Suppr超能文献

雄性2型糖尿病Goto-Kakizaki大鼠皮质神经元丢失的证据。

Evidence for cortical neuronal loss in male type 2 diabetic Goto-Kakizaki rats.

作者信息

Hussain Shafaat, Mansouri Shiva, Sjöholm Åke, Patrone Cesare, Darsalia Vladimer

机构信息

Department of Clinical Science and Education, Internal Medicine, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.

Department of Biochemistry and Molecular Biology, College of Medicine, University of South Alabama, Mobile, AL, USA Department of Internal Medicine, Diabetes Research Unit, Södertälje Hospital, Södertälje, Sweden.

出版信息

J Alzheimers Dis. 2014;41(2):551-60. doi: 10.3233/JAD-131958.

Abstract

Type 2 diabetes (T2D) is strongly associated with early cognitive decline and may facilitate the development of neurodegenerative diseases. Despite the overwhelming amount of indirect evidence pointing toward the presence of cerebral neurodegeneration in T2D, no hard proof of it on histological and quantitative levels exists. This warrants more research to investigate whether T2D can lead to neurodegeneration in the central nervous system and to study the precise nature and temporal dynamics of such changes. We performed a comprehensive quantitative assessment of T2D-induced changes in neuronal and glial numbers in the cerebral cortex using stereological methods. We compared the cellular composition of 3- and 13-month-old male type 2 diabetic Goto-Kakizaki (GK) rat brains. Age and sex-matched Wistar rats served as healthy controls. Our results show a significant decrease in neuron numbers (≈11%) in the cerebral cortex of 13-month-old GK rats compared to young, or Wistar rats, while astroglia numbers were unchanged. We also recorded increased microglia activation in aged diabetic rat brains as indicated by significantly increased average microglia cell volume. Our observations provide quantitative evidence of T2D-induced changes in brain's cellular composition during aging. These findings may facilitate the mechanistic understanding of cognitive dysfunction and other neurodegenerative disorders in T2D.

摘要

2型糖尿病(T2D)与早期认知衰退密切相关,可能会促进神经退行性疾病的发展。尽管有大量间接证据表明T2D存在脑内神经变性,但在组织学和定量水平上尚无确凿证据。这就需要更多研究来调查T2D是否会导致中枢神经系统神经变性,并研究这种变化的确切性质和时间动态。我们使用体视学方法对T2D诱导的大脑皮质神经元和神经胶质细胞数量变化进行了全面的定量评估。我们比较了3月龄和13月龄雄性2型糖尿病Goto-Kakizaki(GK)大鼠大脑的细胞组成。年龄和性别匹配的Wistar大鼠作为健康对照。我们的结果显示,与年轻或Wistar大鼠相比,13月龄GK大鼠大脑皮质中的神经元数量显著减少(约11%),而星形胶质细胞数量没有变化。我们还记录到老年糖尿病大鼠大脑中的小胶质细胞激活增加,表现为小胶质细胞平均细胞体积显著增加。我们的观察结果提供了T2D在衰老过程中诱导大脑细胞组成变化的定量证据。这些发现可能有助于从机制上理解T2D中的认知功能障碍和其他神经退行性疾病。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验