The Distribution of Glucosinolates in Different Phenotypes of Lepidium peruvianum and Their Role as Acetyl- and Butyrylcholinesterase Inhibitors-In Silico and In Vitro Studies
The aim of the study was to present the fingerprint of different tuber extracts showing glucosinolates-containing substances possibly playing an important role in preventinting dementia and other memory disorders. Different phenotypes of (Brassicaceae) tubers were analysed for their glucosinolate pr...
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creator | Tarabasz, Dominik Szczeblewski, Paweł Laskowski, Tomasz Płaziński, Wojciech Baranowska-Wójcik, Ewa Szwajgier, Dominik Kukula-Koch, Wirginia Meissner, Henry O |
description | The aim of the study was to present the fingerprint of different
tuber extracts showing glucosinolates-containing substances possibly playing an important role in preventinting dementia and other memory disorders. Different phenotypes of
(Brassicaceae) tubers were analysed for their glucosinolate profile using a liquid chromatograph coupled with mass spectrometer (HPLC-ESI-QTOF-MS/MS platform). Qualitative analysis in 50% ethanolic extracts confirmed the presence of ten compounds: aliphatic, indolyl, and aromatic glucosinolates, with glucotropaeolin being the leading one, detected at levels between 0-1.57% depending on phenotype, size, processing, and collection site. The PCA analysis showed important variations in glucosinolate content between the samples and different ratios of the detected compounds. Applied in vitro activity tests confirmed inhibitory properties of extracts and single glucosinolates against acetylcholinesterase (AChE) (15.3-28.9% for the extracts and 55.95-57.60% for individual compounds) and butyrylcholinesterase (BuChE) (71.3-77.2% for the extracts and 36.2-39.9% for individual compounds). The molecular basis for the activity of glucosinolates was explained through molecular docking studies showing that the tested metabolites interacted with tryptophan and histidine residues of the enzymes, most likely blocking their active catalytic side. Based on the obtained results and described mechanism of action, it could be concluded that glucosinolates exhibit inhibitory properties against two cholinesterases present in the synaptic cleft, which indicates that selected phenotypes of
tubers cultivated under well-defined environmental and ecological conditions may present a valuable plant material to be considered for the development of therapeutic products with memory-stimulating properties. |
doi_str_mv | 10.3390/ijms23094858 |
format | Article |
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tuber extracts showing glucosinolates-containing substances possibly playing an important role in preventinting dementia and other memory disorders. Different phenotypes of
(Brassicaceae) tubers were analysed for their glucosinolate profile using a liquid chromatograph coupled with mass spectrometer (HPLC-ESI-QTOF-MS/MS platform). Qualitative analysis in 50% ethanolic extracts confirmed the presence of ten compounds: aliphatic, indolyl, and aromatic glucosinolates, with glucotropaeolin being the leading one, detected at levels between 0-1.57% depending on phenotype, size, processing, and collection site. The PCA analysis showed important variations in glucosinolate content between the samples and different ratios of the detected compounds. Applied in vitro activity tests confirmed inhibitory properties of extracts and single glucosinolates against acetylcholinesterase (AChE) (15.3-28.9% for the extracts and 55.95-57.60% for individual compounds) and butyrylcholinesterase (BuChE) (71.3-77.2% for the extracts and 36.2-39.9% for individual compounds). The molecular basis for the activity of glucosinolates was explained through molecular docking studies showing that the tested metabolites interacted with tryptophan and histidine residues of the enzymes, most likely blocking their active catalytic side. Based on the obtained results and described mechanism of action, it could be concluded that glucosinolates exhibit inhibitory properties against two cholinesterases present in the synaptic cleft, which indicates that selected phenotypes of
