首页> 外文期刊>Frontiers in Aging Neuroscience >Iso-α-acids, Hop-Derived Bitter Components of Beer, Attenuate Age-Related Inflammation and Cognitive Decline
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Iso-α-acids, Hop-Derived Bitter Components of Beer, Attenuate Age-Related Inflammation and Cognitive Decline

机译:异α-酸,啤酒的啤酒花苦味成分,减轻与年龄有关的炎症和认知功能下降

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With the aging population rapidly increasing worldwide, preventive measures and treatments for age-related cognitive decline and dementia are of utmost importance. We have previously demonstrated that the consumption of iso-α-acids (IAA), which are hop-derived bitter compounds in beer, prevents the formation of disease pathology in a transgenic mouse model of Alzheimer’s disease (AD). However, the effect of IAA consumption on age-related cognitive decline is unknown. In the present study, we examined the effect of long-term and short-term dietary consumption of IAA, on age-related memory impairments and inflammation in the hippocampus of aged mice. When compared with young mice, aged mice showed impairment in spatial working memory during the Y-maze spontaneous alternation test, impairment in object recognition memory during the novel object recognition test (NORT), a pro-inflammatory hippocampal microglial phenotype with increased CD86 expression and inflammatory cytokine production, increased levels of glutamate and amyloid β _(1–42), and decreased levels of dopamine (DA). In aged mice fed IAA for 3 months, the age-related alterations in memory, microglial inflammation, and glutamate, amyloid β _(1–42), and DA levels were all significantly attenuated. Additionally, the oral administration of IAA for 7 days in aged mice with memory impairment, also improved spatial and object recognition memory. These results suggest that IAA consumption prevents inflammation in the hippocampus and ameliorates age-related cognitive decline.
机译:随着世界范围内老龄化人口的迅速增加,针对与年龄有关的认知能力下降和痴呆症的预防措施和治疗至关重要。先前我们已经证明,啤酒中啤酒花来源的苦味化合物异α-酸(IAA)的食用可防止阿尔茨海默氏病(AD)的转基因小鼠模型中疾病病理的形成。但是,食用IAA对与年龄有关的认知能力下降的影响尚不清楚。在本研究中,我们检查了长期和短期饮食中IAA的摄入对衰老小鼠海马相关的记忆障碍和炎症的影响。与年轻小鼠相比,老年小鼠在Y迷宫自发交替测试中显示空间工作记忆受损,在新型对象识别测试(NORT),CD86表达增加的促炎性海马小神经胶质表型显示对象识别记忆受损。炎症细胞因子的产生,谷氨酸和淀粉样蛋白β_(1-42)的水平升高以及多巴胺(DA)的水平降低。在喂食IAA 3个月的老年小鼠中,与年龄相关的记忆力,小胶质细胞炎症和谷氨酸,淀粉样蛋白β_(1-42)和DA水平均显着减弱。此外,在患有记忆障碍的老年小鼠中口服IAA 7天,也改善了空间和物体识别记忆。这些结果表明食用IAA可以预防海马发炎,并改善与年龄有关的认知能力下降。

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