UHPLC‐Orbitrap‐Fusion‐TMS‐Based Metabolomics Study of Phenylpropionamides in the Seed of Cannabis sativa L. against Alzheimer's Disease

Phenylpropionamides in the seed of Cannabis sativa L. (PHS) have a protective effect on neuroinflammation and antioxidant activity. In this study, the UHPLC‐Orbitrap‐fusion‐TMS‐based metabolomics approach was used to analyze the serum samples and identify potential biomarkers in Streptozotocin (STZ)...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Chemistry & biodiversity 2023-05, Vol.20 (5), p.e202201047-n/a
Hauptverfasser: Wu, Dan‐Dan, Liu, Yan, Guan, Wei, Pan, Juan, Kuang, Hai‐Xue, Yang, Bing‐You
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page n/a
container_issue 5
container_start_page e202201047
container_title Chemistry & biodiversity
container_volume 20
creator Wu, Dan‐Dan
Liu, Yan
Guan, Wei
Pan, Juan
Kuang, Hai‐Xue
Yang, Bing‐You
description Phenylpropionamides in the seed of Cannabis sativa L. (PHS) have a protective effect on neuroinflammation and antioxidant activity. In this study, the UHPLC‐Orbitrap‐fusion‐TMS‐based metabolomics approach was used to analyze the serum samples and identify potential biomarkers in Streptozotocin (STZ) induced Alzheimer's disease (AD) rats. The results revealed that primary bile acid biosynthesis and taurine and hypotaurine metabolism were significantly correlated with STZ‐induced AD rats. In addition, the key enzymes in these two pathways were verified at the protein level. The levels of cysteine dioxygenase type I (CDO1), cysteine sulfinic acid decarboxylase (CSAD), cysteamine (2‐aminoethanethiol) dioxygenase (ADO), 7α‐hydroxylase (CYP7A1), and sterol 12α‐hydroxylase (CYP8B1) were the key enzymes affecting the two pathways in AD rats compared with the control group (CON). Furthermore, after a high‐dose group of phenylpropionamides in the seed of Cannabis sativa L. (PHS−H) was administrated, the levels of CDO1, CSAD, CYP7A1, and CYP8B1 were all callback. These findings demonstrate for the first time that the anti‐AD effect of PHS is associated with the regulation of primary bile acid biosynthesis and taurine and hypotaurine metabolism in STZ‐induced AD rats.
doi_str_mv 10.1002/cbdv.202201047
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2803330044</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2817232478</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3737-e1936cc380b2b6c9b87d2346b1a10443880d00de6b7570fd1a30e5cd27e3cf923</originalsourceid><addsrcrecordid>eNqFkU1vEzEQhi1ERdvAlSOyxIFeEvyRrjfHdktbpFStlJbryh-zxNV-BM9uUTjxD-A39pcwUdogceFij6znfT0zL2NvpZhIIdRH78LDRAmlhBRT84IdyEyqscxz8XJXG7XPDhHviaf3_BXb10YYpafygP26u7yZF48_f18nF_tkV1SeDxi7lorbqwWdpxYh8Cvorevqroke-aIfwpp3Fb9ZQruuV6lbkcI2MQDy2PJ-CXwBpCKksG1rXUSOto8Pls8n3H61scWen9Q_lhAbSB-Qn0UE-ug126tsjfDm6R6xu_NPt8XleH598bk4mY-9NtqMQc505r3OhVMu8zOXm0ADZU5a2sNU05xBiACZM8dGVEFaLeDYB2VA-2qm9IgdbX2p928DYF82ET3UtW2hG7BUudBai43XiL3_B73vhtRSd0RJ2qOampyoyZbyqUNMUJWrFBub1qUU5SaqchNVuYuKBO-ebAfXQNjhz9kQMNsC32MN6__YlcXp2Ze_5n8AdDWjmg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2817232478</pqid></control><display><type>article</type><title>UHPLC‐Orbitrap‐Fusion‐TMS‐Based Metabolomics Study of Phenylpropionamides in the Seed of Cannabis sativa L. against Alzheimer's Disease</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Wu, Dan‐Dan ; Liu, Yan ; Guan, Wei ; Pan, Juan ; Kuang, Hai‐Xue ; Yang, Bing‐You</creator><creatorcontrib>Wu, Dan‐Dan ; Liu, Yan ; Guan, Wei ; Pan, Juan ; Kuang, Hai‐Xue ; Yang, Bing‐You</creatorcontrib><description>Phenylpropionamides in the seed of Cannabis sativa L. (PHS) have a protective effect on neuroinflammation and antioxidant activity. In this study, the UHPLC‐Orbitrap‐fusion‐TMS‐based metabolomics approach was used to analyze the serum samples and identify potential biomarkers in Streptozotocin (STZ) induced