tubers cultivated under well-defined environmental and ecological conditions may present a valuable plant material to be considered for the development of therapeutic products with memory-stimulating properties.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms23094858</identifier><identifier>PMID: 35563248</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Acetylcholinesterase ; Alzheimer's disease ; Butyrylcholinesterase ; Cholinesterase Inhibitors - pharmacology ; Dementia disorders ; Enzymes ; Gender ; Glucosinolates ; Glucosinolates - analysis ; High performance liquid chromatography ; Histidine ; Lepidium ; Lepidium - chemistry ; Life expectancy ; Metabolites ; Molecular docking ; Molecular Docking Simulation ; Phenotype ; Phenotypes ; Plant Extracts - chemistry ; Plant Extracts - pharmacology ; Qualitative analysis ; Synaptic cleft ; Tandem Mass Spectrometry ; Tryptophan ; Tubers</subject><ispartof>International journal of molecular sciences, 2022-04, Vol.23 (9), p.4858</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c342t-780470d6b9ac190d323486e04b6f9886dfe94090bc35c4ce766f5ae8338b4c3e3</citedby><cites>FETCH-LOGICAL-c342t-780470d6b9ac190d323486e04b6f9886dfe94090bc35c4ce766f5ae8338b4c3e3</cites><orcidid>0000-0001-6936-8733 ; 0000-0002-2718-6269 ; 0000-0002-2285-0669 ; 0000-0002-2213-9631 ; 0000-0001-9817-5631 ; 0000-0003-4868-2381 ; 0000-0001-7076-600X</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/PMC9101689/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9101689/$$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/35563248$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tarabasz, Dominik</creatorcontrib><creatorcontrib>Szczeblewski, Paweł</creatorcontrib><creatorcontrib>Laskowski, Tomasz</creatorcontrib><creatorcontrib>Płaziński, Wojciech</creatorcontrib><creatorcontrib>Baranowska-Wójcik, Ewa</creatorcontrib><creatorcontrib>Szwajgier, Dominik</creatorcontrib><creatorcontrib>Kukula-Koch, Wirginia</creatorcontrib><creatorcontrib>Meissner, Henry O</creatorcontrib><title>The Distribution of Glucosinolates in Different Phenotypes of Lepidium peruvianum and Their Role as Acetyl- and Butyrylcholinesterase Inhibitors-In Silico and In Vitro Studies</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>The aim of the study was to present the fingerprint of different
tuber extracts showing glucosinolates-containing substances possibly playing an important role in preventinting dementia and other memory disorders. Different phenotypes of
(Brassicaceae) tubers were analysed for their glucosinolate profile using a liquid chromatograph coupled with mass spectrometer (HPLC-ESI-QTOF-MS/MS platform). Qualitative analysis in 50% ethanolic extracts confirmed the presence of ten compounds: aliphatic, indolyl, and aromatic glucosinolates, with glucotropaeolin being the leading one, detected at levels between 0-1.57% depending on phenotype, size, processing, and collection site. The PCA analysis showed important variations in glucosinolate content between the samples and different ratios of the detected compounds. Applied in vitro activity tests confirmed inhibitory properties of extracts and single glucosinolates against acetylcholinesterase (AChE) (15.3-28.9% for the extracts and 55.95-57.60% for individual compounds) and butyrylcholinesterase (BuChE) (71.3-77.2% for the extracts and 36.2-39.9% for individual compounds). The molecular basis for the activity of glucosinolates was explained through molecular docking studies showing that the tested metabolites interacted with tryptophan and histidine residues of the enzymes, most likely blocking their active catalytic side. Based on the obtained results and described mechanism of action, it could be concluded that glucosinolates exhibit inhibitory properties against two cholinesterases present in the synaptic cleft, which indicates that selected phenotypes of
