fMRI BOLD 对电影刺激的反应及其与哮喘和健康中呼气一氧化氮的关系。

Psychophysiology Pub Date : 2024-05-01 Epub Date: 2024-02-10 DOI:10.1111/psyp.14513
Thomas Ritz, Juliet L Kroll, David A Khan, Uma S Yezhuvath, Sina Aslan, Amy Pinkham, David Rosenfield, E Sherwood Brown
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引用次数: 0

摘要

人们对哮喘患者中枢神经系统(CNS)对情绪刺激的反应知之甚少。由于过敏性免疫过程,哮喘患者呼出气体中的一氧化氮(FENO)会升高,但已知内源性一氧化氮也能调节中枢神经系统的活动。我们测量了 31 名参与者(15 名哮喘患者)的 fMRI 血氧依赖性(BOLD)脑激活对负性(血液注射损伤主题)和中性电影的影响。我们对与中枢适应控制、威胁处理或显著性网络相关的关键区域进行了兴趣区分析,包括背外侧前额叶皮层(PFC)、前脑岛、背侧前扣带回皮层(dACC)、杏仁核、腹侧纹状体、腹侧被盖区和输导周围灰质,以及自上而下调节情绪的腹外侧和腹内侧前额叶皮层。与中性电影相比,两组受试者的左侧前脑岛和双侧腹内侧前脑功能区从定点跨基线开始的 BOLD 失活程度较低,而在电影与恢复阶段,包括纺锤形回在内的其他一些区域的 BOLD 失活程度也较低。与健康对照组相比,哮喘患者在拍片过程中的失活较少,失活后的恢复也较少。PCO2 的变化并不能解释这些发现。一般来说,FENO 与 BOLD 激活呈正相关,但在健康对照组中更明显,在中性电影处理中更有可能。因此,哮喘与大脑各区域对胶片刺激的处理改变有关,而不局限于中央适应控制、威胁处理或显著性网络。较高水平的氮氧化物似乎促进了中枢神经系统的活动,但仅适用于健康对照组,这可能是由于过敏对 FENO 的掩蔽效应。
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fMRI BOLD responses to film stimuli and their association with exhaled nitric oxide in asthma and health.

Little is known about central nervous system (CNS) responses to emotional stimuli in asthma. Nitric oxide in exhaled breath (FENO) is elevated in asthma due to allergic immune processes, but endogenous nitric oxide is also known to modulate CNS activity. We measured fMRI blood oxygen-dependent (BOLD) brain activation to negative (blood-injection-injury themes) and neutral films in 31 participants (15 with asthma). Regions-of-interest analysis was performed on key areas relevant to central adaptive control, threat processing, or salience networks, with dorsolateral prefrontal cortex (PFC), anterior insula, dorsal anterior cingulate cortex (dACC), amygdala, ventral striatum, ventral tegmentum, and periaqueductal gray, as well as top-down modulation of emotion, with ventrolateral and ventromedial PFC. Both groups showed less BOLD deactivation from fixation cross-baseline in the left anterior insula and bilateral ventromedial PFC for negative than neutral films, and for an additional number of areas, including the fusiform gyrus, for film versus recovery phases. Less deactivation during films followed by less recovery from deactivation was found in asthma compared to healthy controls. Changes in PCO2 did not explain these findings. FENO was positively related to BOLD activation in general, but more pronounced in healthy controls and more likely in neutral film processing. Thus, asthma is associated with altered processing of film stimuli across brain regions not limited to central adaptive control, threat processing, or salience networks. Higher levels of NO appear to facilitate CNS activity, but only in healthy controls, possibly due to allergy's masking effects on FENO.

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