Cognitive Function of Artemisia argyi H. Fermented by Monascus purpureus under TMT-Induced Learning and Memory Deficits in ICR Mice

The cognitive effect of Artemisia argyi H. under liquid-state fermentation by Monascus purpureus (AAFM), which has cellular antioxidant activity and neuronal cell viability, on trimethyltin- (TMT-) induced learning and memory impairment in Institute of Cancer Research (ICR) mice was confirmed. Tests...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Evidence-based complementary and alternative medicine 2017-01, Vol.2017 (2017), p.1-16
Hauptverfasser: Heo, Ho Jin, Ha, Gi Jeong, Kim, Jong Min, Ha, Jeong Su, Park, Seon Kyeong, Lee, Du Sang, Kang, Jin Yong, Seo, Weon Taek
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 16
container_issue 2017
container_start_page 1
container_title Evidence-based complementary and alternative medicine
container_volume 2017
creator Heo, Ho Jin
Ha, Gi Jeong
Kim, Jong Min
Ha, Jeong Su
Park, Seon Kyeong
Lee, Du Sang
Kang, Jin Yong
Seo, Weon Taek
description The cognitive effect of Artemisia argyi H. under liquid-state fermentation by Monascus purpureus (AAFM), which has cellular antioxidant activity and neuronal cell viability, on trimethyltin- (TMT-) induced learning and memory impairment in Institute of Cancer Research (ICR) mice was confirmed. Tests were conducted to determine the neuroprotective effects against H2O2-induced oxidative stress, and the results showed that AAFM has protective effects through the repression of mitochondrial injury and cellular membrane damage against H2O2-induced neurotoxicity. In animal experiments, such as the Y-maze, passive avoidance, and Morris water maze tests, AAFM also showed excellent ameliorating effects on TMT-induced cognitive dysfunction. After behavioral tests, brain tissues were extracted to assess damage to brain tissue. According to the experimental results, AAFM improved the cholinergic system by upregulating acetylcholine (ACh) contents and inhibiting acetylcholinesterase (AChE) activity. AAFM effectively improved the decline of the superoxide dismutase (SOD) level and the increase of the oxidized glutathione (GSH) ratio and lipid peroxidation (malondialdehyde (MDA) production) caused by TMT-induced oxidative stress. The occurrence of mitochondrial dysfunction and apoptosis was also decreased compared with the TMT group. Finally, quinic acid derivatives were identified as the major phenolic compounds in AAFM using ultra-performance liquid chromatography quadrupole-time-of-flight (UPLC-Q-TOF) MS analysis.
doi_str_mv 10.1155/2017/5809370
format Article
fullrecord <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5610803</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A556064407</galeid><sourcerecordid>A556064407</sourcerecordid><originalsourceid>FETCH-LOGICAL-c499t-c514d8b8fd9c143c313dd4b961f5f39f070837f6c7beda004d5d9a602afd0fab3</originalsourceid><addsrcrecordid>eNqNksGLEzEYxQdR3LV68ywBL4J2N5lJJpOLUKp1Cy2CVPAWMsmXbpaZpCYzKz37j5vS2lVPQiAf5MdLXt4ripcEXxHC2HWJCb9mDRYVx4-KS8IpmdKyaR6fZ_7toniW0h3GpeCcPy0uSoEb0hBxWfych613g7sHtBi9HlzwKFg0iwP0LjmFVNzuHbq5QguIPfgBDGr3aB28SnpMaDfGvCBPozcQ0Wa9mS69GXXmVqCid36LlDdoDX2Ie_QBrNNuSMh5tJx_QWun4XnxxKouwYvTPim-Lj5u5jfT1edPy_lsNdVUiGGqGaGmaRtrhCa00hWpjKGtqIllthIWc9xU3Naat2AUxtQwI1SNS2UNtqqtJsX7o-5ubHswOruJqpO76HoV9zIoJ_8-8e5WbsO9ZDXBDa6ywJuTQAzfR0iDzH-koeuUhzAmSQTjvOY0ZzEpXv-D3oUx-mwvU7QkOaGaPlBb1YF03oZ8rz6IyhljNa4pxTxT746UjiGlCPb8ZILloQPy0AF56kDGX_1p8wz_Dj0Db4_ArfNG_XD_KQeZAaseaMIoIU31CxLQw0s</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1942142864</pqid></control><display><type>article</type><title>Cognitive Function of Artemisia argyi H. Fermented by Monascus purpureus under TMT-Induced Learning and Memory Deficits in ICR Mice</title><source>PubMed (Medline)</source><source>Wiley Online Library Open Access</source><source>Alma/SFX Local Collection</source><source>EZB Electronic Journals Library</source><source>PubMed Central Open Access</source><creator>Heo, Ho Jin ; Ha, Gi Jeong ; Kim, Jong Min ; Ha, Jeong Su ; Park, Seon Kyeong ; Lee, Du Sang ; Kang, Jin Yong ; Seo, Weon Taek</creator><contributor>Kim, Youn C.