Service Hospitalier Frédéric Joliot, CEA, DSV, I²BM, Orsay, France.
Eur J Nucl Med Mol Imaging. 2011 Mar;38(3):509-14. doi: 10.1007/s00259-010-1628-5. Epub 2010 Oct 9.
Neuroinflammation is involved in neurological disorders through the activation of microglial cells. Imaging of neuroinflammation with radioligands for the translocator protein (18 kDa) (TSPO) could prove to be an attractive biomarker for disease diagnosis and therapeutic evaluation. The indoleacetamide-derived 7-chloro-N,N,5-trimethyl-4-oxo-3-phenyl-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-acetamide, SSR180575, is a selective high-affinity TSPO ligand in human and rodents with neuroprotective effects.
Here we report the radiolabelling of SSR180575 with (11)C and in vitro and in vivo imaging in an acute model of neuroinflammation in rats.
The image contrast and the binding of [(11)C]SSR180575 are higher than that obtained with the isoquinoline-based TSPO radioligand, [(11)C]PK11195. Competition studies demonstrate that [(11)C]SSR180575 has high specific binding for the TSPO.
[(11)C]SSR180575 is the first PET radioligand for the TSPO based on an indoleacetamide scaffold designed for imaging neuroinflammation in animal models and in the clinic.
神经炎症通过小胶质细胞的激活参与神经紊乱。用转位蛋白(18 kDa)(TSPO)的放射性配体对神经炎症进行成像,可能成为疾病诊断和治疗评估的有吸引力的生物标志物。吲哚乙酰胺衍生的 7-氯-N,N,5-三甲基-4-氧代-3-苯基-3,5-二氢-4H-吡咯嗪并[4,5-b]吲哚-1-乙酰胺,SSR180575,是一种在人和啮齿动物中具有神经保护作用的选择性高亲和力 TSPO 配体。
在这里,我们报告了 SSR180575 与 (11)C 的放射性标记以及在大鼠急性神经炎症模型中的体外和体内成像。
与基于异喹啉的 TSPO 放射性配体 [(11)C]PK11195 相比,[(11)C]SSR180575 的图像对比度和结合更高。竞争研究表明,[(11)C]SSR180575 对 TSPO 具有高特异性结合。
[(11)C]SSR180575 是基于吲哚乙酰胺支架设计的用于在动物模型和临床中成像神经炎症的第一个 TSPO PET 放射性配体。