Litaudon Philippe, Bouillot Caroline, Zimmer Luc, Costes Nicolas, Ravel Nadine
Lyon Neuroscience Research Center, Olfaction: from coding to memory Team, CNRS UMR 5292, INSERM U1028, Université Claude Bernard Lyon 1, 50 Avenue Tony Garnier, 69366, Lyon Cedex, France.
CERMEP-Imagerie du Vivant, 59 Boulevard Pinel, 69677, Bron, France.
Brain Struct Funct. 2017 Jan;222(1):577-586. doi: 10.1007/s00429-016-1235-8. Epub 2016 May 18.
How olfactory cortical areas interpret odor maps evoked in the olfactory bulb and translate odor information into behavioral responses is still largely unknown. Indeed, rat olfactory cortices encompass an extensive network located in the ventral part of the brain, thus complicating the use of invasive functional methods. In vivo imaging techniques that were previously developed for brain activation studies in humans have been adapted for use in rodents and facilitate the non-invasive mapping of the whole brain. In this study, we report an initial series of experiments designed to demonstrate that microPET is a powerful tool to investigate the neural processes underlying odor-induced behavioral response in a large-scale olfactory neuronal network. After the intravenous injection of [F]Fluorodeoxyglucose ([F]FDG), awake rats were placed in a ventilated Plexiglas cage for 50 min, where odorants were delivered every 3 min for a 10-s duration in a random order. Individual behavioral responses to odor were classified into categories ranging from 1 (head movements associated with a short sniffing period in response to a few stimulations) to 4 (a strong reaction, including rearing, exploring and sustained sniffing activity, to several stimulations). After [F]FDG uptake, rats were anesthetized to perform a PET scan. This experimental session was repeated 2 weeks later using the same animals without odor stimulation to assess the baseline level of activation in each individual. Two voxel-based statistical analyses (SPM 8) were performed: (1) a two-sample paired t test analysis contrasting baseline versus odor scan and (2) a correlation analysis between voxel FDG activity and behavioral score. As expected, the contrast analysis between baseline and odor session revealed activations in various olfactory cortical areas. Significant increases in glucose metabolism were also observed in other sensory cortical areas involved in whisker movement and in several modules of the cerebellum involved in motor and sensory function. Correlation analysis provided new insight into these results. [F]FDG uptake was correlated with behavioral response in a large part of the anterior piriform cortex and in some lobules of the cerebellum, in agreement with the previous data showing that both piriform cortex and cerebellar activity in humans can be driven by sniffing activity, which was closely related to the high behavioral scores observed in our experiment. The present data demonstrate that microPET imaging offers an original perspective for rat behavioral neuroimaging.
嗅觉皮层区域如何解读嗅球中诱发的气味图谱,并将气味信息转化为行为反应,目前仍 largely 未知。实际上,大鼠嗅觉皮层包含位于大脑腹侧的广泛网络,这使得侵入性功能方法的使用变得复杂。先前为人类大脑激活研究开发的体内成像技术已被改编用于啮齿动物,并有助于对全脑进行非侵入性图谱绘制。在本研究中,我们报告了一系列初步实验,旨在证明微型正电子发射断层扫描(microPET)是一种强大的工具,可用于研究大规模嗅觉神经元网络中气味诱导行为反应背后的神经过程。静脉注射[F]氟脱氧葡萄糖([F]FDG)后,将清醒的大鼠置于通风的有机玻璃笼中 50 分钟,每隔 3 分钟以随机顺序输送气味剂,持续 10 秒。对气味的个体行为反应分为从 1(对少数刺激做出短嗅期相关头部运动)到 4(对几种刺激做出强烈反应,包括站立、探索和持续嗅探活动)的类别。在[F]FDG 摄取后,将大鼠麻醉以进行 PET 扫描。两周后使用相同动物重复此实验环节,不进行气味刺激,以评估每个个体的基线激活水平。进行了两种基于体素的统计分析(SPM 8):(1)对比基线与气味扫描的两样本配对 t 检验分析,以及(2)体素 FDG 活性与行为评分之间的相关性分析。正如预期的那样,基线与气味阶段之间的对比分析揭示了各个嗅觉皮层区域的激活。在参与胡须运动的其他感觉皮层区域以及参与运动和感觉功能的小脑的几个模块中也观察到葡萄糖代谢显著增加。相关性分析为这些结果提供了新的见解。[F]FDG 摄取与大部分前梨状皮层和小脑的一些小叶中的行为反应相关,这与先前的数据一致,即人类的梨状皮层和小脑活动都可以由嗅探活动驱动,这与我们实验中观察到的高行为评分密切相关。目前的数据表明,微型正电子发射断层扫描成像为大鼠行为神经成像提供了一个全新的视角。