期刊文献+

Locomotor activity and anxiety status, but not spatial working memory,are affected in mice after brief exposure to cuprizone 被引量:4

Locomotor activity and anxiety status, but not spatial working memory,are affected in mice after brief exposure to cuprizone
原文传递
导出
摘要 Chronic long-term exposure to cuprizone causes severe brain demyelination in mice,which leads to changes in locomotion,working memory and anxiety.These findings suggest the importance of intact myelin for these behaviors.This study aimed to investigate the possible behavioral changes in mice with mild oligodendrocyte/myelin damage that parallels the white matter changes seen in the brains of patients with psychiatric disporders.We used the cuprizonetreated mouse model to test both tissue changes and behavioral functions(locomotor activity,anxiety status,and spatial working memory).The results showed that mice given cuprizone in their diet for 7 days had no significant myelin breakdown as evaluated by immunohistochemical staining for myelin basic protein,while the number of mature oligodendrocytes was reduced.The number and length of Caspr protein clusters,a structural marker of the node of Ranvier,did not change.The locomotor activity of the cuprizonetreated mice increased whereas their anxiety levels were lower than in normal controls;spatial working memory,however,did not change.These results,for the first time,link emotion-related behavior with mild white matter damage in cuprizone-treated mice. Chronic long-term exposure to cuprizone causes severe brain demyelination in mice,which leads to changes in locomotion,working memory and anxiety.These findings suggest the importance of intact myelin for these behaviors.This study aimed to investigate the possible behavioral changes in mice with mild oligodendrocyte/myelin damage that parallels the white matter changes seen in the brains of patients with psychiatric disporders.We used the cuprizonetreated mouse model to test both tissue changes and behavioral functions(locomotor activity,anxiety status,and spatial working memory).The results showed that mice given cuprizone in their diet for 7 days had no significant myelin breakdown as evaluated by immunohistochemical staining for myelin basic protein,while the number of mature oligodendrocytes was reduced.The number and length of Caspr protein clusters,a structural marker of the node of Ranvier,did not change.The locomotor activity of the cuprizonetreated mice increased whereas their anxiety levels were lower than in normal controls;spatial working memory,however,did not change.These results,for the first time,link emotion-related behavior with mild white matter damage in cuprizone-treated mice.
出处 《Neuroscience Bulletin》 SCIE CAS CSCD 2013年第5期633-641,共9页 神经科学通报(英文版)
基金 supported by the Manitoba Health Research Council Foundation the Canadian Institutes of Health Research Foundation the Health Science Centre Foundation
关键词 myelination oligodendrocyte locomotor activity anxiety spatial working memory cuprizone mouse myelination oligodendrocyte locomotor activity anxiety spatial working memory cuprizone mouse
  • 相关文献

参考文献28

  • 1Takahashi N, Sakurai T, Davis KL, Buxbaum JD. Linking oligodendrocyte and myelin dysfunction to neurocircuitry abnormalities in schizophrenia. Prog Neurobiol 2011, 93: 13-24.
  • 2Mahon K, Burdick KE, Szeszko PR. A role for white matter abnormalities in the pathophysiology of bipolar disorder. Neurosci Biobehav Rev 2010, 34: 533-554.
  • 3Tham MW, Woon PS, Sum MY, Lee TS, Sire K. White matter abnormalities in major depression: evidence from post- mortem, neuroimaging and genetic studies. J Affect Disord 2011, 132: 26-36.
  • 4Thomason ME, Thompson PM. Diffusion imaging, white matter, and psychopathology. Annu Rev Clin Psycho12011, 7: 63-85.
  • 5D'Agati E, Casarelli L, Pitzianti MB, Pasini A. Overflow movements and white matter abnormalities in ADHD. Prog Neuropsychopharmacol Biol Psychiatry 2010, 34: 441-445.
  • 6Xu H, Li XM. White matter abnormalities and animal models examining a putative role of altered white matter in schizophrenia. Schizophr Res Treatment 2011, 2011: 826976.
  • 7Hiremath MM, Saito Y, Knapp GW, Ting JP, Suzuki K, Matsushima GK. Microglial/macrophage accumulation during cuprizone-induced demyelination in C57BL/6 mice. J Neuroimmuno11998, 92: 38-49.
  • 8Morell P, Barrett CV, Mason JL, Toews AD, Hostettler JD, Knapp GW, et al. Gene expression in brain during cuprizone- induced demyelination and remyelination. Mol Cell Neurosci 1998, 12: 220-227.
  • 9Franco-Pons N, Torrente M, Colomina MT, Vilella E. Behavioral deficits in the cuprizone-induced murine model of demyelination/remyelination. Toxicol Lett 2007, 169: 205- 213.
  • 10Xu H, Yang H J, Zhang Y, Clough R, Browning R, Li XM. Behavioral and neurobiological changes in C57BL/6 miceexposed to cuprizone. Behav Neurosci 2009, 123: 418-429.

同被引文献25

引证文献4

二级引证文献24

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部