Hypoglycemic activity of immature persimmon (Diospyros kaki Thunb.) extracts and its inhibition mechanism for α-amylase and α-glucosidase
Persimmon tannins, particularly in immature persimmons, haven't yet received corresponding attention to research on therapy of diabetes mellitus in spite of high hypoglycemic activity. To accurately screening key hypoglycemic components, immature persimmon extracts were isolated and identified...
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creator | Han, Zixuan Ren, Weiwei Liu, Xiaojuan Lin, Nan Qu, Jialin Duan, Xuchang Liu, Bin |
description | Persimmon tannins, particularly in immature persimmons, haven't yet received corresponding attention to research on therapy of diabetes mellitus in spite of high hypoglycemic activity. To accurately screening key hypoglycemic components, immature persimmon extracts were isolated and identified using enzyme affinity ultrafiltration and HRLC-ESI-MS/MS. Among them, Hederagenin (IC
= 0.077 ± 0.003 mg/mL), Ursolic acid (IC
= 0.001 ± 0.000 mg/mL) and Quercetin dehydrate (IC
= 0.081 ± 0.001 mg/mL) exhibited the strongest inhibitory effect on α-amylase (HSA and PPA) and α-glucosidase, respectively. And their inhibition mechanisms were analyzed using multi-spectral analysis, atomic force microscope and molecular docking, indicating the bonding with starch digestion enzymes through hydrogen bonding and hydrophobic interaction, and generating the enzyme aggregation. In vivo starch-tolerance experiment further verified that these inhibitors could improve postprandial hyperglycemia (17.18 % ∼ 40.29 %), far more than acarbose. Suppressing, Hederagenin and Ursolic acid as triterpenoids appeared amazing potentiality to alleviate postprandial hyperglycemia, which suggested that IPE were comprehensive exploration values on prevention and treatment of hyperglycemia. |
doi_str_mv | 10.1016/j.ijbiomac.2023.128616 |
format | Article |
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= 0.077 ± 0.003 mg/mL), Ursolic acid (IC
= 0.001 ± 0.000 mg/mL) and Quercetin dehydrate (IC
= 0.081 ± 0.001 mg/mL) exhibited the strongest inhibitory effect on α-amylase (HSA and PPA) and α-glucosidase, respectively. And their inhibition mechanisms were analyzed using multi-spectral analysis, atomic force microscope and molecular docking, indicating the bonding with starch digestion enzymes through hydrogen bonding and hydrophobic interaction, and generating the enzyme aggregation. In vivo starch-tolerance experiment further verified that these inhibitors could improve postprandial hyperglycemia (17.18 % ∼ 40.29 %), far more than acarbose. Suppressing, Hederagenin and Ursolic acid as triterpenoids appeared amazing potentiality to alleviate postprandial hyperglycemia, which suggested that IPE were comprehensive exploration values on prevention and treatment of hyperglycemia.</description><identifier>ISSN: 0141-8130</identifier><identifier>EISSN: 1879-0003</identifier><identifier>DOI: 10.1016/j.ijbiomac.2023.128616</identifier><identifier>PMID: 38070815</identifier><language>eng</language><publisher>Netherlands</publisher><subject>alpha-Amylases ; alpha-Glucosidases ; Diospyros - chemistry ; Glycoside Hydrolase Inhibitors - pharmacology ; Hyperglycemia ; Hypoglycemic Agents - chemistry ; Hypoglycemic Agents - pharmacology ; Molecular Docking Simulation ; Oleanolic Acid - analogs & derivatives ; Plant Extracts - chemistry ; Plant Extracts - pharmacology ; Starch ; Tandem Mass Spectrometry</subject><ispartof>International journal of biological macromolecules, 2024-02, Vol.257 (Pt 2), p.128616-128616, Article 128616</ispartof><rights>Copyright © 2023 