Memantine versus Ginkgo biloba Extract: A Comparative Study on Cognitive Dysfunction Treatment in a Novel Rat Model.

Autor:	Allam EAH; Department of Pharmacology and Toxicology, Faculty of Pharmacy, Assiut University, Assiut, Egypt., Assi AA; Department of Pharmacology, Faculty of Medicine, Assiut University, Assiut, Egypt., Badary DM; Department of Pathology, Faculty of Medicine, Assiut University, Assiut, Egypt., Farrag MMY; Department of Pharmacology, Faculty of Medicine, Assiut University, Assiut, Egypt., Nicola MA; Department of Pharmacology and Toxicology, Faculty of Pharmacy, Assiut University, Assiut, Egypt.
Jazyk:	angličtina
Zdroj:	Planta medica [Planta Med] 2024 Apr; Vol. 90 (4), pp. 286-297. Date of Electronic Publication: 2024 Jan 29.
DOI:	10.1055/a-2245-3624
Abstrakt:	Extracellular senile plaques and intraneuronal neurofibrillary tangles are two devastating brain proteinopathies that are indicative of Alzheimer's disease, the most prevalent type of dementia. Currently, no effective medications are available to stop or reverse Alzheimer's disease. Ginkgo biloba extract, commonly referred to as EGb 761, is a natural product made from the leaves of the G. biloba tree. It has long been demonstrated to have therapeutic benefits in Alzheimer's disease. The current study assessed the beneficial effects of EGb 761 against Alzheimer's disease in comparison with memantine, a standard treatment for Alzheimer's disease. The scopolamine-heavy metals mixture rat Alzheimer's disease model is a newly created model to study the effects of EGb 761 oral therapy on cognitive performance and other Alzheimer's disease-like changes over a 28-day experimental period. This new Alzheimer's disease model provides better criteria for Alzheimer's disease hallmarks than the conventional scopolamine model. The EGb 761 reversed memory and learning deficits induced by the scopolamine-heavy metals mixture. These outcomes were linked to a more pronounced inhibitory effect on acetylcholinesterase, caspase-3, hippocampal amyloid-beta protein (A β 1 - 42), phosphorylated tau protein counts, and proinflammatory cytokines (tumor necrosis factor- α and interleukin-1 β ) compared to the memantine-treated group. Furthermore, EGb 761 treatment considerably reduced lipid peroxidation (malondialdehyde) and improved reduced glutathione levels compared to memantine. Our results suggest EGb 761's potential in treating central nervous system disorders. It's a promising candidate for future Alzheimer's disease therapeutic exploration. This study also highlights the need for future research to focus on the positive benefits of herbal medicines. Competing Interests: The authors declare that they have no conflict of interest. (Thieme. All rights reserved.)
Databáze:	MEDLINE
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