Sahlem Gregory L, Badran Bashar W, Halford Jonathan J, Williams Nolan R, Korte Jeffrey E, Leslie Kimberly, Strachan Martha, Breedlove Jesse L, Runion Jennifer, Bachman David L, Uhde Thomas W, Borckardt Jeffery J, George Mark S
Department of Psychiatry, Medical University of South Carolina, 67 President St., 502N, Charleston, SC 29425, USA.
Department of Psychiatry, Medical University of South Carolina, 67 President St., 502N, Charleston, SC 29425, USA; Department of Neurosciences, Medical University of South Carolina, 68 President St, BE 101, MSC 501, Charleston, SC 29425, USA.
Brain Stimul. 2015 May-Jun;8(3):528-34. doi: 10.1016/j.brs.2015.01.414. Epub 2015 Feb 16.
A 2006 trial in healthy medical students found that anodal slow oscillating tDCS delivered bi-frontally during slow wave sleep had an enhancing effect in declarative, but not procedural memory. Although there have been supporting animal studies, and similar findings in pathological groups, this study has not been replicated, or refuted, in the intervening years. We therefore tested these earlier results for replication using similar methods with the exception of current waveform (square in our study, nearly sinusoidal in the original).
OBJECTIVE/HYPOTHESIS: Our objective was to test the findings of a 2006 trial suggesting bi-frontal anodal tDCS during slow wave sleep enhances declarative memory.
Twelve students (mean age 25, 9 women) free of medical problems underwent two testing conditions (active, sham) in a randomized counterbalanced fashion. Active stimulation consisted of oscillating square wave tDCS delivered during early Non-Rapid Eye Movement (NREM) sleep. The sham condition consisted of setting-up the tDCS device and electrodes, but not turning it on during sleep. tDCS was delivered bi-frontally with anodes placed at F3/F4, and cathodes placed at mastoids. Current density was 0.517 mA/cm(2), and oscillated between zero and maximal current at a frequency of 0.75 Hz. Stimulation occurred during five-five minute blocks with 1-min inter-block intervals (25 min total stimulation). The primary outcomes were both declarative memory consolidation measured by a paired word association test (PWA), and non-declarative memory, measured by a non-dominant finger-tapping test (FTT). We also recorded and analyzed sleep EEG.
There was no difference in the number of paired word associations remembered before compared to after sleep [(active = 3.1 ± 3.0 SD more associations) (sham = 3.8 ± 3.1 SD more associations)]. Finger tapping improved, (non-significantly) following active stimulation [(3.6 ± 2.7 SD correctly typed sequences) compared to sham stimulation (2.3 ± 2.2 SD correctly typed sequences)].
In this study, we failed to find improvements in declarative or performance memory and could not replicate an earlier study using nearly identical settings. Specifically we failed to find a beneficial effect on either overnight declarative or non-declarative memory consolidation via square-wave oscillating tDCS intervention applied bi-frontally during early NREM sleep. It is unclear if the morphology of the tDCS pulse is critical in any memory related improvements.
2006年一项针对健康医学生的试验发现,在慢波睡眠期间双侧额叶给予阳极慢振荡经颅直流电刺激(tDCS)对陈述性记忆有增强作用,但对程序性记忆无增强作用。尽管有支持性的动物研究以及在病理群体中的类似发现,但在随后的几年里,这项研究既未被重复验证,也未被反驳。因此,我们采用类似方法(除电流波形外,我们的研究中为方波,原研究中接近正弦波)对这些早期结果进行重复验证。
目的/假设:我们的目的是验证2006年一项试验的结果,该试验表明在慢波睡眠期间双侧额叶阳极tDCS可增强陈述性记忆。
12名无医学问题的学生(平均年龄25岁,9名女性)以随机平衡的方式接受两种测试条件(主动、假刺激)。主动刺激包括在早期非快速眼动(NREM)睡眠期间给予振荡方波tDCS。假刺激条件包括设置tDCS设备和电极,但在睡眠期间不开启。tDCS双侧额叶给予,阳极置于F3/F4,阴极置于乳突。电流密度为0.517 mA/cm²,以0.75 Hz的频率在零和最大电流之间振荡。刺激在五个五分钟的时间段内进行,每个时间段之间有1分钟的间隔(总刺激时间25分钟)。主要结果包括通过配对词联想测试(PWA)测量的陈述性记忆巩固,以及通过非优势手指敲击测试(FTT)测量的非陈述性记忆。我们还记录并分析了睡眠脑电图。
睡眠前后记住的配对词联想数量没有差异[(主动组 = 多3.1 ± 3.0个标准差的联想)(假刺激组 = 多3.8 ± 3.1个标准差的联想)]。与假刺激相比,主动刺激后手指敲击有改善(不显著)[(正确敲击序列3.6 ± 2.7个标准差)与假刺激(正确敲击序列2.3 ± 2.2个标准差)相比]。
在本研究中,我们未发现陈述性或操作记忆有改善,且未能重复一项使用几乎相同设置的早期研究。具体而言,我们未发现通过在早期NREM睡眠期间双侧额叶应用方波振荡tDCS干预对夜间陈述性或非陈述性记忆巩固有有益影响。尚不清楚tDCS脉冲的形态在任何与记忆相关的改善中是否至关重要。