He Ji-Wei, Liu Hanli, Peng Yuan Bo
Departments of Psychology, University of Texas at Arlington, Arlington, TX 76019, USA.
Department of Neurological Surgery, University of California San Francisco, 1700 Owens Street, San Francisco, CA 94158, USA.
Brain Sci. 2015 Sep 29;5(4):400-18. doi: 10.3390/brainsci5040400.
Neuroimaging technologies with an exceptional spatial resolution and noninvasiveness have become a powerful tool for assessing neural activity in both animals and humans. However, the effectiveness of neuroimaging for pain remains unclear partly because the neurovascular coupling during pain processing is not completely characterized. Our current work aims to unravel patterns of neurovascular parameters in pain processing. A novel fiber-optic method was used to acquire absolute values of regional oxy- (HbO) and deoxy-hemoglobin concentrations, oxygen saturation rates (SO₂), and the light-scattering coefficients from the spinal cord and primary somatosensory cortex (SI) in 10 rats. Brief mechanical and electrical stimuli (ranging from innocuous to noxious intensities) as well as a long-lasting noxious stimulus (formalin injection) were applied to the hindlimb under pentobarbital anesthesia. Interhemispheric comparisons in the spinal cord and SI were used to confirm functional activation during sensory processing. We found that all neurovascular parameters showed stimulation-induced changes; however, patterns of changes varied with regions and stimuli. Particularly, transient increases in HbO and SO₂ were more reliably attributed to brief stimuli, whereas a sustained decrease in SO₂ was more reliably attributed to formalin. Only the ipsilateral SI showed delayed responses to brief stimuli. In conclusion, innocuous and noxious stimuli induced significant neurovascular responses at critical centers (e.g., the spinal cord and SI) along the somatosensory pathway; however, there was no single response pattern (as measured by amplitude, duration, lateralization, decrease or increase) that was able to consistently differentiate noxious stimuli. Our results strongly suggested that the neurovascular response patterns differ between brief and long-lasting noxious stimuli, and can also differ between the spinal cord and SI. Therefore, a use of multiple-parameter strategy tailored by stimulus modality (brief or long-lasting) as well as region-dependent characteristics may be more effective in detecting pain using neuroimaging technologies.
具有卓越空间分辨率和非侵入性的神经成像技术已成为评估动物和人类神经活动的强大工具。然而,神经成像对疼痛的有效性仍不明确,部分原因是疼痛处理过程中的神经血管耦合尚未完全明确。我们目前的工作旨在揭示疼痛处理过程中神经血管参数的模式。采用一种新型光纤方法获取了10只大鼠脊髓和初级体感皮层(SI)的局部氧合血红蛋白(HbO)和脱氧血红蛋白浓度、氧饱和度(SO₂)以及光散射系数的绝对值。在戊巴比妥麻醉下,对后肢施加短暂的机械和电刺激(强度从无害到有害)以及持续的有害刺激(福尔马林注射)。通过脊髓和SI的半球间比较来确认感觉处理过程中的功能激活。我们发现所有神经血管参数均显示出刺激诱导的变化;然而,变化模式因区域和刺激而异。特别是,HbO和SO₂的短暂增加更可靠地归因于短暂刺激,而SO₂的持续下降更可靠地归因于福尔马林。只有同侧SI对短暂刺激表现出延迟反应。总之,无害和有害刺激在体感通路的关键中枢(如脊髓和SI)诱导了显著的神经血管反应;然而,没有单一的反应模式(通过幅度、持续时间、偏侧化、降低或增加来衡量)能够始终如一地区分有害刺激。我们的结果强烈表明,短暂和持续有害刺激之间的神经血管反应模式不同,脊髓和SI之间也可能不同。因此,根据刺激方式(短暂或持续)以及区域依赖性特征量身定制的多参数策略,可能在使用神经成像技术检测疼痛方面更有效。