Cognitive Systems Group, Discipline of Psychiatry, School of Medicine, Trinity College Dublin, Dublin, Ireland.
Neurobiol Aging. 2013 Mar;34(3):809-21. doi: 10.1016/j.neurobiolaging.2012.07.006. Epub 2012 Aug 11.
Arousal and valence play key roles in emotional perception, with normal aging leading to changes in the neural substrates supporting valence processing. The objective of this study was to investigate normal age-related changes in the neural substrates of emotional arousal processing. Twenty-three young and 23 older, healthy women underwent functional magnetic resonance imaging as they viewed images which were neutral or positive in valence and which varied in arousal level from low to high. Using a parametric modulation approach, we examined how the blood oxygen-level dependent signal varied with single trial subjective ratings of valence and arousal, and whether this differed with age. In accordance with previous studies we found that the older group showed greater activation in response to positive valence, in the left amygdala, left middle temporal gyrus and right lingual gyrus. In contrast however, they showed reduced reactivity to emotional arousal, in occipital and temporal visual cortices bilaterally, the left inferior parietal cortex, and the supplementary motor area bilaterally. This study represents the first of its kind to clearly dissociate how aging affects the neural correlates of emotional arousal and valence. The changes in arousal processing may in part be mediated by the functional reorganization evident in the aging brain, such as reduced activation of the posterior cortices as described by the posterior-anterior shift in ageing (PASA) effect.
唤醒度和效价在情绪感知中起着关键作用,正常衰老会导致支持效价加工的神经基质发生变化。本研究旨在探讨情绪唤醒处理的神经基质随正常年龄变化的情况。23 名年轻和 23 名年长、健康的女性接受了功能磁共振成像,当她们观看效价中性或积极、唤醒水平从低到高变化的图像时。我们使用参数调制方法,研究了血液氧水平依赖信号如何随单一试验主观效价和唤醒评分而变化,以及这种变化是否因年龄而异。与之前的研究一致,我们发现老年组在左杏仁核、左中颞叶和右舌回对正性效价的反应中表现出更大的激活。然而,与年轻组相比,他们在双侧枕叶和颞叶视觉皮层、左顶下小叶和双侧辅助运动区对情绪唤醒的反应性降低。这项研究首次清楚地区分了衰老如何影响情绪唤醒和效价的神经相关性。唤醒处理的变化可能部分是由衰老大脑中明显的功能重组介导的,例如如后部皮层的激活减少,正如后部-前部转移老化(PASA)效应所描述的那样。