Modulation of Long-Term Potentiation by Gamma Frequency Transcranial Alternating Current Stimulation in Transgenic Mouse Models of Alzheimer’s Disease

Transcranial alternating current stimulation (tACS) is a neuromodulation procedure that is currently studied for the purpose of improving cognitive function in various diseases. A few studies have shown positive effects of tACS in Alzheimer’s disease (AD). However, the mechanism underlying tACS has...

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Autores principales: Won-Hyeong Jeong, Wang-In Kim, Jin-Won Lee, Hyeng-Kyu Park, Min-Keun Song, In-Sung Choi, Jae-Young Han
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:5107fa790bf54296ab879efaaa5d88cf2021-11-25T16:59:13ZModulation of Long-Term Potentiation by Gamma Frequency Transcranial Alternating Current Stimulation in Transgenic Mouse Models of Alzheimer’s Disease10.3390/brainsci111115322076-3425https://doaj.org/article/5107fa790bf54296ab879efaaa5d88cf2021-11-01T00:00:00Zhttps://www.mdpi.com/2076-3425/11/11/1532https://doaj.org/toc/2076-3425Transcranial alternating current stimulation (tACS) is a neuromodulation procedure that is currently studied for the purpose of improving cognitive function in various diseases. A few studies have shown positive effects of tACS in Alzheimer’s disease (AD). However, the mechanism underlying tACS has not been established. The purpose of this study was to investigate the mechanism of tACS in five familial AD mutation (5xFAD) mouse models. We prepared twenty 4-month-old mice and divided them into four groups: wild-type mice without stimulation (WT-NT group), wild-type mice with tACS (WT-T group), 5xFAD mice without stimulation (AD-NT group), and 5xFAD mice with tACS (AD-T group). The protocol implemented was as follows: gamma frequency 200 μA over the bilateral frontal lobe for 20 min over 2 weeks. The following tests were conducted: excitatory postsynaptic potential (EPSP) recording, Western blot analysis (cyclic AMP response element-binding (CREB) proteins, phosphorylated CREB proteins, brain-derived neurotrophic factor, and parvalbumin) to examine the synaptic plasticity. The EPSP was remarkably increased in the AD-T group compared with in the AD-NT group. In the Western blot analysis, the differences among the groups were not significant. Hence, tACS can affect the long-lasting enhancement of synaptic transmission in mice models of AD.Won-Hyeong JeongWang-In KimJin-Won LeeHyeng-Kyu ParkMin-Keun SongIn-Sung ChoiJae-Young HanMDPI AGarticletranscranial alternating current stimulationAlzheimer’s diseasenoninvasive brain stimulationgamma frequencylong-term potentiationsynaptic plasticityNeurosciences. Biological psychiatry. NeuropsychiatryRC321-571ENBrain Sciences, Vol 11, Iss 1532, p 1532 (2021)
institution DOAJ
collection DOAJ
language EN
topic transcranial alternating current stimulation
Alzheimer’s disease
noninvasive brain stimulation
gamma frequency
long-term potentiation
synaptic plasticity
Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
spellingShingle transcranial alternating current stimulation
Alzheimer’s disease
noninvasive brain stimulation
gamma frequency
long-term potentiation
synaptic plasticity
Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Won-Hyeong Jeong
Wang-In Kim
Jin-Won Lee
Hyeng-Kyu Park
Min-Keun Song
In-Sung Choi
Jae-Young Han
Modulation of Long-Term Potentiation by Gamma Frequency Transcranial Alternating Current Stimulation in Transgenic Mouse Models of Alzheimer’s Disease
description Transcranial alternating current stimulation (tACS) is a neuromodulation procedure that is currently studied for the purpose of improving cognitive function in various diseases. A few studies have shown positive effects of tACS in Alzheimer’s disease (AD). However, the mechanism underlying tACS has not been established. The purpose of this study was to investigate the mechanism of tACS in five familial AD mutation (5xFAD) mouse models. We prepared twenty 4-month-old mice and divided them into four groups: wild-type mice without stimulation (WT-NT group), wild-type mice with tACS (WT-T group), 5xFAD mice without stimulation (AD-NT group), and 5xFAD mice with tACS (AD-T group). The protocol implemented was as follows: gamma frequency 200 μA over the bilateral frontal lobe for 20 min over 2 weeks. The following tests were conducted: excitatory postsynaptic potential (EPSP) recording, Western blot analysis (cyclic AMP response element-binding (CREB) proteins, phosphorylated CREB proteins, brain-derived neurotrophic factor, and parvalbumin) to examine the synaptic plasticity. The EPSP was remarkably increased in the AD-T group compared with in the AD-NT group. In the Western blot analysis, the differences among the groups were not significant. Hence, tACS can affect the long-lasting enhancement of synaptic transmission in mice models of AD.
format article
author Won-Hyeong Jeong
Wang-In Kim
Jin-Won Lee
Hyeng-Kyu Park
Min-Keun Song
In-Sung Choi
Jae-Young Han
author_facet Won-Hyeong Jeong
Wang-In Kim
Jin-Won Lee
Hyeng-Kyu Park
Min-Keun Song
In-Sung Choi
Jae-Young Han
author_sort Won-Hyeong Jeong
title Modulation of Long-Term Potentiation by Gamma Frequency Transcranial Alternating Current Stimulation in Transgenic Mouse Models of Alzheimer’s Disease
title_short Modulation of Long-Term Potentiation by Gamma Frequency Transcranial Alternating Current Stimulation in Transgenic Mouse Models of Alzheimer’s Disease
title_full Modulation of Long-Term Potentiation by Gamma Frequency Transcranial Alternating Current Stimulation in Transgenic Mouse Models of Alzheimer’s Disease
title_fullStr Modulation of Long-Term Potentiation by Gamma Frequency Transcranial Alternating Current Stimulation in Transgenic Mouse Models of Alzheimer’s Disease
title_full_unstemmed Modulation of Long-Term Potentiation by Gamma Frequency Transcranial Alternating Current Stimulation in Transgenic Mouse Models of Alzheimer’s Disease
title_sort modulation of long-term potentiation by gamma frequency transcranial alternating current stimulation in transgenic mouse models of alzheimer’s disease
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/5107fa790bf54296ab879efaaa5d88cf
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