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Electroacupuncture Mitigates Hippocampal Cognitive Impairments by Reducing BACE1 Deposition and Activating PKA in APP/PS1 Double Transgenic Mice
Increased amyloid-β (Aβ) plaque deposition is thought to be the main cause of Alzheimer’s disease (AD). β-Site amyloid precursor protein cleaving enzyme 1 (BACE1) is the key protein involved in Aβ peptide generation. Excessive expression of BACE1 might cause overproduction of neurotoxins in the cent...
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Published in: | Journal of neural transplantation & plasticity 2019-01, Vol.2019 (2019), p.1-12 |
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container_title | Journal of neural transplantation & plasticity |
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creator | Xiang, Dulian Li, Zhigang Xu, Anping Cao, Jin Zhou, You Guo, Yu Shao, Shujun Tang, Yinshan Wu, Jihong |
description | Increased amyloid-β (Aβ) plaque deposition is thought to be the main cause of Alzheimer’s disease (AD). β-Site amyloid precursor protein cleaving enzyme 1 (BACE1) is the key protein involved in Aβ peptide generation. Excessive expression of BACE1 might cause overproduction of neurotoxins in the central nervous system. Previous studies indicated that BACE1 initially cleaves the amyloid precursor protein (APP) and may subsequently interfere with physiological functions of proteins such as PKA, which is recognized to be closely associated with long-term potentiation (LTP) level and can effectively ameliorate cognitive impairments. Therefore, revealing the underlying mechanism of BACE1 in the pathogenesis of AD might have a significant impact on the future development of therapeutic agents targeting dementia. This study examined the effects of electroacupuncture (EA) stimulation on BACE1, APP, and p-PKA protein levels in hippocampal tissue samples. Memory and learning abilities were assessed using the Morris water maze test after EA intervention. Immunofluorescence, immunohistochemistry, and western blot were employed to assess the distribution patterns and expression levels of BACE1, APP, and p-PKA, respectively. The results showed the downregulation of BACE1 and APP and the activation of PKA by EA. In summary, EA treatment might reduce BACE1 deposition in APP/PS1 transgenic mice and regulate PKA and its associated substrates, such as LTP to change memory and learning abilities. |
doi_str_mv | 10.1155/2019/2823679 |
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Excessive expression of BACE1 might cause overproduction of neurotoxins in the central nervous system. Previous studies indicated that BACE1 initially cleaves the amyloid precursor protein (APP) and may subsequently interfere with physiological functions of proteins such as PKA, which is recognized to be closely associated with long-term potentiation (LTP) level and can effectively ameliorate cognitive impairments. Therefore, revealing the underlying mechanism of BACE1 in the pathogenesis of AD might have a significant impact on the future development of therapeutic agents targeting dementia. This study examined the effects of electroacupuncture (EA) stimulation on BACE1, APP, and p-PKA protein levels in hippocampal tissue samples. Memory and learning abilities were assessed using the Morris water maze test after EA intervention. Immunofluorescence, immunohistochemistry, and western blot were employed to assess the distribution patterns and expression levels of BACE1, APP, and p-PKA, respectively. The results showed the downregulation of BACE1 and APP and the activation of PKA by EA. In summary, EA treatment might reduce BACE1 deposition in APP/PS1 transgenic mice and regulate PKA and its associated substrates, such as LTP to change memory and learning abilities.</description><identifier>ISSN: 2090-5904</identifier><identifier>ISSN: 0792-8483</identifier><identifier>EISSN: 1687-5443</identifier><identifier>DOI: 10.1155/2019/2823679</identifier><identifier>PMID: 31223308</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Acupuncture ; Advertising executives ; Alzheimer's disease ; Amyloid beta-protein ; Amyloid beta-Protein Precursor - genetics ; Amyloid Precursor Protein Secretases - metabolism ; Animals ; Antibodies ; Aspartic Acid Endopeptidases - metabolism ; Brain ; Cognitive Dysfunction - metabolism ; Cognitive Dysfunction - therapy ; Cyclic AMP-Dependent Protein Kinases - metabolism ; Dementia ; Disease Models, Animal ; Electroacupuncture ; Enzymes ; Genetic engineering ; Hippocampus - metabolism ; Immunohistochemistry ; Kinases ; Male ; Maze Learning - physiology ; Memory ; Mice ; Mice, Transgenic ; Neurodegeneration ; Older people ; Peptides ; Phosphorylation ; Physiological aspects ; Presenilin-1 - genetics ; Proteins ; Transgenic animals</subject><ispartof>Journal of neural transplantation & plasticity, 2019-01, Vol.2019 (2019), p.1-12</ispartof><rights>Copyright © 2019 Yinshan Tang et al.