Alzheimer's disease (AD) rats. The results revealed that primary bile acid biosynthesis and taurine and hypotaurine metabolism were significantly correlated with STZ‐induced AD rats. In addition, the key enzymes in these two pathways were verified at the protein level. The levels of cysteine dioxygenase type I (CDO1), cysteine sulfinic acid decarboxylase (CSAD), cysteamine (2‐aminoethanethiol) dioxygenase (ADO), 7α‐hydroxylase (CYP7A1), and sterol 12α‐hydroxylase (CYP8B1) were the key enzymes affecting the two pathways in AD rats compared with the control group (CON). Furthermore, after a high‐dose group of phenylpropionamides in the seed of Cannabis sativa L. (PHS−H) was administrated, the levels of CDO1, CSAD, CYP7A1, and CYP8B1 were all callback. These findings demonstrate for the first time that the anti‐AD effect of PHS is associated with the regulation of primary bile acid biosynthesis and taurine and hypotaurine metabolism in STZ‐induced AD rats.</description><identifier>ISSN: 1612-1872</identifier><identifier>EISSN: 1612-1880</identifier><identifier>DOI: 10.1002/cbdv.202201047</identifier><identifier>PMID: 37072341</identifier><language>eng</language><publisher>Switzerland: Wiley Subscription Services, Inc</publisher><subject>Alzheimer Disease - chemically induced ; Alzheimer Disease - drug therapy ; Alzheimer's disease ; Animals ; Bile Acids and Salts ; Biomarkers ; Biosynthesis ; Cannabis ; Cannabis sativa ; Cannabis sativa L ; Chromatography, High Pressure Liquid ; Cysteamine ; Cysteine ; Cysteine dioxygenase ; Enzymes ; Inflammation ; Marijuana ; Metabolism ; Metabolomics ; Neurodegenerative diseases ; phenylpropionamides ; Rats ; Steroid 12-alpha-Hydroxylase ; Streptozocin ; Taurine ; Taurine - metabolism ; Taurine - pharmacology</subject><ispartof>Chemistry &amp; biodiversity, 2023-05, Vol.20 (5), p.e202201047-n/a</ispartof><rights>2023 Wiley‐VHCA AG, Zurich, Switzerland</rights><rights>2023 Wiley-VHCA AG, Zurich, Switzerland.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3737-e1936cc380b2b6c9b87d2346b1a10443880d00de6b7570fd1a30e5cd27e3cf923</citedby><cites>FETCH-LOGICAL-c3737-e1936cc380b2b6c9b87d2346b1a10443880d00de6b7570fd1a30e5cd27e3cf923</cites><orcidid>0000-0002-2310-2750</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcbdv.202201047$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcbdv.202201047$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37072341$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Dan‐Dan</creatorcontrib><creatorcontrib>Liu, Yan</creatorcontrib><creatorcontrib>Guan, Wei</creatorcontrib><creatorcontrib>Pan, Juan</creatorcontrib><creatorcontrib>Kuang, Hai‐Xue</creatorcontrib><creatorcontrib>Yang, Bing‐You</creatorcontrib><title>UHPLC‐Orbitrap‐Fusion‐TMS‐Based Metabolomics Study of Phenylpropionamides in the Seed of Cannabis sativa L. against Alzheimer's Disease</title><title>Chemistry &amp; biodiversity</title><addtitle>Chem Biodivers</addtitle><description>Phenylpropionamides in the seed of Cannabis sativa L. (PHS) have a protective effect on neuroinflammation and antioxidant activity. In this study, the UHPLC‐Orbitrap‐fusion‐TMS‐based metabolomics approach was used to analyze the serum samples and identify potential biomarkers in Streptozotocin (STZ) induced Alzheimer's disease (AD) rats. The results revealed that primary bile acid biosynthesis and taurine and hypotaurine metabolism were significantly correlated with STZ‐induced AD rats. In addition, the key enzymes in these two pathways were verified at the protein level. The levels of cysteine dioxygenase type I (CDO1), cysteine sulfinic acid decarboxylase (CSAD), cysteamine (2‐aminoethanethiol) dioxygenase (ADO), 7α‐hydroxylase (CYP7A1), and sterol 12α‐hydroxylase (CYP8B1) were the key enzymes affecting the two pathways in AD rats compared with the control group (CON). Furthermore, after a high‐dose group of phenylpropionamides in the seed of Cannabis sativa L. (PHS−H) was administrated, the levels of CDO1, CSAD, CYP7A1, and CYP8B1 were all callback. These findings demonstrate for the first time that the anti‐AD effect of PHS is associated with the regulation of primary bile acid biosynthesis and taurine and hypotaurine metabolism in STZ‐induced AD rats.