首页> 外文期刊>Bioscience, Biotechnology, and Biochemistry >Vitamin B1-deficient mice show impairment of hippocampus-dependent memory formation and loss of hippocampal neurons and dendritic spines: potential microendophenotypes of Wernicke-Korsakoff syndrome
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Vitamin B1-deficient mice show impairment of hippocampus-dependent memory formation and loss of hippocampal neurons and dendritic spines: potential microendophenotypes of Wernicke-Korsakoff syndrome

机译:维生素B1缺陷小鼠表现出海马依赖性记忆形成和海马神经元和树突脊柱损失的损害:Wernicke-Korsakoff综合征的潜在微生物术

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摘要

Patients with severe Wernicke-Korsakoff syndrome (WKS) associated with vitamin B1 (thiamine) deficiency (TD) show enduring impairment of memory formation. The mechanisms of memory impairment induced by TD remain unknown. Here, we show that hippocampal degeneration is a potential microendophenotype (an endophenotype of brain disease at the cellular and synaptic levels) of WKS in pyrithiamine-induced thiamine deficiency (PTD) mice, a rodent model of WKS. PTD mice show deficits in the hippocampus-dependent memory formation, although they show normal hippocampus-independent memory. Similarly with WKS, impairments in memory formation did not recover even at 6months after treatment with PTD. Importantly, PTD mice exhibit a decrease in neurons in the CA1, CA3, and dentate gyrus (DG) regions of the hippocampus and reduced density of wide dendritic spines in the DG. Our findings suggest that TD induces hippocampal degeneration, including the loss of neurons and spines, thereby leading to enduring impairment of hippocampus-dependent memory formation.
机译:与维生素B1(硫胺素)缺陷相关的严重Wernicke-Korsakoff综合征(WKS)的患者表现出持久的记忆形成损害。 TD引起的内存损伤机制仍然是未知的。在这里,我们表明海马变性是裂解硫胺素诱导的硫胺素缺乏(PTD)小鼠的WKS潜在的微生物型(在细胞和突触水平的脑疾病的内心型),WKS的啮齿动物模型。 PTD小鼠在依赖性存储器形成中显示了缺陷的缺陷,尽管它们显示了普通的海马独立存储器。与WKS同样,在用PTD处理后,甚至在6个月内的记忆形成损伤也没有恢复。重要的是,PTD小鼠在海马的Ca1,Ca 3和牙齿的齿状物(dg)区域中的神经元减少,并且Dg中的宽树突刺的密度降低。我们的研究结果表明,TD诱导海马退化,包括神经元和刺的损失,从而导致海马依赖性记忆形成的持久损害。

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