Skip to main content

GENERAL COMMENTARY article

Front. Psychol., 30 May 2017
Sec. Cognition

Commentary: Stimulation of the Posterior Cortical-Hippocampal Network Enhances Precision of Memory Recollection

  • 1School of Psychology, Nanjing Normal University, Nanjing, China
  • 2School of Education Science, Nanjing Normal University, Nanjing, China
  • 3Faculty of Education, University of Hong Kong, Hong Kong, Hong Kong
  • 4School of Mental Health, Wenzhou Medical University, Wenzhou, China

A commentary on
Stimulation of the Posterior Cortical-Hippocampal Network Enhances Precision of Memory Recollection

by Nilakantan, A. S., Bridge, D. J., Gagnon, E. P., Vanhaerents, S. A., and Voss, J. L. (2017). Curr. Biol. 27, 465–470. doi: 10.1016/j.cub.2016.12.042

Memory is critical to our daily life. Various strategies have been employed to promote cognitive performance, such as pharmacological tools, physical exercise, and cognitive training (Stern and Alberini, 2013; Kelly, 2015). In recent years, non-invasive neuromodulation techniques [e.g., transcranial magnetic stimulation (TMS) and transcranial direct current stimulation (tDCS); Sparing and Mottaghy, 2008; Hansen, 2014; Rose et al., 2016; Voarino et al., 2016] are demonstrating prospective future in memory retrieval and enhancement.

Episodic memory refers to the memory of specific events taken place in the past, which relies on the interactions between hippocampus and other brain regions (Ranganath and Ritchey, 2012). Among various brain regions that mediate different functions, the hippocampal posterior-medial (HPM) network is specifically associated with the recall of highly precise contextual and spatial information (Nadel et al., 2013). In a previous study, Rose et al. demonstrated that TMS was effective for improving memory performance (Rose et al., 2016). Another study utilized TMS to stimulate the HPM network and found that TMS could improve the recollection of paired-associate cued items and increase functional connectivity within the HPM network (Wang et al., 2014). However, it was still unknown if this intervention would improve memory precision.

The recent study published in Current Biology by Nilakantan et al. explored for the first time the causal role of the HPM network in recollection precision (Nilakantan et al., 2017). Recollection precision refers to the memories that require the recall on details of the targeted objects, which is distinguished from general recollection in memory tasks. In this study, the authors employed an object-location memory task and participants were asked to memorize the object-locations as accurately as possible. Based on high functional connectivity between the lateral-parietal cortex and hippocampus (Kahn et al., 2008), the researchers chose the lateral-parietal cortex as the stimulation site to target HPM network as previous study (Wang et al., 2014). On the second day, participants were asked to perform the task, followed by 5-days' continuous repetitive TMS (rTMS) and another object-locations task with electroencephalogram/event-related potentials (EEG/ERP) recorded. The results demonstrated that HPM targeting TMS stimulation could reduce the ERP responses to recollection, associated with significant improve in recalling precision.

Nilakantan et al. used TMS to change episodic memory precision and extended previous lesion-based studies for human brain network involvement in memory. Besides, TMS can be also applied to modulate other forms of memory. A study showed that rhythmic TMS could enhance auditory working memory performance (Albouy et al., 2017). Rademaker et al. also proved that a visual working memory precision-enhancing effect could be found at visual cortex (Rademaker et al., 2017). Therefore, TMS may have great potential value in human memory system in the future.

With the power of image-guided TMS, researchers can activate a specific circuit and explore its effect in human brain. Previous studies have explored the effect of TMS on human cognition (Luber and Lisanby, 2014). TMS was adopted to activate latent working memory with a relatively short temporal efficiency (Rose et al., 2016). In present study, 5-days' continuous TMS treatment enhance memory for at least 24 hours. It can be implied from the study that continuous rTMS is considerably more effective for enhancing memories than short and sporadic stimulations.

There were still some limitations of the present study. First, the mechanisms underlying the TMS-induced enhancement of HPM network activity are unclear. Future studies are required to confirm the importance of structure modification or functional changes in these neural circuits. Furthermore, most TMS coils only target the cortical layers in the brain and activate subcortical structures indirectly. In the future, it may be possible to develop deep brain stimulation-inspired TMS stimulation with more focused TMS coils or deep TMS coils. Last but not least, the stimulation parameters could be optimized to further enhance memory.

In the future, it will be interesting to understand if interventions in the HPM network could as well reduce certain memory precisely, and erase unwanted memory as the case for post-traumatic stress disorder (PTSD). In fact, pairing stimulation could result in bi-directional plasticity with varied temporal interval (Koch et al., 2013), and such approach would allow for the “un-learning” of “dark memories,” including fear and addiction.

Author Contributions

All authors designed the study, wrote the manuscript together, and approved the final version of the manuscript. TL and MF contributed equally to this work.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

The authors thank their department for support.

