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转位蛋白(18kDa)正电子发射断层扫描成像作为癫痫神经炎症的生物标志物。

Translocator protein (18 kDa) positron emission tomography imaging as a biomarker of neuroinflammation in epilepsy.

机构信息

Department of Neurology, National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.

Department of Nuclear Medicine, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.

出版信息

Neurol Sci. 2024 Nov;45(11):5201-5211. doi: 10.1007/s10072-024-07648-9. Epub 2024 Jun 16.

Abstract

Increasing evidence indicate that neuroinflammation triggered by glial cells plays a significant role in epileptogenesis. To this effect, the overexpression of translocator protein 18 kDa (TSPO) in activated microglia and astrocytes has been identified as an inflammatory biomarker in epilepsy. It is now possible to quantify neuroinflammation using non-invasive positron emission tomography (PET) imaging of TSPO. With the advancement of radiotracers, TSPO PET has become an innovative tool in elucidating the "neuroinflammatory machinery" of drug-resistant epilepsy. Furthermore, TSPO PET has demonstrated potential in detecting MRI-negative epileptogenic zones (EZ) and provided an innovative perspective in epileptic medical treatment. This manuscript presents a comprehensive exploration of the neuroinflammatory mechanisms of epilepsy, alongside a thorough review of TSPO PET studies conducted in clinical and preclinical settings. The primary objective is to deepen our understanding of epilepsy progression and to establish TSPO PET as an effective monitoring tool for treatment efficacy.

摘要

越来越多的证据表明,神经胶质细胞引发的神经炎症在癫痫发生中起着重要作用。为此,在激活的小胶质细胞和星形胶质细胞中 TSPO 的过表达已被确定为癫痫的炎症生物标志物。现在可以使用 TSPO 的非侵入性正电子发射断层扫描 (PET) 成像来定量神经炎症。随着示踪剂的进步,TSPO PET 已成为阐明耐药性癫痫“神经炎症机制”的创新工具。此外,TSPO PET 已证明在检测 MRI 阴性致痫区 (EZ) 方面具有潜力,并为癫痫治疗提供了创新视角。本文全面探讨了癫痫的神经炎症机制,并对临床和临床前环境中进行的 TSPO PET 研究进行了全面回顾。主要目的是加深我们对癫痫进展的理解,并将 TSPO PET 确立为治疗效果的有效监测工具。

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