Center for Neuroscience and Cell Biology of Coimbra, University of Coimbra, Portugal.
Ageing Res Rev. 2011 Apr;10(2):264-73. doi: 10.1016/j.arr.2011.01.001. Epub 2011 Jan 22.
Severe abnormalities in brain glucose/energy metabolism and insulin signaling have been documented to take a pivotal role in early sporadic Alzheimer's disease (sAD) pathology. Indeed, the "insulin-resistant brain state" has been hypothesized to form the core of the neurodegenerative events that occur in sAD. In this vein, intracerebroventricular administration of subdiabetogenic doses of streptozotocin (STZ) in rats can induce an insulin-resistant brain state, which is proposed as a suitable experimental model of sAD. This review highlights the involvement of disturbed brain insulin metabolism in sAD etiopathogenesis. Furthermore, current knowledge demonstrates that central STZ administration produces brain pathology and behavioral changes that resemble changes found in sAD patients. The STZ-intracerebroventricularly treated rat represents a promising experimental tool in this field by providing new insights concerning early brain alterations in sAD, which can be translated in novel etiopathogenic and therapeutic approaches in this disease.
严重的脑葡萄糖/能量代谢和胰岛素信号异常被认为在早期散发性阿尔茨海默病(sAD)病理中起关键作用。事实上,“胰岛素抵抗的大脑状态”被假设为发生在 sAD 中的神经退行性事件的核心。从这个角度来看,向大鼠的侧脑室给予亚糖尿病剂量的链脲佐菌素(STZ)可以诱导出一种胰岛素抵抗的大脑状态,这被提议作为 sAD 的合适实验模型。本综述强调了脑胰岛素代谢紊乱在 sAD 发病机制中的作用。此外,目前的知识表明,中枢 STZ 给药会导致类似于 sAD 患者中发现的大脑病理学和行为变化。通过提供关于 sAD 早期大脑改变的新见解,侧脑室注射 STZ 的大鼠成为该领域有前途的实验工具,可转化为该疾病的新发病机制和治疗方法。