</contributor><creatorcontrib>Heo, Ho Jin ; Ha, Gi Jeong ; Kim, Jong Min ; Ha, Jeong Su ; Park, Seon Kyeong ; Lee, Du Sang ; Kang, Jin Yong ; Seo, Weon Taek ; Kim, Youn C.</creatorcontrib><description>The cognitive effect of Artemisia argyi H. under liquid-state fermentation by Monascus purpureus (AAFM), which has cellular antioxidant activity and neuronal cell viability, on trimethyltin- (TMT-) induced learning and memory impairment in Institute of Cancer Research (ICR) mice was confirmed. Tests were conducted to determine the neuroprotective effects against H2O2-induced oxidative stress, and the results showed that AAFM has protective effects through the repression of mitochondrial injury and cellular membrane damage against H2O2-induced neurotoxicity. In animal experiments, such as the Y-maze, passive avoidance, and Morris water maze tests, AAFM also showed excellent ameliorating effects on TMT-induced cognitive dysfunction. After behavioral tests, brain tissues were extracted to assess damage to brain tissue. According to the experimental results, AAFM improved the cholinergic system by upregulating acetylcholine (ACh) contents and inhibiting acetylcholinesterase (AChE) activity. AAFM effectively improved the decline of the superoxide dismutase (SOD) level and the increase of the oxidized glutathione (GSH) ratio and lipid peroxidation (malondialdehyde (MDA) production) caused by TMT-induced oxidative stress. The occurrence of mitochondrial dysfunction and apoptosis was also decreased compared with the TMT group. Finally, quinic acid derivatives were identified as the major phenolic compounds in AAFM using ultra-performance liquid chromatography quadrupole-time-of-flight (UPLC-Q-TOF) MS analysis.</description><identifier>ISSN: 1741-427X</identifier><identifier>EISSN: 1741-4288</identifier><identifier>DOI: 10.1155/2017/5809370</identifier><identifier>PMID: 29081819</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Acetylcholinesterase ; Alzheimer's disease ; Animal research ; Animal tissues ; Antioxidants ; Apoptosis ; Biochemistry ; Brain ; Brain injury ; Cancer ; Cholinergic transmission ; Cognitive ability ; Cytochrome ; Fermentation ; Fungi ; Genetic aspects ; Glutathione ; Hydrogen peroxide ; Learning ; Life sciences ; Lipid peroxidation ; Liquid chromatography ; Malondialdehyde ; Memory ; Microorganisms ; Mitochondria ; Monascus purpureus ; Mugwort ; Nervous system ; Neuroprotection ; Neurotoxicity ; Oxidative stress ; Peroxidation ; Phenolic compounds ; Phenols ; Quadrupoles ; Quinic acid ; Rats ; Rattus ; Rice ; Signal transduction ; Superoxide dismutase ; Trimethyltin</subject><ispartof>Evidence-based complementary and alternative medicine, 2017-01, Vol.2017 (2017), p.1-16</ispartof><rights>Copyright © 2017 Jin Yong Kang et al.</rights><rights>COPYRIGHT 2017 John Wiley &amp; Sons, Inc.</rights><rights>Copyright © 2017 Jin Yong Kang et al.; This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2017 Jin Yong Kang et al. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-c514d8b8fd9c143c313dd4b961f5f39f070837f6c7beda004d5d9a602afd0fab3</citedby><cites>FETCH-LOGICAL-c499t-c514d8b8fd9c143c313dd4b961f5f39f070837f6c7beda004d5d9a602afd0fab3</cites><orcidid>0000-0002-3560-2007</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610803/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610803/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29081819$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Kim, Youn C.