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首页> 外文期刊>Innovation in aging. >Reversing Cognitive Decline in Aging: Reversible Mechanistic Defects and a Novel Nutritional Intervention
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Reversing Cognitive Decline in Aging: Reversible Mechanistic Defects and a Novel Nutritional Intervention

机译:逆转老龄化的认知下降:可逆机制缺陷和新的营养干预

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Abstract Aging is the biggest risk factor for cognitive-decline and Alzheimer’s disease (AD), but underlying mechanisms are not well-understood and interventions are lacking. Cognitive-decline in AD has been associated with deficiency of glutathione, (the most abundant, intracellular, antioxidant protein), elevated oxidative-stress, insulin-resistance and increased inflammation. We identified and reported that glutathione-deficiency and oxidative-stress in older-adults occur due to decreased availability of precursor amino-acids glycine and cysteine, and can be corrected with GlyNAC (a combination of glycine and the cysteine precursor N-acetylcysteine). We hypothesized that cognitive decline in older-adults is linked to glutathione-deficiency, mitochondrial-dysfunction, oxidative-stress, insulin-resistance, and inflammation. The first abstract discusses the rationale and findings of an open-label clinical trial: compared to young-humans, older-adults had cognitive-decline, glutathione-deficiency, mitochondrial-dysfunction, abnormal glucose-metabolism and insulin-resistance, oxidative-stress, endothelial-dysfunction and inflammation. These defects were improved/reversed by supplementing GlyNAC for 24-weeks, but benefits receded on stopping GlyNAC for 12-weeks. The second abstract presents a study in 8 young (20-weeks old) and 16 aged (90-weeks old) wild-type male C57BL/6J mice where we found that aged-mice had naturally-occurring cognitive-impairment, and brain defects in glutathione-deficiency, oxidative-stress, glucose-transport, mitochondrial glucose-oxidation, insulin-resistance, endoplasmic-reticulum stress, autophagy, mitophagy, inflammation, senescence, genomic and telomere damage. Aged-mice received either GlyNAC or isonitrogenous-placebo supplementation for 8-weeks, and only GlyNAC-fed mice improved cognition and brain defects. Collectively these data highlights the discovery of novel and reversible mechanistic defects in older-adults and aged-mice with naturally-occurring cognitive-decline, and identifies that supplementing GlyNAC can improve brain-health and cognition. These findings could have important implications for reversing cognitive-decline in older-adults, and AD.
机译:摘要衰老是认知衰退和阿尔茨海默病(AD)的最大危险因素,但潜在的机制不是很好地理解,并且缺乏干预措施。 AD的认知 - 下降已经与谷胱甘肽的缺乏有关,(最丰富,细胞内,抗氧化蛋白),氧化 - 应激升高,胰岛素抗性和炎症增加。我们鉴定并据报道,由于前体氨基酸甘氨酸和半胱氨酸的可用性降低,较老年人的谷胱甘肽缺乏和氧化 - 应激发生,并且可以用Glynac(甘氨酸和半胱氨酸前体N-乙酰半胱氨酸的组合)校正。我们假设老年人的认知下降与谷胱甘肽缺乏,线粒体功能障碍,氧化 - 应激,胰岛素抗性和炎症相关联。第一个摘要讨论了开放标签临床试验的理由和结果:与年轻人相比,老年人具有认知 - 下降,谷胱甘肽缺乏,线粒体功能障碍,葡萄糖 - 代谢异常和胰岛素抗性,氧化 - 应激,内皮功能障碍和炎症。通过补充Glynac 24周的含量改善/逆转这些缺陷,但在止动甘露那克持续12周后取出的益处。第二篇抽象呈现在8名年轻(20周龄)和16岁(90周龄)的野生型男性C57BL / 6J老鼠中的一项研究,在那里,我们发现老鼠患者具有自然发生的认知障碍和脑缺陷在谷胱甘肽缺乏,氧化 - 应激,葡萄糖 - 转运,线粒体葡萄糖 - 氧化,胰岛素抵抗,内质 - 网状应力,自噬,水肿,炎症,衰老,基因组和端粒损伤。老年小鼠接受了8周的甘露那克或异孕 - 安慰剂补充剂,并且只有Glynac-Fed小鼠改善了认知和脑缺陷。总的来说这些数据突出了在较老年人和具有自然发生的认知衰退的老年人和昔阳小鼠中发现了新的和可逆机制缺陷,并确定了补充甘露那克可以改善脑健康和认知。这些调查结果可能对逆转老年人的认知衰退和广告来说具有重要意义。

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