References

Albouy, P., Weiss, A., Baillet, S., and Zatorre, R. J. (2017). Selective entrainment of theta oscillations in the dorsal stream causally enhances auditory working memory performance. Neuron 94, 193. doi: 10.1016/j.neuron.2017.03.015

PubMed Abstract | CrossRef Full Text | Google Scholar

Hansen, N. (2014). Brain stimulation for combating Alzheimer's disease. Front. Neurol. 5:80. doi: 10.3389/fneur.2014.00080

PubMed Abstract | CrossRef Full Text | Google Scholar

Kahn, I., Andrews-Hanna, J. R., Vincent, J. L., Snyder, A. Z., and Buckner, R. L. (2008). Distinct cortical anatomy linked to subregions of the medial temporal lobe revealed by intrinsic functional connectivity. J. Neurophysiol. 100, 129–139. doi: 10.1152/jn.00077.2008

PubMed Abstract | CrossRef Full Text | Google Scholar

Kelly, A. M. (2015). Non-pharmacological approaches to cognitive enhancement. Handb. Exp. Pharmacol. 228, 417–439. doi: 10.1007/978-3-319-16522-6_14

PubMed Abstract | CrossRef Full Text | Google Scholar

Koch, G., Ponzo, V., Di Lorenzo, F., Caltagirone, C., and Veniero, D. (2013). Hebbian and anti-Hebbian spike-timing-dependent plasticity of human cortico-cortical connections. J. Neurosci. 33, 9725–9733. doi: 10.1523/JNEUROSCI.4988-12.2013

PubMed Abstract | CrossRef Full Text | Google Scholar

Luber, B., and Lisanby, S. H. (2014). Enhancement of human cognitive performance using transcranial magnetic stimulation (TMS). Neuroimage 85(Pt 3), 961–970. doi: 10.1016/j.neuroimage.2013.06.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Nadel, L., Hoscheidt, S., and Ryan, L. R. (2013). Spatial cognition and the hippocampus: the anterior-posterior axis. J. Cogn. Neurosci. 25, 22–28. doi: 10.1162/jocn_a_00313

PubMed Abstract | CrossRef Full Text | Google Scholar

Nilakantan, A. S., Bridge, D. J., Gagnon, E. P., Vanhaerents, S. A., and Voss, J. L. (2017). Stimulation of the posterior cortical-hippocampal network enhances precision of memory recollection. Curr. Biol. 27, 465–470. doi: 10.1016/j.cub.2016.12.042

PubMed Abstract | CrossRef Full Text | Google Scholar

Rademaker, R. L., Van De Ven, V. G., Tong, F., and Sack, A. T. (2017). The impact of early visual cortex transcranial magnetic stimulation on visual working memory precision and guess rate. PLoS ONE 12:e0175230. doi: 10.1371/journal.pone.0175230

PubMed Abstract | CrossRef Full Text | Google Scholar

Ranganath, C., and Ritchey, M. (2012). Two cortical systems for memory-guided behaviour. Nat. Rev. Neurosci. 13, 713–726. doi: 10.1038/nrn3338

PubMed Abstract | CrossRef Full Text | Google Scholar

Rose, N. S., Larocque, J. J., Riggall, A. C., Gosseries, O., Starrett, M. J., Meyering, E. E., et al. (2016). Reactivation of latent working memories with transcranial magnetic stimulation. Science 354, 1136. doi: 10.1126/science.aah7011

PubMed Abstract | CrossRef Full Text | Google Scholar

Sparing, R., and Mottaghy, F. M. (2008). Noninvasive brain stimulation with transcranial magnetic or direct current stimulation (TMS/tDCS)-from insights into human memory to therapy of its dysfunction. Methods 44, 329–337. doi: 10.1016/j.ymeth.2007.02.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Stern, S. A., and Alberini, C. M. (2013). Mechanisms of memory enhancement. Wiley Interdiscip. Rev. Syst. Biol. Med. 5, 37–53. doi: 10.1002/wsbm.1196

PubMed Abstract | CrossRef Full Text | Google Scholar

Voarino, N., Dubljevic, V., and Racine, E. (2016). tDCS for memory enhancement: analysis of the speculative aspects of ethical issues. Front. Hum. Neurosci. 10:678. doi: 10.3389/fnhum.2016.00678

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, J. X., Rogers, L. M., Gross, E. Z., Ryals, A. J., Dokucu, M. E., Brandstatt, K. L., et al. (2014). Targeted enhancement of cortical-hippocampal brain networks and associative memory. Science 345, 1054–1057. doi: 10.1126/science.1252900

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: memory, TMS, cognition, memory enhancement, tDCS

Citation: Liu T, Fu M, Yuan T and Xu D-W (2017) Commentary: Stimulation of the Posterior Cortical-Hippocampal Network Enhances Precision of Memory Recollection. Front. Psychol. 8:899. doi: 10.3389/fpsyg.2017.00899

Received: 05 April 2017; Accepted: 16 May 2017;
Published: 30 May 2017.

Edited by:

Claudia Repetto, Università Cattolica del Sacro Cuore, Italy

Reviewed by:

Brandi Ormerod, University of Florida, United States
Anna Fertonani, Centro San Giovanni di Dio Fatebenefratelli (IRCCS), Italy

Copyright © 2017 Liu, Fu, Yuan and Xu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Tifei Yuan, ytf0707@126.com
Dong-Wu Xu, wzxdw@126.com

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.