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Detection of Neuroinflammation in a Rat Model of Subarachnoid Hemorrhage Using 18FDPA-714 PET Imaging

机译:18F DPA-714 PET成像在蛛网膜下腔出血大鼠模型中检测神经炎症

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摘要

Subarachnoid hemorrhage (SAH) can lead to delayed cerebral ischemia, which increases the rate of morbidity and mortality. The detection of microglial activation may serve as a biomarker for the identification of patients at risk of this deleterious consequence. We assessed this hypothesis in a rat model of SAH in which the exploration of neuroinflammation related to microglial activation was correlated with the degree of bleeding. We used the rat filament model and evaluated (at 48 hours postsurgery) the intensity of neuroinflammation using positron emission tomography (PET) imaging with the 18-kDa translocator protein (TSPO) tracer [18F]DPA-714, quantitative autoradiography with [3H]PK-11195, and SAH grade by postmortem brain picture. High SAH grades were strongly and positively correlated with in vivo PET imaging of TSPO in the cortex and striatum. In addition, a positive correlation was found in the cortex in TSPO, with densities determined by imaging and autoradiographic approaches. Qualitative immunofluorescence studies indicated that overexpression of TSPO was linked to astrocytic/microglial activation. In this model, PET imaging of TSPO using [18F]DPA-714 appeared to be a relevant index of the degree of bleeding, indicating that this imaging method could be used in human patients to improve the management of patients with SAH.
机译:蛛网膜下腔出血(SAH)可能导致脑缺血延迟,从而增加发病率和死亡率。小胶质细胞活化的检测可以用作生物标志物,以鉴定处于这种有害后果风险中的患者。我们在SAH大鼠模型中评估了这一假设,在该模型中,与小胶质细胞活化相关的神经炎症的探索与出血程度相关。我们使用大鼠细丝模型,并在手术后48小时使用正电子发射断层扫描(PET)成像和18 kDa转运蛋白(TSPO)示踪剂[ 18 F] DPA- 714,[ 3 H] PK-11195的定量放射自显影照片,以及根据尸体脑照片划分的SAH等级。高SAH等级与皮层和纹状体中TSPO的体内PET成像密切相关且呈正相关。另外,在TSPO的皮质中发现正相关,其密度通过成像和放射自显影方法确定。定性免疫荧光研究表明,TSPO的过度表达与星形胶质细胞/小胶质细胞活化有关。在该模型中,使用[ 18 F] DPA-714的TSPO的PET成像似乎是出血程度的相关指标,表明该成像方法可用于人类患者以改善管理SAH患者。

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