</contributor><creatorcontrib>Heo, Ho Jin</creatorcontrib><creatorcontrib>Ha, Gi Jeong</creatorcontrib><creatorcontrib>Kim, Jong Min</creatorcontrib><creatorcontrib>Ha, Jeong Su</creatorcontrib><creatorcontrib>Park, Seon Kyeong</creatorcontrib><creatorcontrib>Lee, Du Sang</creatorcontrib><creatorcontrib>Kang, Jin Yong</creatorcontrib><creatorcontrib>Seo, Weon Taek</creatorcontrib><title>Cognitive Function of Artemisia argyi H. Fermented by Monascus purpureus under TMT-Induced Learning and Memory Deficits in ICR Mice</title><title>Evidence-based complementary and alternative medicine</title><addtitle>Evid Based Complement Alternat Med</addtitle><description>The cognitive effect of Artemisia argyi H. under liquid-state fermentation by Monascus purpureus (AAFM), which has cellular antioxidant activity and neuronal cell viability, on trimethyltin- (TMT-) induced learning and memory impairment in Institute of Cancer Research (ICR) mice was confirmed. Tests were conducted to determine the neuroprotective effects against H2O2-induced oxidative stress, and the results showed that AAFM has protective effects through the repression of mitochondrial injury and cellular membrane damage against H2O2-induced neurotoxicity. In animal experiments, such as the Y-maze, passive avoidance, and Morris water maze tests, AAFM also showed excellent ameliorating effects on TMT-induced cognitive dysfunction. After behavioral tests, brain tissues were extracted to assess damage to brain tissue. According to the experimental results, AAFM improved the cholinergic system by upregulating acetylcholine (ACh) contents and inhibiting acetylcholinesterase (AChE) activity. AAFM effectively improved the decline of the superoxide dismutase (SOD) level and the increase of the oxidized glutathione (GSH) ratio and lipid peroxidation (malondialdehyde (MDA) production) caused by TMT-induced oxidative stress. The occurrence of mitochondrial dysfunction and apoptosis was also decreased compared with the TMT group. Finally, quinic acid derivatives were identified as the major phenolic compounds in AAFM using ultra-performance liquid chromatography quadrupole-time-of-flight (UPLC-Q-TOF) MS analysis.</description><subject>Acetylcholinesterase</subject><subject>Alzheimer's disease</subject><subject>Animal research</subject><subject>Animal tissues</subject><subject>Antioxidants</subject><subject>Apoptosis</subject><subject>Biochemistry</subject><subject>Brain</subject><subject>Brain injury</subject><subject>Cancer</subject><subject>Cholinergic transmission</subject><subject>Cognitive ability</subject><subject>Cytochrome</subject><subject>Fermentation</subject><subject>Fungi</subject><subject>Genetic aspects</subject><subject>Glutathione</subject><subject>Hydrogen peroxide</subject><subject>Learning</subject><subject>Life sciences</subject><subject>Lipid peroxidation</subject><subject>Liquid chromatography</subject><subject>Malondialdehyde</subject><subject>Memory</subject><subject>Microorganisms</subject><subject>Mitochondria</subject><subject>Monascus purpureus</subject><subject>Mugwort</subject><subject>Nervous system</subject><subject>Neuroprotection</subject><subject>Neurotoxicity</subject><subject>Oxidative stress</subject><subject>Peroxidation</subject><subject>Phenolic compounds</subject><subject>Phenols</subject><subject>Quadrupoles</subject><subject>Quinic acid</subject><subject>Rats</subject><subject>Rattus</subject><subject>Rice</subject><subject>Signal transduction</subject><subject>Superoxide dismutase</subject><subject>Trimethyltin</subject><issn>1741-427X</issn><issn>1741-4288</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNksGLEzEYxQdR3LV68ywBL4J2N5lJJpOLUKp1Cy2CVPAWMsmXbpaZpCYzKz37j5vS2lVPQiAf5MdLXt4ripcEXxHC2HWJCb9mDRYVx4-KS8IpmdKyaR6fZ_7toniW0h3GpeCcPy0uSoEb0hBxWfych613g7sHtBi9HlzwKFg0iwP0LjmFVNzuHbq5QguIPfgBDGr3aB28SnpMaDfGvCBPozcQ0Wa9mS69GXXmVqCid36LlDdoDX2Ie_QBrNNuSMh5tJx_QWun4XnxxKouwYvTPim-Lj5u5jfT1edPy_lsNdVUiGGqGaGmaRtrhCa00hWpjKGtqIllthIWc9xU3Naat2AUxtQwI1SNS2UNtqqtJsX7o-5ubHswOruJqpO76HoV9zIoJ_8-8e5WbsO9ZDXBDa6ywJuTQAzfR0iDzH-koeuUhzAmSQTjvOY0ZzEpXv-D3oUx-mwvU7QkOaGaPlBb1YF03oZ8rz6IyhljNa4pxTxT746UjiGlCPb8ZILloQPy0AF56kDGX_1p8wz_Dj0Db4_ArfNG_XD_KQeZAaseaMIoIU31CxLQw0s</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Heo, Ho