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首页> 外文期刊>NeuroMolecular Medicine >Effects of Dietary Supplementation with N-Acetyl Cysteine, Acetyl-l-Carnitine and S-Adenosyl Methionine on Cognitive Performance and Aggression in Normal Mice and Mice Expressing Human ApoE4
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Effects of Dietary Supplementation with N-Acetyl Cysteine, Acetyl-l-Carnitine and S-Adenosyl Methionine on Cognitive Performance and Aggression in Normal Mice and Mice Expressing Human ApoE4

机译:日粮添加N-乙酰半胱氨酸,乙酰-1-肉碱和S-腺苷甲硫氨酸对正常小鼠和表达人ApoE4的小鼠认知能力和攻击能力的影响

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摘要

In addition to cognitive impairment, behavioral changes such as aggressive behavior, depression, and psychosis accompany Alzheimer’s Disease. Such symptoms may arise due to imbalances in neurotransmitters rather than overt neurodegeneration. Herein, we demonstrate that combined administration of N-acetyl cysteine (an antioxidant and glutathione precursor that protects against Abeta neurotoxicity), acetyl-l-carnitine (which raises ATP levels, protects mitochondria, and buffers Abeta neurotoxicity), and S-adenosylmethionine (which facilitates glutathione usage and maintains acetylcholine levels) enhanced or maintain cognitive function, and attenuated or prevented aggression, in mouse models of aging and neurodegeneration. Enhancement of cognitive function was rapidly reversed upon withdrawal of the formulation and restored following additional rounds supplementation. Behavioral abnormalities correlated with a decline in acetylcholine, which was also prevented by this nutriceutical combination, suggesting that neurotransmitter imbalance may contribute to their manifestation. Treatment with this nutriceutical combination was able to compensate for lack of dietary folate and vitamin E, coupled with administration of dietary iron as a pro-oxidant (which collectively increase homocysteine and oxidative damage to brain tissue), indicating that it provided antioxidant neuroprotection. Maintenance of neurotransmitter levels and prevention of oxidative damage underscore the efficacy of a therapeutic approach that utilizes a combination of neuroprotective agents.
机译:除认知障碍外,阿尔茨海默氏病还伴有攻击性行为,抑郁和精神病等行为改变。此类症状可能是由于神经递质失衡而不是明显的神经变性引起的。在本文中,我们证明N-乙酰半胱氨酸(抗Abeta神经毒性的抗氧化剂和谷胱甘肽前体),乙酰基-1-肉碱(提高ATP水平,保护线粒体和缓冲Abeta神经毒性)和S-腺苷甲硫氨酸(在衰老和神经退行性疾病的小鼠模型中,它有助于谷胱甘肽的使用并维持乙酰胆碱水平)增强或维持认知功能,减弱或防止侵略。撤回制剂后,认知功能的增强迅速逆转,并在补充回合后恢复。行为异常与乙酰胆碱的下降有关,这也可以通过这种营养组合来预防,这表明神经递质失衡可能是其表现的原因。这种营养组合的治疗能够弥补饮食中叶酸和维生素E的缺乏,再加上饮食中铁作为前氧化剂(共同增加同型半胱氨酸和对脑组织的氧化损伤),表明它提供了抗氧化神经保护作用。维持神经递质水平和防止氧化损伤强调了利用神经保护剂组合的治疗方法的有效性。

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