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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Decreased transketolase activity contributes to impaired hippocampal neurogenesis induced by thiamine deficiency.
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Decreased transketolase activity contributes to impaired hippocampal neurogenesis induced by thiamine deficiency.

机译:转酮醇酶活性降低导致硫胺素缺乏引起的海马神经发生受损。

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Thiamine deficiency (TD) impairs hippocampal neurogenesis. However, the mechanisms involved are not identified. In this work, TD mouse model was generated using a thiamine-depleted diet at two time points, TD9 and TD14 for 9 and 14 days of TD respectively. The activities of pyruvate dehydrogenase (PDH), alpha-ketoglutamate dehydrogenase (KGDH), glucose-6-phosphate dehydrogenase (G6PD), and transketolase (TK), as well as on the contents of NADP(+) and NADPH were determined in whole mouse brain, isolated cortex, and hippocampus of TD mice model. The effects of TK silencing on the growth and migratory ability of cultured hippocampal progenitor cells (HPC), as well as on neuritogenesis of hippocampal neurons were explored. The results showed that TD specifically reduced TK activity in both cortex and hippocampus, without significantly affecting the activities of PDH, KGDH, and G6PD in TD9 and TD14 groups. The level of whole brain and hippocampal NADPH in TD14 group were significantly lower than that of control group. TK silencing significantly inhibited the proliferation, growth, and migratory abilities of cultured HPC, without affecting neuritogenesis of cultured hippocampal neurons. Taken together, these results demonstrate that decreased TK activity leads to pentose-phosphate pathway dysfunction and contributes to impaired hippocampal neurogenesis induced by TD. TK and pentose-phosphate pathway may be considered new targets to investigate hippocampal neurogenesis.
机译:硫胺素缺乏症(TD)损害海马神经发生。但是,尚未确定所涉及的机制。在这项工作中,使用贫硫胺素饮食在TD9和TD14两个时间点分别对TD的9天和14天生成了TD小鼠模型。完整测定了丙酮酸脱氢酶(PDH),α-酮戊二酸脱氢酶(KGDH),葡萄糖-6-磷酸脱氢酶(G6PD)和转酮醇酶(TK)的活性以及NADP(+)和NADPH的含量TD小鼠模型的小鼠大脑,分离的皮质和海马体。探索了TK沉默对培养的海马祖细胞(HPC)的生长和迁移能力以及海马神经元神经发生的影响。结果表明,TD特异性降低了皮质和海马的TK活性,而没有显着影响TD9和TD14组的PDH,KGDH和G6PD活性。 TD14组全脑和海马NADPH水平明显低于对照组。 TK沉默可显着抑制培养的HPC的增殖,生长和迁移能力,而不会影响培养的海马神经元的神经形成。综上所述,这些结果表明TK活性降低导致戊糖-磷酸途径功能障碍,并导致由TD诱导的海马神经发生受损。 TK和戊糖磷酸途径可能被认为是研究海马神经发生的新靶标。

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