Jin</creator><creator>Ha, Gi Jeong</creator><creator>Kim, Jong Min</creator><creator>Ha, Jeong Su</creator><creator>Park, Seon Kyeong</creator><creator>Lee, Du Sang</creator><creator>Kang, Jin Yong</creator><creator>Seo, Weon Taek</creator><general>Hindawi Publishing Corporation</general><general>Hindawi</general><general>John Wiley &amp; Sons, Inc</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7T5</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88G</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</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>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M2M</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PIMPY</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><orcidid>https://orcid.org/0000-0002-3560-2007</orcidid></search><sort><creationdate>20170101</creationdate><title>Cognitive Function of Artemisia argyi H. Fermented by Monascus purpureus under TMT-Induced Learning and Memory Deficits in ICR Mice</title><author>Heo, Ho Jin ; Ha, Gi Jeong ; Kim, Jong Min ; Ha, Jeong Su ; Park, Seon Kyeong ; Lee, Du Sang ; Kang, Jin Yong ; Seo, Weon Taek</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c499t-c514d8b8fd9c143c313dd4b961f5f39f070837f6c7beda004d5d9a602afd0fab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acetylcholinesterase</topic><topic>Alzheimer's disease</topic><topic>Animal research</topic><topic>Animal tissues</topic><topic>Antioxidants</topic><topic>Apoptosis</topic><topic>Biochemistry</topic><topic>Brain</topic><topic>Brain injury</topic><topic>Cancer</topic><topic>Cholinergic transmission</topic><topic>Cognitive ability</topic><topic>Cytochrome</topic><topic>Fermentation</topic><topic>Fungi</topic><topic>Genetic aspects</topic><topic>Glutathione</topic><topic>Hydrogen peroxide</topic><topic>Learning</topic><topic>Life sciences</topic><topic>Lipid peroxidation</topic><topic>Liquid chromatography</topic><topic>Malondialdehyde</topic><topic>Memory</topic><topic>Microorganisms</topic><topic>Mitochondria</topic><topic>Monascus purpureus</topic><topic>Mugwort</topic><topic>Nervous system</topic><topic>Neuroprotection</topic><topic>Neurotoxicity</topic><topic>Oxidative stress</topic><topic>Peroxidation</topic><topic>Phenolic compounds</topic><topic>Phenols</topic><topic>Quadrupoles</topic><topic>Quinic acid</topic><topic>Rats</topic><topic>Rattus</topic><topic>Rice</topic><topic>Signal transduction</topic><topic>Superoxide dismutase</topic><topic>Trimethyltin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Heo, Ho Jin</creatorcontrib><creatorcontrib>Ha, Gi Jeong</creatorcontrib><creatorcontrib>Kim, Jong Min</creatorcontrib><creatorcontrib>Ha, Jeong Su</creatorcontrib><creatorcontrib>Park, Seon Kyeong</creatorcontrib><creatorcontrib>Lee, Du Sang</creatorcontrib><creatorcontrib>Kang, Jin Yong</creatorcontrib><creatorcontrib>Seo, Weon Taek</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing &amp; Allied Health Database</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Psychology Database (ProQuest)</collection><collection>ProQuest Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Evidence-based complementary and alternative medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Heo, Ho Jin</au><au>Ha, Gi Jeong</au><au>Kim, Jong Min</au><au>Ha, Jeong Su</au><au>Park, Seon Kyeong</au><au>Lee, Du Sang</au><au>Kang, Jin Yong</au><au>Seo, Weon Taek</au><au>Kim, Youn C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cognitive Function of Artemisia argyi H. Fermented by Monascus purpureus under TMT-Induced Learning and Memory