Alpha lipoic acid ameliorates scopolamine induced memory deficit and neurodegeneration in the cerebello-hippocampal cortex
Autor: | Memudu Ae, Abosede Esther Adewumi |
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Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
H&E stain Pharmacology Biochemistry 03 medical and health sciences Cellular and Molecular Neuroscience symbols.namesake 0302 clinical medicine Cortex (anatomy) Medicine Neuroinflammation Glial fibrillary acidic protein biology business.industry Neurodegeneration medicine.disease 030104 developmental biology medicine.anatomical_structure Chromatolysis biology.protein Nissl body symbols Neurology (clinical) Neuron business 030217 neurology & neurosurgery |
Zdroj: | Metabolic Brain Disease. 36:1729-1745 |
ISSN: | 1573-7365 0885-7490 |
Popis: | Scopolamine- induced memory loss is used to study new drug discovery in Alzheimer’s disease (AD) pathogenesis. This study was aimed at evaluating the role of an antioxidant supplement alpha-lipoic acid (AHA), in ameliorating the oxidative damaging effects of scopolamine on cognition, memory, and the neurohistology of the cerebello-hippocampal cortex. Twenty adult male Wistar rats used were categorized into four (4) groups (n = 5): Group A- Control, Group B- 200 mg/kg of AHA, Group C- Scopolamine (memory-impaired model), and Group D- Neurodegenerative repair model (Scopolamine + AHA). The treatment lasted for fourteen (14) days. Y-maze and hang-wire (limb use test) were used as behavioural index to assess memory and motor function while brain tissues were processed for histology (H and E stain), histochemistry using Cresyl Fast violet stain for Nissl bodies, and immunohistochemistry of astrocytes using glial fibrillary acidic protein (GFAP). Results showed that scopolamine led to a decline in brain weight, impaired memory and motor function, induced oxidative tissue damage cumulating in loss of neuronal cells, chromatolysis, the proliferation of reactive astrocytes (neuroinflammation biomarker) in the cerebello-hippocampal cortex; but upon administration of AHA these neuropathological characterizations were inhibited and reversed by AHA demonstrating its antioxidant and neuro- repair potential. In conclusion, AHA is a useful therapeutic agent against scopolamine-induced cognitive and memory deficit because it has the ability to ameliorate oxidative tissue damage by attenuating reactive astrocytes proliferation and neuron chromatolysis thereby improving memory and motor function. |
Databáze: | OpenAIRE |
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