</rights><rights>COPYRIGHT 2019 John Wiley & Sons, Inc.</rights><rights>Copyright © 2019 Yinshan Tang et al. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2019 Yinshan Tang et al. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c635t-a6047ea871b726c88d87152ccfe37aa03e0b2d3e3553039a8a1b8a716690d3fe3</citedby><cites>FETCH-LOGICAL-c635t-a6047ea871b726c88d87152ccfe37aa03e0b2d3e3553039a8a1b8a716690d3fe3</cites><orcidid>0000-0001-5692-3689 ; 0000-0002-8798-4430 ; 0000-0003-0378-3496 ; 0000-0002-6822-601X ; 0000-0002-1752-1254</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2407661009/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2407661009?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25730,27900,27901,36988,36989,44565,53765,53767,75095</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31223308$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Wu, Long-Jun</contributor><creatorcontrib>Xiang, Dulian</creatorcontrib><creatorcontrib>Li, Zhigang</creatorcontrib><creatorcontrib>Xu, Anping</creatorcontrib><creatorcontrib>Cao, Jin</creatorcontrib><creatorcontrib>Zhou, You</creatorcontrib><creatorcontrib>Guo, Yu</creatorcontrib><creatorcontrib>Shao, Shujun</creatorcontrib><creatorcontrib>Tang, Yinshan</creatorcontrib><creatorcontrib>Wu, Jihong</creatorcontrib><title>Electroacupuncture Mitigates Hippocampal Cognitive Impairments by Reducing BACE1 Deposition and Activating PKA in APP/PS1 Double Transgenic Mice</title><title>Journal of neural transplantation & plasticity</title><addtitle>Neural Plast</addtitle><description>Increased amyloid-β (Aβ) plaque deposition is thought to be the main cause of Alzheimer’s disease (AD). β-Site amyloid precursor protein cleaving enzyme 1 (BACE1) is the key protein involved in Aβ peptide generation. Excessive expression of BACE1 might cause overproduction of neurotoxins in the central nervous system. Previous studies indicated that BACE1 initially cleaves the amyloid precursor protein (APP) and may subsequently interfere with physiological functions of proteins such as PKA, which is recognized to be closely associated with long-term potentiation (LTP) level and can effectively ameliorate cognitive impairments. Therefore, revealing the underlying mechanism of BACE1 in the pathogenesis of AD might have a significant impact on the future development of therapeutic agents targeting dementia. This study examined the effects of electroacupuncture (EA) stimulation on BACE1, APP, and p-PKA protein levels in hippocampal tissue samples. Memory and learning abilities were assessed using the Morris water maze test after EA intervention. Immunofluorescence, immunohistochemistry, and western blot were employed to assess the distribution patterns and expression levels of BACE1, APP, and p-PKA, respectively. The results showed the downregulation of BACE1 and APP and the activation of PKA by EA. 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physiology</subject><subject>Memory</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Neurodegeneration</subject><subject>Older people</subject><subject>Peptides</subject><subject>Phosphorylation</subject><subject>Physiological aspects</subject><subject>Presenilin-1 - genetics</subject><subject>Proteins</subject><subject>Transgenic animals</subject><issn>2090-5904</issn><issn>0792-8483</issn><issn>1687-5443</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNksFu1DAQhiMEoqVw44wsISEk2NaOY8e5IC1LoRVFrKCcrYkzybrK2sFOivoWPDJetrRdxAH5YHvmm3_k35NlTxk9ZEyIo5yy6ihXOZdldS_bZ1KVM1EU_H62n9OKzkRFi73sUYwXlBZSCPEw2-Mszzmnaj_7edyjGYMHMw2TM-MUkHyyo-1gxEhO7DB4A-sBerLwnUuJSySn6W7DGt0YSX1FvmAzGes68na-OGbkHQ4-JtA7Aq4hc5NqYNzklx_nxDoyXy6Pll8T6Ke6R3IewMUOnTWpscHH2YMW-ohPrveD7Nv74_PFyezs84fTxfxsZiQX4wwkLUoEVbK6zKVRqklHkRvTIi8BKEda5w1HLgSnvAIFrFZQMikr2vAEHWSnW93Gw4Uegl1DuNIerP4d8KHTEEZretSqbArDq-SmqIoaRNWiKrlSpaHYtMIkrTdbrWGq19iY5EyAfkd0N-PsSnf-UktRsKqgSeDltUDw3yeMo17baLDvwaGfos7zQkimqNqgz_9CL_wUXLJK5wUtpWSUVrdUB-kB1rU-9TUbUT2XjDPOlRSJOvwHlVaDa2u8w9am-E7BizsFK4R-XEXfT5vfjrvg6y1ogo8xYHtjBqN6M7Z6M7b6emwT_uyugTfwnzlNwKstsLKugR_2P-UwMdjCLZ0wWpX8F33__CE</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Xiang, Dulian</creator><creator>Li, Zhigang</creator><creator>Xu, Anping</creator><creator>Cao, Jin</creator><creator>Zhou, You</creator><creator>Guo, Yu</creator><creator>Shao, Shujun</creator><creator>Tang, Yinshan</creator><creator>Wu, Jihong</creator><general>Hindawi