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Spinosin, a C-Glucosylflavone, from Zizyphus jujuba var. spinosa Ameliorates Abeta1-42 Oligomer-Induced Memory Impairment in Mice
Biomolecules & Therapeutics ; : 156-164, 2015.
Article in English | WPRIM | ID: wpr-104379
ABSTRACT
Alzheimer's disease (AD) is a neurodegenerative disorder associated with progressive memory loss and neuronal cell death. Although numerous previous studies have been focused on disease progression or reverse pathological symptoms, therapeutic strategies for AD are limited. Alternatively, the identification of traditional herbal medicines or their active compounds has received much attention. The aims of the present study were to characterize the ameliorating effects of spinosin, a C-glucosylflavone isolated from Zizyphus jujuba var. spinosa, on memory impairment or the pathological changes induced through amyloid-beta1-42 oligomer (AbetaO) in mice. Memory impairment was induced by intracerebroventricular injection of AbetaO (50 muM) and spinosin (5, 10, and 20 mg/kg) was administered for 7 days. In the behavioral tasks, the subchronic administration of spinosin (20 mg/kg, p.o.) significantly ameliorated AbetaO-induced cognitive impairment in the passive avoidance task or the Y-maze task. To identify the effects of spinosin on the pathological changes induced through AbetaO, immunohistochemistry and Western blot analyses were performed. Spinosin treatment also reduced the number of activated microglia and astrocytes observed after AbetaO injection. In addition, spinosin rescued the AbetaO-induced decrease in choline acetyltransferase expression levels. These results suggest that spinosin ameliorated memory impairment induced through AbetaO, and these effects were regulated, in part, through neuroprotective activity via the anti-inflammatory effects of spinosin. Therefore, spinosin might be a useful agent against the amyloid b protein-induced cognitive dysfunction observed in AD patients.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Immunohistochemistry / Blotting, Western / Astrocytes / Choline O-Acetyltransferase / Cell Death / Microglia / Disease Progression / Neurodegenerative Diseases / Ziziphus / Alzheimer Disease Limits: Animals / Humans Language: English Journal: Biomolecules & Therapeutics Year: 2015 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Immunohistochemistry / Blotting, Western / Astrocytes / Choline O-Acetyltransferase / Cell Death / Microglia / Disease Progression / Neurodegenerative Diseases / Ziziphus / Alzheimer Disease Limits: Animals / Humans Language: English Journal: Biomolecules & Therapeutics Year: 2015 Type: Article