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Research ArticleNew Research, Cognition and Behavior

Noninvasive Brain Stimulation Enhances Memory Acquisition and Is Associated with Synaptoneurosome Modification in the Rat Hippocampus

Seung Ho Jung, Candice Hatcher-Solis, Raquel Moore, Naomi Bechmann, Sean Harshman, Jennifer Martin and Ryan Jankord
eNeuro 7 November 2019, 6 (6) ENEURO.0311-19.2019; https://doi.org/10.1523/ENEURO.0311-19.2019
Seung Ho Jung
1Applied Neuroscience Branch, 711th Human Performance Wing, Air Force Research Laboratory, Wright-Patterson AFB, OH 45433
2Research Associateship Program, National Research Council, National Academies of Science, Washington, DC 200001
3ORISE, Oak Ridge, TN 37830
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Candice Hatcher-Solis
1Applied Neuroscience Branch, 711th Human Performance Wing, Air Force Research Laboratory, Wright-Patterson AFB, OH 45433
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  • ORCID record for Candice Hatcher-Solis
Raquel Moore
1Applied Neuroscience Branch, 711th Human Performance Wing, Air Force Research Laboratory, Wright-Patterson AFB, OH 45433
4Infoscitex, Dayton, OH 45431
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Naomi Bechmann
1Applied Neuroscience Branch, 711th Human Performance Wing, Air Force Research Laboratory, Wright-Patterson AFB, OH 45433
4Infoscitex, Dayton, OH 45431
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Sean Harshman
5UES, Inc, Dayton, OH 45432
6Human Signatures Branch, 711th Human Performance Wing, Air Force Research Laboratory, Wright-Patterson AFB, OH 45433
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Jennifer Martin
6Human Signatures Branch, 711th Human Performance Wing, Air Force Research Laboratory, Wright-Patterson AFB, OH 45433
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Ryan Jankord
1Applied Neuroscience Branch, 711th Human Performance Wing, Air Force Research Laboratory, Wright-Patterson AFB, OH 45433
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Abstract

Transcranial direct-current stimulation (tDCS) is a non-invasive brain stimulation approach previously shown to enhance memory acquisition, but more studies are needed to elucidate the underlying mechanisms. Here, we examined the effects of anodal tDCS (0.25 mA for 30 min) on the memory performance of male Sprague Dawley rats in the passive avoidance test (PAT) and the associated modifications to the hippocampal proteomes. Results indicate anodal tDCS applied before the acquisition period significantly enhanced memory performance in the PAT. Following PAT, synaptoneurosomes were biochemically purified from the hippocampi of tDCS-treated or sham-treated rats and individual protein abundances were determined by bottom-up liquid chromatography mass spectrometry analysis. Proteomic analysis identified 184 differentially expressed hippocampal proteins when comparing the sham to the tDCS before memory acquisition treatment group. Ingenuity pathway analysis (IPA) showed anodal tDCS before memory acquisition significantly enhanced pathways associated with memory, cognition, learning, transmission, neuritogenesis, and long-term potentiation (LTP). IPA identified significant upstream regulators including bdnf, shank3, and gsk3b. Protein-protein interaction (PPI) and protein sequence similarity (PSS) networks show that glutamate receptor pathways, ion channel activity, memory, learning, cognition, and long-term memory were significantly associated with anodal tDCS. Centrality measures from both networks identified key proteins including dlg, shank, grin, and gria that were significantly modified by tDCS applied before the acquisition period. Together, our results provide descriptive molecular evidence that anodal tDCS enhances memory performance in the PAT by modifying hippocampal synaptic plasticity related proteins.

  • hippocampal proteomics
  • hippocampal synaptoneurosome
  • memory process
  • protein sequence similarity network
  • protein-protein interaction network
  • transcranial direct current stimulation

Footnotes

  • The authors declare no competing financial interests.

  • This work was supported by Air Force Office of Scientific Research Grants 13RH14COR and 16RHCOR362 and has been approved for public release (Distribution A: Approved for public release, 88ABW Cleared July 5, 2019; 88ABW-2019-3239).

This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

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eneuro: 6 (6)
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November/December 2019
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Noninvasive Brain Stimulation Enhances Memory Acquisition and Is Associated with Synaptoneurosome Modification in the Rat Hippocampus
Seung Ho Jung, Candice Hatcher-Solis, Raquel Moore, Naomi Bechmann, Sean Harshman, Jennifer Martin, Ryan Jankord
eNeuro 7 November 2019, 6 (6) ENEURO.0311-19.2019; DOI: 10.1523/ENEURO.0311-19.2019

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Noninvasive Brain Stimulation Enhances Memory Acquisition and Is Associated with Synaptoneurosome Modification in the Rat Hippocampus
Seung Ho Jung, Candice Hatcher-Solis, Raquel Moore, Naomi Bechmann, Sean Harshman, Jennifer Martin, Ryan Jankord
eNeuro 7 November 2019, 6 (6) ENEURO.0311-19.2019; DOI: 10.1523/ENEURO.0311-19.2019
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Keywords

  • hippocampal proteomics
  • hippocampal synaptoneurosome
  • memory process
  • protein sequence similarity network
  • protein-protein interaction network
  • transcranial direct current stimulation

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