Publishing Corporation</general><general>Hindawi</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><general>Wiley</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>M0S</scope><scope>M2M</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PKEHL</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-5692-3689</orcidid><orcidid>https://orcid.org/0000-0002-8798-4430</orcidid><orcidid>https://orcid.org/0000-0003-0378-3496</orcidid><orcidid>https://orcid.org/0000-0002-6822-601X</orcidid><orcidid>https://orcid.org/0000-0002-1752-1254</orcidid></search><sort><creationdate>20190101</creationdate><title>Electroacupuncture Mitigates Hippocampal Cognitive Impairments by Reducing BACE1 Deposition and Activating PKA in APP/PS1 Double Transgenic Mice</title><author>Xiang, Dulian ; Li, Zhigang ; Xu, Anping ; Cao, Jin ; Zhou, You ; Guo, Yu ; Shao, Shujun ; Tang, Yinshan ; Wu, Jihong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c635t-a6047ea871b726c88d87152ccfe37aa03e0b2d3e3553039a8a1b8a716690d3fe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Acupuncture</topic><topic>Advertising executives</topic><topic>Alzheimer's disease</topic><topic>Amyloid beta-protein</topic><topic>Amyloid beta-Protein Precursor - 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Excessive expression of BACE1 might cause overproduction of neurotoxins in the central nervous system. Previous studies indicated that BACE1 initially cleaves the amyloid precursor protein (APP) and may subsequently interfere with physiological functions of proteins such as PKA, which is recognized to be closely associated with long-term potentiation (LTP) level and can effectively ameliorate cognitive impairments. Therefore, revealing the underlying mechanism of BACE1 in the pathogenesis of AD might have a significant impact on the future development of therapeutic agents targeting dementia. This study examined the effects of electroacupuncture (EA) stimulation on BACE1, APP, and p-PKA protein levels in hippocampal tissue samples. Memory and learning abilities were assessed using the Morris water maze test after EA intervention. Immunofluorescence, immunohistochemistry, and western blot were employed to assess the distribution patterns and expression levels of BACE1, APP, and p-PKA, respectively. The results showed the downregulation of BACE1 and APP and the activation of PKA by EA. In summary, EA treatment might reduce BACE1 deposition in APP/PS1 transgenic mice and regulate PKA and its associated substrates, such as LTP to change memory and learning abilities.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>31223308</pmid><doi>10.1155/2019/2823679</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-5692-3689</orcidid><orcidid>https://orcid.org/0000-0002-8798-4430</orcidid><orcidid>https://orcid.org/0000-0003-0378-3496</orcidid><orcidid>https://orcid.org/0000-0002-6822-601X</orcidid><orcidid>https://orcid.org/0000-0002-1752-1254</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acupuncture Advertising executives Alzheimer's disease Amyloid beta-protein Amyloid beta-Protein Precursor - genetics Amyloid Precursor Protein Secretases - metabolism Animals Antibodies Aspartic Acid Endopeptidases - metabolism Brain Cognitive Dysfunction - metabolism Cognitive Dysfunction - therapy Cyclic AMP-Dependent Protein Kinases - metabolism Dementia Disease Models, Animal Electroacupuncture Enzymes Genetic engineering Hippocampus - metabolism Immunohistochemistry Kinases Male Maze Learning - physiology Memory Mice Mice, Transgenic Neurodegeneration Older people Peptides Phosphorylation Physiological aspects Presenilin-1 - genetics Proteins Transgenic animals |
title | Electroacupuncture Mitigates Hippocampal Cognitive Impairments by Reducing BACE1 Deposition and Activating PKA in APP/PS1 Double Transgenic Mice |
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