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衰老加速 SAMP8 小鼠和阿尔茨海默病患者海马中 RNA 的氧化损伤和 MTH1 的表达模式。

Oxidative damage to RNA and expression patterns of MTH1 in the hippocampi of senescence-accelerated SAMP8 mice and Alzheimer's disease patients.

机构信息

The Key Laboratory of Geriatrics, Beijing Hospital, Beijing Institute of Geriatrics, Ministry of Health, No. 1, DaHua Road, Dong Dan, 100730, Beijing, People's Republic of China.

出版信息

Neurochem Res. 2011 Aug;36(8):1558-65. doi: 10.1007/s11064-011-0484-4. Epub 2011 May 3.

Abstract

Mammalian MTH1 protein, a MutT-related protein, catalyzes the hydrolysis of 8-oxo-7,8-dihydroguanosine triphosphate (8-oxoGTP) to monophosphate, thereby preventing incorporation of 8-oxo-7,8-dihydroguanine (8-oxoguanine) into RNA. In this study, we applied immunohistochemistry to follow the expression of MTH1 and the amount of 8-oxoguanine in RNA during aging. There were increased amounts of 8-oxoguanine in RNA in the CAl and CA3 subregions of hippocampi of 8- and 12-month-old SAMP8 mice, which exhibited early aging syndromes and declining learning and memory abilities compared to those of age-matched control SAMR1 mice. The expression levels of MTH1 in the hippocampi of 8- and 12-month-old SAMP8 mice were significantly lower than those of control mice. Therefore, in this mouse model, age-related accumulation of 8-oxoguanine in RNA is correlated with decreased expression of MTH1. Increased amounts of 8-oxoguanine in the RNA, and decreased expression of MTH1 were also observed in the hippocampi of patients suffering from Alzheimer's disease. These results suggest that MTH1 deficiency might be a causative factor for aging and age-related disorders.

摘要

哺乳动物 MTH1 蛋白是一种 MutT 相关蛋白,可催化 8-氧代-7,8-二氢鸟苷三磷酸(8-氧代 GTP)水解为单磷酸,从而防止 8-氧代-7,8-二氢鸟嘌呤(8-氧鸟嘌呤)掺入 RNA 中。在这项研究中,我们应用免疫组织化学技术来研究 MTH1 的表达和 RNA 中 8-氧鸟嘌呤的含量随衰老的变化。与年龄匹配的对照 SAMR1 小鼠相比,表现出早期衰老综合征和学习记忆能力下降的 8 个月和 12 个月大的 SAMP8 小鼠海马 CA1 和 CA3 亚区的 RNA 中 8-氧鸟嘌呤的含量增加。8 个月和 12 个月大的 SAMP8 小鼠海马中的 MTH1 表达水平明显低于对照小鼠。因此,在这种小鼠模型中,与年龄相关的 RNA 中 8-氧鸟嘌呤的积累与 MTH1 表达的降低有关。在患有阿尔茨海默病的患者的海马中也观察到 RNA 中 8-氧鸟嘌呤的含量增加和 MTH1 的表达降低。这些结果表明,MTH1 缺乏可能是衰老和与年龄相关疾病的一个致病因素。

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