Centre for Chronobiology, University Psychiatric Clinics Basel, Wilhelm-Klein Strasse 27, 4002, Basel, Switzerland.
Transfaculty Research Platform Molecular and Cognitive Neurosciences, University of Basel, Basel, Switzerland.
Sci Rep. 2023 Jan 18;13(1):1002. doi: 10.1038/s41598-022-26808-5.
Acute caffeine intake has been found to increase working memory (WM)-related brain activity in healthy adults without improving behavioral performances. The impact of daily caffeine intake-a ritual shared by 80% of the population worldwide-and of its discontinuation on working memory and its neural correlates remained unknown. In this double-blind, randomized, crossover study, we examined working memory functions in 20 young healthy non-smokers (age: 26.4 ± 4.0 years; body mass index: 22.7 ± 1.4 kg/m; and habitual caffeine intake: 474.1 ± 107.5 mg/day) in a 10-day caffeine (150 mg × 3 times/day), a 10-day placebo (3 times/day), and a withdrawal condition (9-day caffeine followed by 1-day placebo). Throughout the 10th day of each condition, participants performed four times a working memory task (N-Back, comprising 3- and 0-back), and task-related blood-oxygen-level-dependent (BOLD) activity was measured in the last session with functional magnetic resonance imaging. Compared to placebo, participants showed a higher error rate and a longer reaction time in 3- against 0-back trials in the caffeine condition; also, in the withdrawal condition we observed a higher error rate compared to placebo. However, task-related BOLD activity, i.e., an increased attention network and decreased default mode network activity in 3- versus 0-back, did not show significant differences among three conditions. Interestingly, irrespective of 3- or 0-back, BOLD activity was reduced in the right hippocampus in the caffeine condition compared to placebo. Adding to the earlier evidence showing increasing cerebral metabolic demands for WM function after acute caffeine intake, our data suggest that such demands might be impeded over daily intake and therefore result in a worse performance. Finally, the reduced hippocampal activity may reflect caffeine-associated hippocampal grey matter plasticity reported in the previous analysis. The findings of this study reveal an adapted neurocognitive response to daily caffeine exposure and highlight the importance of classifying impacts of caffeine on clinical and healthy populations.
急性摄入咖啡因已被发现可增加健康成年人与工作记忆(WM)相关的大脑活动,而不会改善行为表现。然而,目前尚不清楚每日咖啡因摄入(这是全球 80%的人共同的习惯)及其停止对工作记忆及其神经相关因素的影响。在这项双盲、随机、交叉研究中,我们在 10 天的咖啡因(150mg×3 次/天)、10 天的安慰剂(3 次/天)和戒断期(9 天的咖啡因后 1 天的安慰剂)中,检查了 20 名年轻健康的非吸烟者(年龄:26.4±4.0 岁;体重指数:22.7±1.4kg/m;习惯性咖啡因摄入量:474.1±107.5mg/天)的工作记忆功能。在每个条件的第 10 天,参与者进行了四次工作记忆任务(N-Back,包括 3-和 0-背),并在最后一次使用功能磁共振成像测量与任务相关的血氧水平依赖(BOLD)活性。与安慰剂相比,参与者在咖啡因条件下的 3-对 0-背试验中表现出更高的错误率和更长的反应时间;此外,在戒断期,我们观察到与安慰剂相比错误率更高。然而,与任务相关的 BOLD 活性,即 3-对 0-背时注意力网络的增加和默认模式网络的减少,在三种条件之间没有显示出显著差异。有趣的是,无论 3-还是 0-背,与安慰剂相比,咖啡因条件下右海马的 BOLD 活性降低。除了先前的研究表明急性咖啡因摄入后 WM 功能的大脑代谢需求增加外,我们的数据表明,这种需求可能会因日常摄入而受到阻碍,从而导致表现更差。最后,海马体活性的降低可能反映了之前分析中报告的咖啡因相关的海马灰质可塑性。这项研究的结果揭示了对日常咖啡因暴露的适应性神经认知反应,并强调了对临床和健康人群中咖啡因影响进行分类的重要性。