory of Clinical Pathology, Faculty of Veterinary Medicine, Brawijaya University, Malang, Indonesia; Laboratory of Pharmacology, Faculty of Veterinary Medicine, Universitas Brawijaya, Malang, Indonesia; Department of Anatomy, Faculty of Veterinary Medicine, Universitas Gadjah Mada, Yogyakarta, Indonesia; Department of Pharmacology and Therapy, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia; Department of Clinical Pathology, Faculty of Veterinary Medicine, Universitas Gadjah Mada, Yogyakarta, Indonesia