</description><subject>Alzheimer Disease - chemically induced</subject><subject>Alzheimer Disease - drug therapy</subject><subject>Alzheimer's disease</subject><subject>Animals</subject><subject>Bile Acids and Salts</subject><subject>Biomarkers</subject><subject>Biosynthesis</subject><subject>Cannabis</subject><subject>Cannabis sativa</subject><subject>Cannabis sativa L</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Cysteamine</subject><subject>Cysteine</subject><subject>Cysteine dioxygenase</subject><subject>Enzymes</subject><subject>Inflammation</subject><subject>Marijuana</subject><subject>Metabolism</subject><subject>Metabolomics</subject><subject>Neurodegenerative diseases</subject><subject>phenylpropionamides</subject><subject>Rats</subject><subject>Steroid 12-alpha-Hydroxylase</subject><subject>Streptozocin</subject><subject>Taurine</subject><subject>Taurine - metabolism</subject><subject>Taurine - pharmacology</subject><issn>1612-1872</issn><issn>1612-1880</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1vEzEQhi1ERdvAlSOyxIFeEvyRrjfHdktbpFStlJbryh-zxNV-BM9uUTjxD-A39pcwUdogceFij6znfT0zL2NvpZhIIdRH78LDRAmlhBRT84IdyEyqscxz8XJXG7XPDhHviaf3_BXb10YYpafygP26u7yZF48_f18nF_tkV1SeDxi7lorbqwWdpxYh8Cvorevqroke-aIfwpp3Fb9ZQruuV6lbkcI2MQDy2PJ-CXwBpCKksG1rXUSOto8Pls8n3H61scWen9Q_lhAbSB-Qn0UE-ug126tsjfDm6R6xu_NPt8XleH598bk4mY-9NtqMQc505r3OhVMu8zOXm0ADZU5a2sNU05xBiACZM8dGVEFaLeDYB2VA-2qm9IgdbX2p928DYF82ET3UtW2hG7BUudBai43XiL3_B73vhtRSd0RJ2qOampyoyZbyqUNMUJWrFBub1qUU5SaqchNVuYuKBO-ebAfXQNjhz9kQMNsC32MN6__YlcXp2Ze_5n8AdDWjmg</recordid><startdate>202305</startdate><enddate>202305</enddate><creator>Wu, Dan‐Dan</creator><creator>Liu, Yan</creator><creator>Guan, Wei</creator><creator>Pan, Juan</creator><creator>Kuang, Hai‐Xue</creator><creator>Yang, Bing‐You</creator><general>Wiley Subscription Services, Inc</general><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>7QO</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2310-2750</orcidid></search><sort><creationdate>202305</creationdate><title>UHPLC‐Orbitrap‐Fusion‐TMS‐Based Metabolomics Study of Phenylpropionamides in the Seed of Cannabis sativa L. against Alzheimer's Disease</title><author>Wu, Dan‐Dan ; Liu, Yan ; Guan, Wei ; Pan, Juan ; Kuang, Hai‐Xue ; Yang, Bing‐You</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3737-e1936cc380b2b6c9b87d2346b1a10443880d00de6b7570fd1a30e5cd27e3cf923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Alzheimer Disease - chemically induced</topic><topic>Alzheimer Disease - drug therapy</topic><topic>Alzheimer's disease</topic><topic>Animals</topic><topic>Bile Acids and Salts</topic><topic>Biomarkers</topic><topic>Biosynthesis</topic><topic>Cannabis</topic><topic>Cannabis sativa</topic><topic>Cannabis sativa L</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Cysteamine</topic><topic>Cysteine</topic><topic>Cysteine dioxygenase</topic><topic>Enzymes</topic><topic>Inflammation</topic><topic>Marijuana</topic><topic>Metabolism</topic><topic>Metabolomics</topic><topic>Neurodegenerative diseases</topic><topic>phenylpropionamides</topic><topic>Rats</topic><topic>Steroid 12-alpha-Hydroxylase</topic><topic>Streptozocin</topic><topic>Taurine</topic><topic>Taurine - metabolism</topic><topic>Taurine - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Dan‐Dan</creatorcontrib><creatorcontrib>Liu, Yan</creatorcontrib><creatorcontrib>Guan, Wei</creatorcontrib><creatorcontrib>Pan, Juan</creatorcontrib><creatorcontrib>Kuang, Hai‐Xue</creatorcontrib><creatorcontrib>Yang, Bing‐You</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Chemistry &amp; biodiversity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Dan‐Dan</au><au>Liu, Yan</au><au>Guan, Wei</au><au>Pan, Juan</au><au>Kuang, Hai‐Xue</au><au>Yang, Bing‐You</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>UHPLC‐Orbitrap‐Fusion‐TMS‐Based Metabolomics Study of Phenylpropionamides in the Seed of Cannabis sativa L. against Alzheimer's Disease</atitle><jtitle>Chemistry &amp; biodiversity</jtitle><addtitle>Chem Biodivers</addtitle><date>2023-05</date><risdate>2023</risdate><volume>20</volume><issue>5</issue><spage>e202201047</spage><epage>n/a</epage><pages>e202201047-n/a</pages><issn>1612-1872</issn><eissn>1612-1880</eissn><abstract>Phenylpropionamides in the seed of Cannabis sativa L. (PHS) have a protective effect on neuroinflammation and antioxidant activity. In this study, the UHPLC‐Orbitrap‐fusion‐TMS‐based metabolomics approach was used to analyze the serum samples and identify potential biomarkers in Streptozotocin (STZ) induced Alzheimer's disease (AD) rats. The results revealed that primary bile acid biosynthesis and taurine and hypotaurine metabolism were significantly correlated with STZ‐induced AD rats. In addition, the key enzymes in these two pathways were verified at the protein level. The levels of cysteine dioxygenase type I (CDO1), cysteine sulfinic acid decarboxylase (CSAD), cysteamine (2‐aminoethanethiol) dioxygenase (ADO), 7α‐hydroxylase (CYP7A1), and sterol 12α‐hydroxylase (CYP8B1) were the key enzymes affecting the two pathways in AD rats compared with the control group (CON). Furthermore, after a high‐dose group of phenylpropionamides in the seed of Cannabis sativa L. (PHS−H) was administrated, the levels of CDO1, CSAD, CYP7A1, and CYP8B1 were all callback. These findings demonstrate for the first time that the anti‐AD effect of PHS is associated with the regulation of primary bile acid biosynthesis and taurine and hypotaurine metabolism in STZ‐induced AD rats.</abstract><cop>Switzerland</cop><pub>Wiley Subscription Services, Inc</pub><pmid>37072341</pmid><doi>10.1002/cbdv.202201047</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-2310-2750</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1612-1872
ispartof Chemistry & biodiversity, 2023-05, Vol.20 (5), p.e202201047-n/a
issn 1612-1872
1612-1880
language eng
recordid cdi_proquest_miscellaneous_2803330044
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Alzheimer Disease - chemically induced
Alzheimer Disease - drug therapy
Alzheimer's disease
Animals
Bile Acids and Salts
Biomarkers
Biosynthesis
Cannabis
Cannabis sativa
Cannabis sativa L
Chromatography, High Pressure Liquid
Cysteamine
Cysteine
Cysteine dioxygenase
Enzymes
Inflammation
Marijuana
Metabolism
Metabolomics
Neurodegenerative diseases
phenylpropionamides
Rats
Steroid 12-alpha-Hydroxylase
Streptozocin
Taurine
Taurine - metabolism
Taurine - pharmacology
title UHPLC‐Orbitrap‐Fusion‐TMS‐Based Metabolomics Study of Phenylpropionamides in the Seed of Cannabis sativa L. against Alzheimer's Disease
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T22%3A53%3A17IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=UHPLC%E2%80%90Orbitrap%E2%80%90Fusion%E2%80%90TMS%E2%80%90Based%20Metabolomics%20Study%20of%20Phenylpropionamides%20in%20the%20Seed%20of%20Cannabis%20sativa%20L.%20against%20Alzheimer's%20Disease&rft.jtitle=Chemistry%20&%20biodiversity&rft.au=Wu,%20Dan%E2%80%90Dan&rft.date=2023-05&rft.volume=20&rft.issue=5&rft.spage=e202201047&rft.epage=n/a&rft.pages=e202201047-n/a&rft.issn=1612-1872&rft.eissn=1612-1880&rft_id=info:doi/10.1002/cbdv.202201047&rft_dat=%3Cproquest_cross%3E2817232478%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2817232478&rft_id=info:pmid/37072341&rfr_iscdi=true