Clewett David, Sakaki Michiko, Nielsen Shawn, Petzinger Giselle, Mather Mara
Neuroscience Graduate Program, University of Southern California, USA.
School of Psychology and Clinical Language Sciences, University of Reading, UK.
Neurobiol Learn Mem. 2017 Jan;137:1-14. doi: 10.1016/j.nlm.2016.10.017. Epub 2016 Nov 2.
Arousal's selective effects on cognition go beyond the simple enhancement of emotional stimuli, sometimes enhancing and other times impairing processing of proximal neutral information. Past work shows that arousal impairs encoding of subsequent neutral stimuli regardless of their top-down priority via the engagement of β-adrenoreceptors. In contrast, retrograde amnesia induced by emotional arousal can flip to enhancement when preceding neutral items are prioritized in top-down attention. Whether β-adrenoreceptors also contribute to this retrograde memory enhancement of goal-relevant neutral stimuli is unclear. In this pharmacological study, we administered 40mg of propranolol or 40mg of placebo to healthy young adults to examine whether emotional arousal's bidirectional effects on declarative memory relies on β-adrenoreceptor activation. Following pill intake, participants completed an emotional oddball task in which they were asked to prioritize a neutral object appearing just before an emotional or neutral oddball image within a sequence of 7 neutral objects. Under placebo, emotional oddballs impaired memory for lower priority oddball+1 objects but had no effect on memory for high priority oddball-1 objects. Propranolol blocked this anterograde amnesic effect of arousal. Emotional oddballs also enhanced selective memory trade-offs significantly more in the placebo than drug condition, such that high priority oddball-1 objects were more likely to be remembered at the cost of their corresponding lower priority oddball+1 objects under arousal. Lastly, those who recalled more high priority oddball-1 objects preceding an emotional versus neutral oddball image showed greater increases in salivary alpha-amylase, a biomarker of noradrenergic system activation, across the task. Together these findings suggest that different noradrenergic mechanisms contribute to the anterograde and retrograde mnemonic effects of arousal on proximal neutral memoranda.
唤醒对认知的选择性影响不仅仅局限于对情绪刺激的简单增强,有时会增强,而有时则会损害对近端中性信息的处理。过去的研究表明,无论中性刺激的自上而下的优先级如何,唤醒都会通过β-肾上腺素能受体的参与损害后续中性刺激的编码。相比之下,当在自上而下的注意力中对先前的中性项目进行优先级排序时,由情绪唤醒引起的逆行性遗忘可以转变为增强。尚不清楚β-肾上腺素能受体是否也有助于与目标相关的中性刺激的这种逆行性记忆增强。在这项药理学研究中,我们给健康的年轻成年人服用40毫克普萘洛尔或40毫克安慰剂,以检查情绪唤醒对陈述性记忆的双向影响是否依赖于β-肾上腺素能受体激活。服药后,参与者完成了一项情绪oddball任务,在该任务中,他们被要求在7个中性物体的序列中,优先处理出现在情绪或中性oddball图像之前的一个中性物体。在安慰剂条件下,情绪oddball会损害对较低优先级oddball+1物体的记忆,但对高优先级oddball-1物体的记忆没有影响。普萘洛尔阻断了唤醒的这种顺行性遗忘效应。情绪oddball在安慰剂组中比药物组更显著地增强了选择性记忆权衡,因此在唤醒状态下,高优先级oddball-1物体更有可能被记住,而以相应的低优先级oddball+1物体为代价。最后,那些在情绪oddball图像之前回忆起更多高优先级oddball-1物体的人,在整个任务中唾液α-淀粉酶(去甲肾上腺素能系统激活生物标志物)的增加幅度更大。这些发现共同表明,不同的去甲肾上腺素能机制促成了唤醒对近端中性记忆的顺行性和逆行性记忆效应。