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首页> 外文期刊>Journal of Neuroscience Methods >PET measurement of changes in D2/D3 dopamine receptor binding in a nonhuman primate during chronic deep brain stimulation of the bed nucleus of the stria terminalis.
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PET measurement of changes in D2/D3 dopamine receptor binding in a nonhuman primate during chronic deep brain stimulation of the bed nucleus of the stria terminalis.

机译:PET测量在非人类灵长类动物的D2 / D3多巴胺受体结合方面的变化,该刺激是在对末端纹状体床核进行慢性深部脑刺激时产生的。

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PET imaging is a powerful tool for measuring physiological changes in the brain during deep brain stimulation (DBS). In this work, we acquired five PET scans using a highly selective D2/D3 dopamine antagonist, 18F-fallypride, to track changes in dopamine receptor availability, as measured by the distribution volume ratio (DVR), through the course of DBS in the bed nucleus of the stria terminalis (BNST) in a nonhuman primate. METHODS: PET scans were performed on a rhesus monkey with unilateral BNST stimulation during periods of baseline, chronic high frequency (130Hz) and low frequency (50Hz) DBS stimulation, and during a washout period between stimulation periods. A final scan was performed with the electrode stimulation starting 110min into the scan. Whole brain parametric images of (18)F-fallypride DVR were calculated for each condition to track changes in both striatal and extrastriatal D2/D3 availability. RESULTS: The monkey displayed significant increases in receptor binding throughout the brain during DBS relative to baseline for 130 and 50Hz, with changes in DVR of: caudate 42%, 51%; putamen 56%, 57%; thalamus 33%, 49%; substantia nigra 29%, 26%; and prefrontal cortex 28%, 56%, respectively. Washout and post-stimulation scans revealed DVR values close to baseline values. Activating the stimulator midway through the final scan resulted in no statistically significant changes in binding. CONCLUSIONS: PET neuroligand imaging has demonstrated the sensitivity to track changes in dopamine D2/D3 binding during the course of DBS. These methods show great potential for providing insight into the neurochemical consequences of DBS.
机译:PET成像是测量深部脑刺激(DBS)期间脑部生理变化的强大工具。在这项工作中,我们使用高度选择性的D2 / D3多巴胺拮抗剂18F-fallypride进行了五次PET扫描,以跟踪通过床中DBS的过程通过分布体积比(DVR)衡量的多巴胺受体可用性的变化。非人类灵长类动物的终末皮纹(BNST)核。方法:在基线,慢性高频(130Hz)和低频(50Hz)DBS刺激期间以及刺激期间之间的冲洗期间,对单侧BNST刺激的恒河猴进行PET扫描。进行最终扫描,电极刺激从扫描开始110分钟开始。针对每种情况计算(18)F-fallypride DVR的全脑参数图像,以跟踪纹状体和纹状体D2 / D3可用性的变化。结果:在130和50Hz时,猴子在DBS期间相对于基线在整个大脑中的受体结合显着增加,DVR的变化为:尾状42%,51%;尾状42%。壳蛋白56%,57%;丘脑33%,49%;黑质29%,26%;和前额叶皮层分别为28%,56%。冲洗和刺激后扫描显示DVR值接近基线值。在最终扫描的中途激活刺激器,结果绑定的变化无统计学意义。结论:PET神经配体成像已证明在DBS过程中跟踪多巴胺D2 / D3结合变化的敏感性。这些方法显示出提供深入了解DBS神经化学后果的巨大潜力。

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