蜂胶对阿尔茨海默氏症模型小鼠认知能力下降的预防作用

IF 3.7 3区 医学 Q2 GERIATRICS & GERONTOLOGY
Ryo Inagaki , Tohru Yamakuni , Takashi Saito , Takaomi C. Saido , Shigeki Moriguchi
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引用次数: 0

摘要

巴西绿蜂胶(蜂胶)是一种化学性质复杂的树脂物质,是治疗阿尔茨海默病的潜在药物。在这里,蜂胶诱导了神经-2A细胞内钙浓度([Ca])的短暂升高;此外,蜂胶诱导的[Ca]升高在用淀粉样β预处理24小时之前被抑制。为了揭示[Ca]升高对认知障碍的影响,我们在APP-KI小鼠4个月大和12个月大时对其进行了与记忆相关的行为任务。在连续8周服用300-1000 mg/kg/d蜂胶的情况下,APP-KI小鼠在4个月大时的认知障碍明显改善,但在12个月大时则没有明显改善。与行为学观察结果一致,APP-KI小鼠在4个月大时反复服用蜂胶后,受损的海马长期潜能明显改善。此外,反复服用蜂胶还能显著激活APP-KI小鼠CA1区的细胞内钙信号通路。这些结果表明,蜂胶通过激活AD小鼠CA1区细胞内钙信号通路,对认知功能衰退有预防作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preventive effect of propolis on cognitive decline in Alzheimer’s disease model mice

Brazilian green propolis (propolis) is a chemically complex resinous substance that is a potentially viable therapeutic agent for Alzheimer’s disease. Herein, propolis induced a transient increase in intracellular Ca2+ concentration ([Ca2+]i) in Neuro-2A cells; moreover, propolis-induced [Ca2+]i elevations were suppressed prior to 24-h pretreatment with amyloid-β. To reveal the effect of [Ca2+]i elevation on impaired cognition, we performed memory-related behavioral tasks in APP-KI mice relative to WT mice at 4 and 12 months of age. Propolis, at 300–1000 mg/kg/d for 8 wk, significantly ameliorated cognitive deficits in APP-KI mice at 4 months, but not at 12 months of age. Consistent with behavioral observations, injured hippocampal long-term potentiation was markedly ameliorated in APP-KI mice at 4 months of age following repeated propolis administration. In addition, repeated administration of propolis significantly activated intracellular calcium signaling pathway in the CA1 region of APP-KI mice. These results suggest a preventive effect of propolis on cognitive decline through the activation of intracellular calcium signaling pathways in CA1 region of AD mice model.

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来源期刊
Neurobiology of Aging
Neurobiology of Aging 医学-老年医学
CiteScore
8.40
自引率
2.40%
发文量
225
审稿时长
67 days
期刊介绍: Neurobiology of Aging publishes the results of studies in behavior, biochemistry, cell biology, endocrinology, molecular biology, morphology, neurology, neuropathology, pharmacology, physiology and protein chemistry in which the primary emphasis involves mechanisms of nervous system changes with age or diseases associated with age. Reviews and primary research articles are included, occasionally accompanied by open peer commentary. Letters to the Editor and brief communications are also acceptable. Brief reports of highly time-sensitive material are usually treated as rapid communications in which case editorial review is completed within six weeks and publication scheduled for the next available issue.
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