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[F]AlF-NOTA-MAL-Cys-exendin-4 可检测大鼠 GLP-1R 表达随年龄变化。

Age-related change of GLP-1R expression in rats can be detected by [F]AlF-NOTA-MAL-Cys-exendin-4.

机构信息

Key Laboratory of Nuclear Medicine, Ministry of Health, Jiangsu Key Laboratory of Molecular Nuclear Medicine, Jiangsu Institute of Nuclear Medicine, Wuxi 214063, Jiangsu, China.

The First School of Clinical Medicine, Nanjing Medical University, Nanjing 210029, Jiangsu, China.

出版信息

Brain Res. 2018 Nov 1;1698:213-219. doi: 10.1016/j.brainres.2018.08.022. Epub 2018 Aug 23.

Abstract

The glucagon-like peptide-1 receptor (GLP-1R) has been demonstrated as a potential therapeutic target for some neurological diseases such as Alzheimer's disease (AD), Parkinson's disease (PD), and stroke. Besides, its distribution and density in brain regions are closely associated with cognition, motor function, learning and memory. Given the relationship between age and these neurological diseases, we firstly examined the influences of age on GLP-1R expression using [F]AlF-NOTA-MAL-Cys-exendin-4 microPET imaging. The image showed that GLP-1R expression in nearly all regions of the brain of aged rats was evidently lower than that of normal rats. Significant differences were found in olfactory, striatum, hypothalamus, substantial nigra, and hippocampus, which have inseparable relations with some mental and neurological diseases such as PD and AD. Data obtained from biodistribution and immunohistochemistry staining also confirmed the image results. Taken together, these results illustrated decreased expression of GLP-1R in the brain of aged rats can be detected by [F]AlF-NOTA-MAL-Cys-exendin-4, which implied GLP-1R as a reliable target and GLP-1R PET imaging could be a promising technology in the field of neurological diseases.

摘要

胰高血糖素样肽-1 受体 (GLP-1R) 已被证明是治疗某些神经疾病(如阿尔茨海默病 (AD)、帕金森病 (PD) 和中风)的潜在治疗靶点。此外,其在大脑区域的分布和密度与认知、运动功能、学习和记忆密切相关。鉴于年龄与这些神经疾病之间的关系,我们首先使用 [F]AlF-NOTA-MAL-Cys-exendin-4 microPET 成像来检查年龄对 GLP-1R 表达的影响。图像显示,老年大鼠大脑几乎所有区域的 GLP-1R 表达明显低于正常大鼠。在嗅球、纹状体、下丘脑、黑质和海马等与 PD 和 AD 等一些精神和神经疾病密切相关的区域,差异显著。从生物分布和免疫组织化学染色获得的数据也证实了图像结果。总之,这些结果表明,[F]AlF-NOTA-MAL-Cys-exendin-4 可检测到老年大鼠大脑中 GLP-1R 表达减少,这表明 GLP-1R 是一个可靠的靶点,GLP-1R PET 成像可能是神经疾病领域的一项有前途的技术。

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