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Updated: Jul 16, 2026

Preparation of Acute Hippocampal Slices from Rats and Transgenic Mice for the Study of Synaptic Alterations during Aging and Amyloid Pathology
Published on: March 23, 2011
Ficus deltoidea Preserves Hippocampal Neuronal Integrity and Redox Balance in Oxidative Stress-Driven Alzheimer's
Alhaji Modu Bukar1,2, Che Mohd Nasril Che Mohd Nassir3, Michael Ayuba1,2
1Department of Human Anatomy, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400 UPM, Serdang, Selangor, Malaysia.
Abstract:
Alzheimer's disease (AD) is a progressive neurodegenerative disorder and the leading cause of dementia worldwide, with oxidative stress playing a central role in its pathogenesis. Ficus deltoidea (FD), a medicinal plant rich in flavonoids vitexin and isovitexin, possesses potent antioxidant and anti-inflammatory properties, yet its neuroprotective efficacy in AD remains incompletely characterized. This study investigated the protective effects of FD in a D-galactose- and aluminum chloride (AlCl3)-induced oxidative stress-driven AD-like rat model using behavioral, histological, ultrastructural, and biochemical approaches. Fifty-four male Wistar rats were assigned to six groups: control, AD-like model, donepezil (1 mg/kg), and FD-treated groups (50, 100, and 200 mg/kg) for 10 weeks. Anxiety-like behavior and spatial working memory were assessed using the elevated plus maze (EPM) and T-maze tests, respectively. Hippocampal neuronal integrity was evaluated by hematoxylin and eosin (H&E) staining and transmission electron microscopy (TEM), while oxidative stress biomarkers (MDA, CAT, T-SOD, CuZn-SOD, and HO-1) were quantified using ELISA. FD treatment, particularly at 200 mg/kg, significantly improved spatial working memory and normalized anxiety-related behavior, with treatment responses approaching those observed in the donepezil-treated group. Histological analyses revealed preservation of pyramidal neurons across CA1, CA2, CA3, and dentate gyrus subregions, while ultrastructural studies demonstrated marked protection of mitochondrial integrity, myelin sheath organization, and smooth endoplasmic reticulum morphology. Biochemically, FD significantly reduced lipid peroxidation and enhanced endogenous antioxidant defenses. In conclusion, FD exerted significant neuroprotective effects characterized by preservation of hippocampal structure, maintenance of neuronal ultrastructure, and restoration of redox homeostasis in an oxidative stress-driven AD-like model. These findings demonstrate that FD mitigates oxidative stress-associated neuronal injury and cognitive impairment in a D-galactose and AlCl3-induced AD-like rat model, supporting its potential as a phytotherapeutic candidate for oxidative stress-related neurodegeneration. However, further studies are required to determine its effects on canonical Alzheimer's disease pathologies, including amyloid and tau abnormalities.
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