4.4 Article

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

Journal

BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
Volume 80, Issue 12, Pages 2425-2436

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/09168451.2016.1224639

Keywords

vitamin B1; thiamine deficiency; Wernicke-Korsakoff syndrome; hippocampus-dependent memory; microendophenotypes

Funding

  1. Science Research Promotion Fund
  2. Promotion and Mutual Aid Corporation for Private Schools of Japan [15H02488, 23300120, 20380078]
  3. Challenging Exploratory Research [24650172, 26640014]
  4. Priority Areas-Molecular Brain Science [18022038, 22022039]
  5. Innovative Areas (Research in a proposed research area) [24116008, 24116001, 23115716]
  6. Core Research for Evolutional Science and Technology (CREST), Japan
  7. Sumitomo Foundation, Japan
  8. Naito Foundation, Japan
  9. Takeda Science Foundation, Japan
  10. Grants-in-Aid for Scientific Research [26640014, 15H02488, 24650172, 24116001, 23300120, 24116008] Funding Source: KAKEN

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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.

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