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Quantification of Brain Access of Exendin-4 in the C57BL Mouse Model by SPIM Fluorescence Imaging and the Allen Mouse Brain Reference Model

机译:通过Spim荧光成像和艾伦小鼠脑参考模型的C57BL小鼠模型中Exendin-4的大脑进入的定量

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With the recent advance in 3D microscopy such as Single Plane Illumination Microscopy (SPIM) it is possible to obtain high resolution image volumes of the entire mouse brain. These data can be used to study the access of several peptides such as the glucagon-like peptide-1 (GLP-1) analogue Exendin-4, into the brain with the aim of developing medication for obesity. To investigate mode of action of the medication it is important to identify the specific anatomical brain nuclei that are targeted by the compound. Such segmentations can be obtained using an annotated digital brain atlas. We construct a SPIM brain atlas based on the Allen mouse brain 3D reference model and use it to analyze the access of peripherally injected Exendin-4 into the brain compared to a negative control group. The constructed atlas consists of an average SPIM volume obtained from eight C57BL mouse brains using group-wise registration. A cross-modality registration is performed between the constructed average volume and the Allen mouse brain reference model to allow propagation of annotations to the SPIM average brain. Finally, manual corrections of the annotations are performed and validated by visual inspection. The study shows that Exendin-4 have access to brain regions such as the arcuate hypothalamic nucleus and the nucleus of the solitary tract, which are areas involved in regulating food intake.
机译:随着3D显微镜的最近进步,例如单个平面照明显微镜(SPIM),可以获得整个小鼠脑的高分辨率图像体积。这些数据可用于研究诸如胰高血糖素样肽-1(GLP-1)类似物Exendin-4的几种肽的进入,其目的是肥胖的药物。研究药物的作用方式,重要的是鉴定由化合物靶向的特定解剖脑核。可以使用带注释的数字脑图集获得这种分割。我们基于艾伦小鼠脑3D参考模型构建尖端脑地图集,并与阴性对照组相比,使用它来分析外周注入的exendin-4进入大脑的进入。构造的阿特拉斯包括使用组织登记的八个C57BL鼠标大脑获得的平均尖端体积。在构造的平均体积和艾伦小鼠脑参考模型之间进行横向形态注册,以允许注释传播到尖端平均大脑。最后,通过目视检查执行和验证注释的手动校正。该研究表明,Exendin-4可以访问脑区,例如弓形下丘脑核和孤立的细胞核,这是参与调节食物摄入的地区。

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