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c311t-b47f5e7ea65d5b6d38720e9b385b91d1a13b16609087e0a00523548b7ca37b953</citedby><cites>FETCH-LOGICAL-c311t-b47f5e7ea65d5b6d38720e9b385b91d1a13b16609087e0a00523548b7ca37b953</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38070815$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Han, Zixuan</creatorcontrib><creatorcontrib>Ren, Weiwei</creatorcontrib><creatorcontrib>Liu, Xiaojuan</creatorcontrib><creatorcontrib>Lin, Nan</creatorcontrib><creatorcontrib>Qu, Jialin</creatorcontrib><creatorcontrib>Duan, Xuchang</creatorcontrib><creatorcontrib>Liu, Bin</creatorcontrib><title>Hypoglycemic activity of immature persimmon (Diospyros kaki Thunb.) extracts and its inhibition mechanism for α-amylase and α-glucosidase</title><title>International journal of biological macromolecules</title><addtitle>Int J Biol Macromol</addtitle><description>Persimmon tannins, particularly in immature persimmons, haven't yet received corresponding attention to research on therapy of diabetes mellitus in spite of high hypoglycemic activity. To accurately screening key hypoglycemic components, immature persimmon extracts were isolated and identified using enzyme affinity ultrafiltration and HRLC-ESI-MS/MS. Among them, Hederagenin (IC
= 0.077 ± 0.003 mg/mL), Ursolic acid (IC
= 0.001 ± 0.000 mg/mL) and Quercetin dehydrate (IC
= 0.081 ± 0.001 mg/mL) exhibited the strongest inhibitory effect on α-amylase (HSA and PPA) and α-glucosidase, respectively. And their inhibition mechanisms were analyzed using multi-spectral analysis, atomic force microscope and molecular docking, indicating the bonding with starch digestion enzymes through hydrogen bonding and hydrophobic interaction, and generating the enzyme aggregation. In vivo starch-tolerance experiment further verified that these inhibitors could improve postprandial hyperglycemia (17.18 % ∼ 40.29 %), far more than acarbose. Suppressing, Hederagenin and Ursolic acid as triterpenoids appeared amazing potentiality to alleviate postprandial hyperglycemia, which suggested that IPE were comprehensive exploration values on prevention and treatment of hyperglycemia.</description><subject>alpha-Amylases</subject><subject>alpha-Glucosidases</subject><subject>Diospyros - chemistry</subject><subject>Glycoside Hydrolase Inhibitors - pharmacology</subject><subject>Hyperglycemia</subject><subject>Hypoglycemic Agents - chemistry</subject><subject>Hypoglycemic Agents - pharmacology</subject><subject>Molecular Docking Simulation</subject><subject>Oleanolic Acid - analogs & derivatives</subject><subject>Plant Extracts - chemistry</subject><subject>Plant Extracts - pharmacology</subject><subject>Starch</subject><subject>Tandem Mass Spectrometry</subject><issn>0141-8130</issn><issn>1879-0003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9Uctu1TAUtBCIXgq_UHlZFgnnxNePLFF5FKkSm7K2bMfp9W0chzhB5Bv4Gn6Eb8LltqxGM5o5R-cMIRcINQKKd8c6HG1I0bi6gYbV2CiB4hnZoZJtBQDsOdkB7rFSyOCMvMr5WFTBUb0kZ0yBBIV8R35db1O6GzbnY3DUuCX8CMtGU09DjGZZZ08nP-dC0kgvP4SUp21Omd6b-0BvD-to67fU_1zmEs3UjB0NBcN4CDYsoWSidwczhhxpn2b653dl4jaY7P95C70bVpdy6Ir0mrzozZD9m0c8J98-fby9uq5uvn7-cvX-pnIMcansXvbcS28E77gVHVOyAd9aprhtsUODzKIQ0IKSHgwAbxjfKyudYdK2nJ2Ty9PcaU7fV58XHUN2fhjM6NOaddNC0wpkEotVnKyuHJ1n3-tpDtHMm0bQD0Xoo34qQj8UoU9FlODF447VRt_9jz19nv0Fpw2KTg</recordid><startdate>202402</startdate><enddate>202402</enddate><creator>Han, Zixuan</creator><creator>Ren, Weiwei</creator><creator>Liu, Xiaojuan</creator><creator>Lin, Nan</creator><creator>Qu, Jialin</creator><creator>Duan, Xuchang</creator><creator>Liu, Bin</creator><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>7X8</scope></search><sort><creationdate>202402</creationdate><title>Hypoglycemic activity of immature persimmon (Diospyros kaki Thunb.) extracts and its inhibition mechanism for α-amylase and α-glucosidase</title><author>Han, Zixuan ; Ren, Weiwei ; Liu, Xiaojuan ; Lin, Nan ; Qu, Jialin ; Duan, Xuchang ; Liu, Bin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c311t-b47f5e7ea65d5b6d38720e9b385b91d1a13b16609087e0a00523548b7ca37b953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>alpha-Amylases</topic><topic>alpha-Glucosidases</topic><topic>Diospyros - chemistry</topic><topic>Glycoside Hydrolase Inhibitors - pharmacology</topic><topic>Hyperglycemia</topic><topic>Hypoglycemic Agents - chemistry</topic><topic>Hypoglycemic Agents - pharmacology</topic><topic>Molecular Docking Simulation</topic><topic>Oleanolic Acid - analogs & derivatives</topic><topic>Plant Extracts - chemistry</topic><topic>Plant Extracts - pharmacology</topic><topic>Starch</topic><topic>Tandem Mass Spectrometry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Han, Zixuan</creatorcontrib><creatorcontrib>Ren, Weiwei</creatorcontrib><creatorcontrib>Liu, Xiaojuan</creatorcontrib><creatorcontrib>Lin, Nan</creatorcontrib><creatorcontrib>Qu, Jialin</creatorcontrib><creatorcontrib>Duan, Xuchang</creatorcontrib><creatorcontrib>Liu, Bin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of biological macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Han, Zixuan</au><au>Ren, Weiwei</au><au>Liu, Xiaojuan</au><au>Lin, Nan</au><au>Qu, Jialin</au><au>Duan, Xuchang</au><au>Liu, Bin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hypoglycemic activity of immature persimmon (Diospyros kaki Thunb.) extracts and its inhibition mechanism for α-amylase and α-glucosidase</atitle><jtitle>International journal of biological macromolecules</jtitle><addtitle>Int J Biol Macromol</addtitle><date>2024-02</date><risdate>2024</risdate><volume>257</volume><issue>Pt 2</issue><spage>128616</spage><epage>128616</epage><pages>128616-128616</pages><artnum>128616</artnum><issn>0141-8130</issn><eissn>1879-0003</eissn><abstract>Persimmon tannins, particularly in immature persimmons, haven't yet received corresponding attention to research on therapy of diabetes mellitus in spite of high hypoglycemic activity. To accurately screening key hypoglycemic components, immature persimmon extracts were isolated and identified using enzyme affinity ultrafiltration and HRLC-ESI-MS/MS. Among them, Hederagenin (IC
= 0.077 ± 0.003 mg/mL), Ursolic acid (IC
= 0.001 ± 0.000 mg/mL) and Quercetin dehydrate (IC
= 0.081 ± 0.001 mg/mL) exhibited the strongest inhibitory effect on α-amylase (HSA and PPA) and α-glucosidase, respectively. And their inhibition mechanisms were analyzed using multi-spectral analysis, atomic force microscope and molecular docking, indicating the bonding with starch digestion enzymes through hydrogen bonding and hydrophobic interaction, and generating the enzyme aggregation. In vivo starch-tolerance experiment further verified that these inhibitors could improve postprandial hyperglycemia (17.18 % ∼ 40.29 %), far more than acarbose. Suppressing, Hederagenin and Ursolic acid as triterpenoids appeared amazing potentiality to alleviate postprandial hyperglycemia, which suggested that IPE were comprehensive exploration values on prevention and treatment of hyperglycemia.</abstract><cop>Netherlands</cop><pmid>38070815</pmid><doi>10.1016/j.ijbiomac.2023.128616</doi><tpages>1</tpages></addata></record> |
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subjects | alpha-Amylases alpha-Glucosidases Diospyros - chemistry Glycoside Hydrolase Inhibitors - pharmacology Hyperglycemia Hypoglycemic Agents - chemistry Hypoglycemic Agents - pharmacology Molecular Docking Simulation Oleanolic Acid - analogs & derivatives Plant Extracts - chemistry Plant Extracts - pharmacology Starch Tandem Mass Spectrometry |
title | Hypoglycemic activity of immature persimmon (Diospyros kaki Thunb.) extracts and its inhibition mechanism for α-amylase and α-glucosidase |
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