警觉猕猴初级视觉皮层黄蛋白荧光与血流动力学反应的空间关系

Frontiers in neuroenergetics Pub Date : 2010-06-03 eCollection Date: 2010-01-01 DOI:10.3389/fnene.2010.00006
Yevgeniy B Sirotin, Aniruddha Das
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引用次数: 22

摘要

与常用的血流动力学信号相比,黄蛋白荧光成像(Flavoprotein fluorescence imaging, FFI)是一种新型的内在光信号,由于其与局部代谢的关系更密切,在神经科学研究中逐渐成为一种有价值的成像工具。我们开发了一种在警觉猴子初级视觉皮层(V1)进行FFI成像的技术。由于神经血管耦合的性质,已知血流动力学信号会传播到代谢活动位点之外。为了确定FFI信号是否能在警觉动物中提供更集中的皮质活动测量,我们比较了执行简单注视任务的猕猴的FFI和血流动力学点扩散(即对最小视觉刺激的反应)以及V1上的功能映射信号。FFI反应是双相的,早期和局部荧光增加,然后是延迟和空间范围更广的荧光减少。正如预期的那样,早期荧光增加,表明局部氧化代谢增加,比同时观察到的血流动力学反应稍窄。然而,后期FFI的下降范围比血流动力学反应更广泛,并且在视觉刺激停止之前就开始了,这表明荧光信号的两个阶段背后的不同机制。FFI作图信号没有血管伪影,其振幅与血流动力学作图信号相当。这些结果表明,在警觉动物中,FFI反应可能是比血流动力学反应更局部和直接的皮质代谢指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Spatial Relationship between Flavoprotein Fluorescence and the Hemodynamic Response in the Primary Visual Cortex of Alert Macaque Monkeys.

Spatial Relationship between Flavoprotein Fluorescence and the Hemodynamic Response in the Primary Visual Cortex of Alert Macaque Monkeys.

Spatial Relationship between Flavoprotein Fluorescence and the Hemodynamic Response in the Primary Visual Cortex of Alert Macaque Monkeys.

Spatial Relationship between Flavoprotein Fluorescence and the Hemodynamic Response in the Primary Visual Cortex of Alert Macaque Monkeys.

Flavoprotein fluorescence imaging (FFI) is a novel intrinsic optical signal that is steadily gaining ground as a valuable imaging tool in neuroscience research due to its closer relationship with local metabolism relative to the more commonly used hemodynamic signals. We have developed a technique for FFI imaging in the primary visual cortex (V1) of alert monkeys. Due to the nature of neurovascular coupling, hemodynamic signals are known to spread beyond the locus of metabolic activity. To determine whether FFI signals could provide a more focal measure of cortical activity in alert animals, we compared FFI and hemodynamic point spreads (i.e. responses to a minimal visual stimulus) and functional mapping signals over V1 in macaques performing simple fixation tasks. FFI responses were biphasic, with an early and focal fluorescence increase followed by a delayed and spatially broader fluorescence decrease. As expected, the early fluorescence increase, indicating increased local oxidative metabolism, was somewhat narrower than the simultaneously observed hemodynamic response. However, the later FFI decrease was broader than the hemodynamic response and started prior to the cessation of visual stimulation suggesting different mechanisms underlying the two phases of the fluorescence signal. FFI mapping signals were free of vascular artifacts and comparable in amplitude to hemodynamic mapping signals. These results indicate that the FFI response may be a more local and direct indicator of cortical metabolism than the hemodynamic response in alert animals.

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