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抗氧化剂α-硫辛酸和N-乙酰半胱氨酸可逆转衰老的SAMP8小鼠的记忆损伤和脑氧化应激。

The antioxidants alpha-lipoic acid and N-acetylcysteine reverse memory impairment and brain oxidative stress in aged SAMP8 mice.

作者信息

Farr Susan A, Poon H Fai, Dogrukol-Ak Dilek, Drake Jeniffer, Banks William A, Eyerman Edward, Butterfield D Allan, Morley John E

机构信息

Geriatric Research Education and Clinical Center (GRECC), VA Medical Center (151/JC), 915 N. Grand Boulevard, St. Louis, MO 63109, USA.

出版信息

J Neurochem. 2003 Mar;84(5):1173-83. doi: 10.1046/j.1471-4159.2003.01580.x.

Abstract

Oxidative stress may play a crucial role in age-related neurodegenerative disorders. Here, we examined the ability of two antioxidants, alpha-lipoic acid (LA) and N-acetylcysteine (NAC), to reverse the cognitive deficits found in the SAMP8 mouse. By 12 months of age, this strain develops elevated levels of Abeta and severe deficits in learning and memory. We found that 12-month-old SAMP8 mice, in comparison with 4-month-old mice, had increased levels of protein carbonyls (an index of protein oxidation), increased TBARS (an index of lipid peroxidation) and a decrease in the weakly immobilized/strongly immobilized (W/S) ratio of the protein-specific spin label MAL-6 (an index of oxidation-induced conformational changes in synaptosomal membrane proteins). Chronic administration of either LA or NAC improved cognition of 12-month-old SAMP8 mice in both the T-maze footshock avoidance paradigm and the lever press appetitive task without inducing non-specific effects on motor activity, motivation to avoid shock, or body weight. These effects probably occurred directly within the brain, as NAC crossed the blood-brain barrier and accumulated in the brain. Furthermore, treatment of 12-month-old SAMP8 mice with LA reversed all three indexes of oxidative stress. These results support the hypothesis that oxidative stress can lead to cognitive dysfunction and provide evidence for a therapeutic role for antioxidants.

摘要

氧化应激可能在与年龄相关的神经退行性疾病中起关键作用。在此,我们研究了两种抗氧化剂,α-硫辛酸(LA)和N-乙酰半胱氨酸(NAC),逆转SAMP8小鼠认知缺陷的能力。到12月龄时,该品系小鼠的β-淀粉样蛋白水平升高,学习和记忆出现严重缺陷。我们发现,与4月龄小鼠相比,12月龄的SAMP8小鼠的蛋白质羰基(蛋白质氧化指标)水平升高、硫代巴比妥酸反应物(脂质过氧化指标)增加,并且蛋白质特异性自旋标记物MAL-6的弱固定/强固定(W/S)比值降低(突触体膜蛋白氧化诱导构象变化的指标)。在T迷宫足部电击回避范式和杠杆按压奖赏任务中,长期给予LA或NAC均可改善12月龄SAMP8小鼠的认知,且对运动活动、避免电击的动机或体重无非特异性影响。这些作用可能直接发生在脑内,因为NAC可穿过血脑屏障并在脑内蓄积。此外,用LA处理12月龄的SAMP8小鼠可逆转氧化应激的所有三个指标。这些结果支持氧化应激可导致认知功能障碍的假说,并为抗氧化剂的治疗作用提供了证据。

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