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人类视觉皮层的偏心率映射,用于评估功能性T1ρ映射的时间动态变化。

Eccentricity mapping of the human visual cortex to evaluate temporal dynamics of functional T1ρ mapping.

作者信息

Heo Hye-Young, Wemmie John A, Johnson Casey P, Thedens Daniel R, Magnotta Vincent A

机构信息

1] Department of Radiology, University of Iowa, Iowa City, Iowa, USA [2] Department of Biomedical Engineering, University of Iowa, Iowa City, Iowa, USA.

1] Department of Psychiatry, University of Iowa, Iowa City, Iowa, USA [2] Department of Neurosurgery, University of Iowa, Iowa City, Iowa, USA [3] Department of Veterans Affairs Medical Center, Iowa City, USA.

出版信息

J Cereb Blood Flow Metab. 2015 Jul;35(7):1213-9. doi: 10.1038/jcbfm.2015.94. Epub 2015 May 13.

Abstract

Recent experiments suggest that T1 relaxation in the rotating frame (T(1ρ)) is sensitive to metabolism and can detect localized activity-dependent changes in the human visual cortex. Current functional magnetic resonance imaging (fMRI) methods have poor temporal resolution due to delays in the hemodynamic response resulting from neurovascular coupling. Because T(1ρ) is sensitive to factors that can be derived from tissue metabolism, such as pH and glucose concentration via proton exchange, we hypothesized that activity-evoked T(1ρ) changes in visual cortex may occur before the hemodynamic response measured by blood oxygenation level-dependent (BOLD) and arterial spin labeling (ASL) contrast. To test this hypothesis, functional imaging was performed using T(1ρ), BOLD, and ASL in human participants viewing an expanding ring stimulus. We calculated eccentricity phase maps across the occipital cortex for each functional signal and compared the temporal dynamics of T(1ρ) versus BOLD and ASL. The results suggest that T(1ρ) changes precede changes in the two blood flow-dependent measures. These observations indicate that T(1ρ) detects a signal distinct from traditional fMRI contrast methods. In addition, these findings support previous evidence that T(1ρ) is sensitive to factors other than blood flow, volume, or oxygenation. Furthermore, they suggest that tissue metabolism may be driving activity-evoked T(1ρ) changes.

摘要

最近的实验表明,旋转坐标系中的T1弛豫(T(1ρ))对新陈代谢敏感,并且能够检测人类视觉皮层中局部的活动依赖性变化。由于神经血管耦合导致的血液动力学反应延迟,当前的功能磁共振成像(fMRI)方法具有较差的时间分辨率。因为T(1ρ)对可从组织新陈代谢中得出的因素敏感,例如通过质子交换的pH值和葡萄糖浓度,我们推测视觉皮层中由活动引起的T(1ρ)变化可能发生在通过血氧水平依赖(BOLD)和动脉自旋标记(ASL)对比测量的血液动力学反应之前。为了验证这一假设,在观看扩展环形刺激的人类受试者中使用T(1ρ)、BOLD和ASL进行了功能成像。我们为每个功能信号计算了枕叶皮层的偏心率相位图,并比较了T(1ρ)与BOLD和ASL的时间动态变化。结果表明,T(1ρ)的变化先于两种依赖血流的测量指标的变化。这些观察结果表明,T(1ρ)检测到的信号不同于传统的fMRI对比方法。此外,这些发现支持了先前的证据,即T(1ρ)对血流、血容量或氧合以外的因素敏感。此外,它们表明组织新陈代谢可能驱动了由活动引起的T(1ρ)变化。

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