Deficits in ICR Mice</atitle><jtitle>Evidence-based complementary and alternative medicine</jtitle><addtitle>Evid Based Complement Alternat Med</addtitle><date>2017-01-01</date><risdate>2017</risdate><volume>2017</volume><issue>2017</issue><spage>1</spage><epage>16</epage><pages>1-16</pages><issn>1741-427X</issn><eissn>1741-4288</eissn><abstract>The cognitive effect of Artemisia argyi H. under liquid-state fermentation by Monascus purpureus (AAFM), which has cellular antioxidant activity and neuronal cell viability, on trimethyltin- (TMT-) induced learning and memory impairment in Institute of Cancer Research (ICR) mice was confirmed. Tests were conducted to determine the neuroprotective effects against H2O2-induced oxidative stress, and the results showed that AAFM has protective effects through the repression of mitochondrial injury and cellular membrane damage against H2O2-induced neurotoxicity. In animal experiments, such as the Y-maze, passive avoidance, and Morris water maze tests, AAFM also showed excellent ameliorating effects on TMT-induced cognitive dysfunction. After behavioral tests, brain tissues were extracted to assess damage to brain tissue. According to the experimental results, AAFM improved the cholinergic system by upregulating acetylcholine (ACh) contents and inhibiting acetylcholinesterase (AChE) activity. AAFM effectively improved the decline of the superoxide dismutase (SOD) level and the increase of the oxidized glutathione (GSH) ratio and lipid peroxidation (malondialdehyde (MDA) production) caused by TMT-induced oxidative stress. The occurrence of mitochondrial dysfunction and apoptosis was also decreased compared with the TMT group. Finally, quinic acid derivatives were identified as the major phenolic compounds in AAFM using ultra-performance liquid chromatography quadrupole-time-of-flight (UPLC-Q-TOF) MS analysis.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>29081819</pmid><doi>10.1155/2017/5809370</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0002-3560-2007</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1741-427X
ispartof Evidence-based complementary and alternative medicine, 2017-01, Vol.2017 (2017), p.1-16
issn 1741-427X
1741-4288
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5610803
source PubMed (Medline); Wiley Online Library Open Access; Alma/SFX Local Collection; EZB Electronic Journals Library; PubMed Central Open Access
subjects Acetylcholinesterase
Alzheimer's disease
Animal research
Animal tissues
Antioxidants
Apoptosis
Biochemistry
Brain
Brain injury
Cancer
Cholinergic transmission
Cognitive ability
Cytochrome
Fermentation
Fungi
Genetic aspects
Glutathione
Hydrogen peroxide
Learning
Life sciences
Lipid peroxidation
Liquid chromatography
Malondialdehyde
Memory
Microorganisms
Mitochondria
Monascus purpureus
Mugwort
Nervous system
Neuroprotection
Neurotoxicity
Oxidative stress
Peroxidation
Phenolic compounds
Phenols
Quadrupoles
Quinic acid
Rats
Rattus
Rice
Signal transduction
Superoxide dismutase
Trimethyltin
title Cognitive Function of Artemisia argyi H. Fermented by Monascus purpureus under TMT-Induced Learning and Memory Deficits in ICR Mice
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-11T19%3A30%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cognitive%20Function%20of%20Artemisia%20argyi%20H.%20Fermented%20by%20Monascus%20purpureus%20under%20TMT-Induced%20Learning%20and%20Memory%20Deficits%20in%20ICR%20Mice&rft.jtitle=Evidence-based%20complementary%20and%20alternative%20medicine&rft.au=Heo,%20Ho%20Jin&rft.date=2017-01-01&rft.volume=2017&rft.issue=2017&rft.spage=1&rft.epage=16&rft.pages=1-16&rft.issn=1741-427X&rft.eissn=1741-4288&rft_id=info:doi/10.1155/2017/5809370&rft_dat=%3Cgale_pubme%3EA556064407%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1942142864&rft_id=info:pmid/29081819&rft_galeid=A556064407&rfr_iscdi=true