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Neuroimaging in Animal Seizure Models with18FDG-PET

机译:用18FDG-PET在动物癫痫发作模型中进行神经成像

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Small animal neuroimaging has become increasingly available to researchers, expanding the breadth of questions studied with these methods. Applying these noninvasive techniques to the open questions underlying epileptogenesis is no exception. A major advantage of small animal neuroimaging is its translational appeal. Studies can be well controlled and manipulated, examining the living brain in the animal before, during, and after the disease onset or disease treatment. The results can also be compared to data collected on human patients. Over the past decade, we and others have explored metabolic patterns in animal models of epilepsy to gain insight into the circuitry underlying development of the disease. In this paper, we provide technical details on how metabolic imaging that uses 2-deoxy-2[18F]fluoro-D-glucose (18FDG) and positron emission tomography (PET) is performed and explain the strengths and limitations of these studies. We will also highlight recent advances toward understanding epileptogenesis through small animal imaging.
机译:小型动物神经影像已越来越多地提供给研究人员,从而扩大了使用这些方法研究的问题的范围。将这些非侵入性技术应用于癫痫发生的开放性问题也不例外。小动物神经影像学的主要优点是其翻译吸引力。可以很好地控制和操纵研究,在疾病发作或疾病治疗之前,之中和之后检查动物的活脑。还可将结果与人类患者收集的数据进行比较。在过去的十年中,我们和其他人探索了癫痫动物模型中的代谢模式,以深入了解疾病发展的潜在电路。在本文中,我们提供了有关如何使用2-deoxy-2 [18F]氟-D-葡萄糖(18FDG)和正电子发射断层扫描(PET)进行代谢成像的技术细节,并解释了这些研究的优势和局限性。我们还将重点介绍通过小动物成像了解癫痫发生的最新进展。

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