tubers cultivated under well-defined environmental and ecological conditions may present a valuable plant material to be considered for the development of therapeutic products with memory-stimulating properties.</description><subject>Acetylcholinesterase</subject><subject>Alzheimer's disease</subject><subject>Butyrylcholinesterase</subject><subject>Cholinesterase Inhibitors - pharmacology</subject><subject>Dementia disorders</subject><subject>Enzymes</subject><subject>Gender</subject><subject>Glucosinolates</subject><subject>Glucosinolates - analysis</subject><subject>High performance liquid chromatography</subject><subject>Histidine</subject><subject>Lepidium</subject><subject>Lepidium - chemistry</subject><subject>Life expectancy</subject><subject>Metabolites</subject><subject>Molecular docking</subject><subject>Molecular Docking Simulation</subject><subject>Phenotype</subject><subject>Phenotypes</subject><subject>Plant Extracts - chemistry</subject><subject>Plant Extracts - pharmacology</subject><subject>Qualitative analysis</subject><subject>Synaptic cleft</subject><subject>Tandem Mass Spectrometry</subject><subject>Tryptophan</subject><subject>Tubers</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkstu1TAQhiMEoqWwY40ssWFBwIkdx9kglQLlSEcC0cI2cpwJmSMfO_hSKU_FK-JeqA6s5vbp1_yaKYrnFX3DWEff4m4fakY7Lhv5oDiueF2XlIr24UF-VDwJYUdpzeqme1wcsaYRrObyuPh9OQP5gCF6HFJEZ4mbyLlJ2gW0zqgIgaDNxDSBBxvJ1xmsi-uS-5ncwoIjpj1ZwKcrVDanyo4kq6In35wBogI51RBXU95M3qe4-tXo2Rm0ECJ4FYBs7IwDRudDubHkAg1qd4Pn6gdG78hFTCNCeFo8mpQJ8OwunhTfP328PPtcbr-cb85Ot6VmvI5lKylv6SiGTumqoyOrGZcCKB_E1Ekpxgk6Tjs6aNZorqEVYmoUSMbkwDUDdlK8u9Vd0rCHUWfrXpl-8bhXfu2dwv7ficW5_-mu-q6ilZBdFnh1J-Ddr5SN9nsMGoxRFlwKfS0Ez0vKts7oy__QnUveZnvXFKMtz6fK1OtbSnsXgofpfpmK9tef0B9-QsZfHBq4h_-env0BpD-zIw</recordid><startdate>20220427</startdate><enddate>20220427</enddate><creator>Tarabasz, Dominik</creator><creator>Szczeblewski, Paweł</creator><creator>Laskowski, Tomasz</creator><creator>Płaziński, Wojciech</creator><creator>Baranowska-Wójcik, Ewa</creator><creator>Szwajgier, Dominik</creator><creator>Kukula-Koch, Wirginia</creator><creator>Meissner, Henry O</creator><general>MDPI AG</general><general>MDPI</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</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>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6936-8733</orcidid><orcidid>https://orcid.org/0000-0002-2718-6269</orcidid><orcidid>https://orcid.org/0000-0002-2285-0669</orcidid><orcidid>https://orcid.org/0000-0002-2213-9631</orcidid><orcidid>https://orcid.org/0000-0001-9817-5631</orcidid><orcidid>https://orcid.org/0000-0003-4868-2381</orcidid><orcidid>https://orcid.org/0000-0001-7076-600X</orcidid></search><sort><creationdate>20220427</creationdate><title>The Distribution of Glucosinolates in Different Phenotypes of Lepidium peruvianum and Their Role as Acetyl- and Butyrylcholinesterase Inhibitors-In Silico and In Vitro Studies</title><author>Tarabasz, Dominik ; Szczeblewski, Paweł ; Laskowski, Tomasz ; Płaziński, Wojciech ; Baranowska-Wójcik, Ewa ; Szwajgier, Dominik ; Kukula-Koch, Wirginia ; Meissner, Henry O</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c342t-780470d6b9ac190d323486e04b6f9886dfe94090bc35c4ce766f5ae8338b4c3e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Acetylcholinesterase</topic><topic>Alzheimer's disease</topic><topic>Butyrylcholinesterase</topic><topic>Cholinesterase Inhibitors - pharmacology</topic><topic>Dementia disorders</topic><topic>Enzymes</topic><topic>Gender</topic><topic>Glucosinolates</topic><topic>Glucosinolates - analysis</topic><topic>High performance liquid chromatography</topic><topic>Histidine</topic><topic>Lepidium</topic><topic>Lepidium - chemistry</topic><topic>Life expectancy</topic><topic>Metabolites</topic><topic>Molecular docking</topic><topic>Molecular Docking Simulation</topic><topic>Phenotype</topic><topic>Phenotypes</topic><topic>Plant Extracts - chemistry</topic><topic>Plant Extracts - pharmacology</topic><topic>Qualitative analysis</topic><topic>Synaptic cleft</topic><topic>Tandem Mass Spectrometry</topic><topic>Tryptophan</topic><topic>Tubers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tarabasz, Dominik</creatorcontrib><creatorcontrib>Szczeblewski, Paweł</creatorcontrib><creatorcontrib>Laskowski, Tomasz</creatorcontrib><creatorcontrib>Płaziński, Wojciech</creatorcontrib><creatorcontrib>Baranowska-Wójcik, Ewa</creatorcontrib><creatorcontrib>Szwajgier, Dominik</creatorcontrib><creatorcontrib>Kukula-Koch, Wirginia</creatorcontrib><creatorcontrib>Meissner, Henry O</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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 