Emotion Neuroimaging Lab, Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.
International Max Planck Research School NeuroCom, Leipzig, Germany.
Hum Brain Mapp. 2022 Apr 15;43(6):1868-1881. doi: 10.1002/hbm.25760. Epub 2022 Jan 22.
Neural health relies on cortical excitation-inhibition balance (EIB). Previous research suggests a link between increased cortical excitation and neuroplasticity induced by selective serotonin reuptake inhibitors (SSRIs). Whether there are modulations of EIB following SSRI-administration in the healthy human brain, however, remains unclear. Thus, in a randomized double-blind study, we administered a clinically relevant dose of 20 mg escitalopram for 7 days (time when steady state is achieved) in 59 healthy women (28 escitalopram, 31 placebo) on oral contraceptives. We acquired resting-state electroencephalography data at baseline, after a single dose, and at steady state. We assessed 1/f slope of the power spectrum as a marker of EIB, compared individual trajectories of 1/f slope changes contrasting single dose and 1-week drug intake, and tested the relationship of escitalopram plasma levels and cortical excitatory and inhibitory balance shifts. Escitalopram-intake was associated with decreased 1/f slope, indicating an EIB shift in favor of excitation. Furthermore, 1/f slope at baseline and after a single dose of escitalopram was associated with 1/f slope at steady state. Higher plasma escitalopram levels at a single dose were associated with better maintenance of these EIB changes throughout the drug administration week. These findings demonstrate the potential for 1/f slope to predict individual cortical responsivity to SSRIs and widen the lens through which we map the human brain by testing an interventional psychopharmacological design in a clearly defined endocrinological state.
神经健康依赖于皮层兴奋抑制平衡(EIB)。先前的研究表明,皮质兴奋增加与选择性 5-羟色胺再摄取抑制剂(SSRIs)诱导的神经可塑性之间存在关联。然而,在健康人的大脑中,SSRIs 给药后是否存在 EIB 的调节仍不清楚。因此,在一项随机双盲研究中,我们在口服避孕药的 59 名健康女性(28 名接受艾司西酞普兰,31 名接受安慰剂)中,以临床相关剂量 20mg 艾司西酞普兰给药 7 天(达到稳态时)。我们在基线、单次剂量后和稳态时采集静息状态脑电图数据。我们评估了功率谱的 1/f 斜率作为 EIB 的标志物,比较了单剂量和 1 周药物摄入的 1/f 斜率变化的个体轨迹,并测试了艾司西酞普兰血浆水平与皮质兴奋性和抑制性平衡变化的关系。艾司西酞普兰摄入与 1/f 斜率降低有关,表明 EIB 向兴奋倾斜。此外,基线和单次艾司西酞普兰剂量后的 1/f 斜率与稳态时的 1/f 斜率相关。单次剂量时更高的艾司西酞普兰血浆水平与整个药物治疗周内更好地维持这些 EIB 变化相关。这些发现表明,1/f 斜率有可能预测个体对 SSRIs 的皮质反应性,并通过在明确的内分泌状态下测试干预性精神药理学设计,拓宽我们对人类大脑进行映射的视角。