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脑内注射链脲佐菌素诱导的散发性阿尔茨海默病猴模型中胰岛素/IGF 信号相关基因的表达。

Insulin/IGF signaling-related gene expression in the brain of a sporadic Alzheimer's disease monkey model induced by intracerebroventricular injection of streptozotocin.

机构信息

National Primate Research Center (NPRC), Korea Research Institute of Bioscience and Biotechnology (KRIBB), Ochang, Korea.

出版信息

J Alzheimers Dis. 2014;38(2):251-67. doi: 10.3233/JAD-130776.

DOI:10.3233/JAD-130776
PMID:23948941
Abstract

We reported previously that the intracerebroventricular streptozotocin (icv-STZ)-treated cynomolgus monkey showed regionally specific glucose hypometabolism in FDG-PET imaging, similar to that observed in the early stages of sporadic Alzheimer's disease (sAD). However, further pathological analyses of this model at the molecular level are needed to validate it as a feasible model for sAD. Two cynomolgus monkeys were injected with 2 mg/kg STZ into the cerebellomedullary cistern at day 1, 7 and 14. Two control monkeys were given normal saline. At 5 months after injection, the expression levels of genes encoding 9 upstream molecules in insulin/insulin-like growth factor (IGF) signaling and markers for 4 cell-type populations in the frontal cortex, hippocampus, posterior cingulate, precuneus, and occipital cortex of control and icv-STZ treated cynomolgus monkeys were examined. Real-time quantitative PCR analyses demonstrated that the overall mRNA expression of insulin/IGF signaling-related genes was mainly impaired in the anterior part of the cerebrum, frontal cortex, and hippocampus, similar to the early stage of sAD. The changes were accompanied by the loss of oligodendrocytes and neurons. The posterior part of the cerebrum did not show degenerative alterations. The present study provides important fundamental information on the icv-STZ monkey model for sAD. These results may help guide future studies using this model for the investigation of pathological mechanisms and the development of drugs for sAD.

摘要

我们之前报道过,脑室注射链脲佐菌素(icv-STZ)的食蟹猴在 FDG-PET 成像中表现出区域性葡萄糖代谢低下,类似于散发性阿尔茨海默病(sAD)的早期阶段。然而,需要对该模型进行分子水平的进一步病理分析,以验证其作为 sAD 可行模型的合理性。两只食蟹猴在第 1、7 和 14 天向小脑延髓池内注射 2mg/kg 的 STZ。两只对照猴给予生理盐水。在注射后 5 个月,检测了对照组和 icv-STZ 处理的食蟹猴前额叶、海马体、后扣带回、楔前叶和枕叶皮质中胰岛素/胰岛素样生长因子(IGF)信号的 9 个上游分子和 4 种细胞类型标志物的基因表达水平。实时定量 PCR 分析表明,胰岛素/IGF 信号相关基因的总体 mRNA 表达主要在前脑、额叶皮质和海马体的前部受损,类似于 sAD 的早期阶段。这些变化伴随着少突胶质细胞和神经元的丢失。后脑的后部没有显示出退行性改变。本研究为 sAD 的 icv-STZ 猴模型提供了重要的基础信息。这些结果可能有助于指导未来使用该模型进行病理机制研究和 sAD 药物开发的研究。

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