Edition)</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 Korea</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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</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 Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tarabasz, Dominik</au><au>Szczeblewski, Paweł</au><au>Laskowski, Tomasz</au><au>Płaziński, Wojciech</au><au>Baranowska-Wójcik, Ewa</au><au>Szwajgier, Dominik</au><au>Kukula-Koch, Wirginia</au><au>Meissner, Henry O</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Distribution of Glucosinolates in Different Phenotypes of Lepidium peruvianum and Their Role as Acetyl- and Butyrylcholinesterase Inhibitors-In Silico and In Vitro Studies</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2022-04-27</date><risdate>2022</risdate><volume>23</volume><issue>9</issue><spage>4858</spage><pages>4858-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>The aim of the study was to present the fingerprint of different
tuber extracts showing glucosinolates-containing substances possibly playing an important role in preventinting dementia and other memory disorders. Different phenotypes of
(Brassicaceae) tubers were analysed for their glucosinolate profile using a liquid chromatograph coupled with mass spectrometer (HPLC-ESI-QTOF-MS/MS platform). Qualitative analysis in 50% ethanolic extracts confirmed the presence of ten compounds: aliphatic, indolyl, and aromatic glucosinolates, with glucotropaeolin being the leading one, detected at levels between 0-1.57% depending on phenotype, size, processing, and collection site. The PCA analysis showed important variations in glucosinolate content between the samples and different ratios of the detected compounds. Applied in vitro activity tests confirmed inhibitory properties of extracts and single glucosinolates against acetylcholinesterase (AChE) (15.3-28.9% for the extracts and 55.95-57.60% for individual compounds) and butyrylcholinesterase (BuChE) (71.3-77.2% for the extracts and 36.2-39.9% for individual compounds). The molecular basis for the activity of glucosinolates was explained through molecular docking studies showing that the tested metabolites interacted with tryptophan and histidine residues of the enzymes, most likely blocking their active catalytic side. Based on the obtained results and described mechanism of action, it could be concluded that glucosinolates exhibit inhibitory properties against two cholinesterases present in the synaptic cleft, which indicates that selected phenotypes of
tubers cultivated under well-defined environmental and ecological conditions may present a valuable plant material to be considered for the development of therapeutic products with memory-stimulating properties.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>35563248</pmid><doi>10.3390/ijms23094858</doi><orcidid>https://orcid.org/0000-0001-6936-8733</orcidid><orcidid>https://orcid.org/0000-0002-2718-6269</orcidid><orcidid>https://orcid.org/0000-0002-2285-0669</orcidid><orcidid>https://orcid.org/0000-0002-2213-9631</orcidid><orcidid>https://orcid.org/0000-0001-9817-5631</orcidid><orcidid>https://orcid.org/0000-0003-4868-2381</orcidid><orcidid>https://orcid.org/0000-0001-7076-600X</orcidid><oa>free_for_read</oa></addata></record> |
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source | MDPI - Multidisciplinary Digital Publishing Institute; MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | Acetylcholinesterase Alzheimer's disease Butyrylcholinesterase Cholinesterase Inhibitors - pharmacology Dementia disorders Enzymes Gender Glucosinolates Glucosinolates - analysis High performance liquid chromatography Histidine Lepidium Lepidium - chemistry Life expectancy Metabolites Molecular docking Molecular Docking Simulation Phenotype Phenotypes Plant Extracts - chemistry Plant Extracts - pharmacology Qualitative analysis Synaptic cleft Tandem Mass Spectrometry Tryptophan Tubers |
title | The Distribution of Glucosinolates in Different Phenotypes of Lepidium peruvianum and Their Role as Acetyl- and Butyrylcholinesterase Inhibitors-In Silico and In Vitro Studies |
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