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Targeted and non-targeted metabolic characteristics of 6,7-dihydroxy-2,4- dimethoxyphenanthrene during simulated gastrointestinal digestion
6,7-dihydroxy-2,4-dimethoxyphenanthrene (PC4), isolated and identified from Chinese yam, was one of the important characteristic active ingredients. The present study established simulated gastrointestinal digestion and caco-2 intestinal epithelial models to investigate the digestive and metabolic c...
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Published in: | Food chemistry 2025-02, Vol.464 (Pt 1), p.141534, Article 141534 |
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creator | Li, Qian Liu, Fan Liao, Sentai Zhou, Donglai Xing, Dongxu Zou, Yuxiao |
description | 6,7-dihydroxy-2,4-dimethoxyphenanthrene (PC4), isolated and identified from Chinese yam, was one of the important characteristic active ingredients. The present study established simulated gastrointestinal digestion and caco-2 intestinal epithelial models to investigate the digestive and metabolic characteristics of PC4. The results indicated that PC4 was mainly digested and metabolized in the intestine, with a digestion rate of 94 %, producing active characteristic metabolites including 2,6-dimethoxy-4-phenanthrenol (MC1) and 1-methoxyphenanthrene (MC2). Molecular docking indicated that the COX-2 enzyme inhibitory activity of MC1 might be superior to that of the prototype PC4. During 24 h co-incubation of PC4 with caco-2 monolayer epithelial, the signal pathway related to lipid decomposition was up-regulated within 0–12 h, while the diabetes complications AGE-RAGE was inhibited just in 0–6 h period significantly. The research database provided scientific basis for the digestion and metabolism of PC4, and laid theoretical foundation for the scientific development of Chinese yam functional foods.
[Display omitted]
•PC4 was mainly digested and metabolized in intestine, with a digestion rate of 94 %.•Characteristic metabolites including MC1 and MC2 were produced.•COX-2 inhibitory activity of MC1 might be superior to that of the prototype PC4.•Metabolites affected signaling pathways related to lipid decomposition and diabetes. |
doi_str_mv | 10.1016/j.foodchem.2024.141534 |
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[Display omitted]
•PC4 was mainly digested and metabolized in intestine, with a digestion rate of 94 %.•Characteristic metabolites including MC1 and MC2 were produced.•COX-2 inhibitory activity of MC1 might be superior to that of the prototype PC4.•Metabolites affected signaling pathways related to lipid decomposition and diabetes.</description><identifier>ISSN: 0308-8146</identifier><identifier>ISSN: 1873-7072</identifier><identifier>EISSN: 1873-7072</identifier><identifier>DOI: 10.1016/j.foodchem.2024.141534</identifier><identifier>PMID: 39396477</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Administration, Oral ; Caco-2 Cells ; Characteristic metabolism ; Chinese yam ; Cyclooxygenase 2 - metabolism ; Cyclooxygenase 2 Inhibitors - pharmacology ; Databases, Genetic ; Digestion - drug effects ; Digestion - physiology ; Dioscorea - chemistry ; Dioscorea - metabolism ; Functional Food ; Gastrointestinal digestion ; Gastrointestinal Tract - drug effects ; Gastrointestinal Tract - metabolism ; Humans ; Japan ; Molecular Docking Simulation ; Phenanthrenes ; Principal Component Analysis ; Signal Transduction - drug effects ; Time Factors</subject><ispartof>Food chemistry, 2025-02, Vol.464 (Pt 1), p.141534, Article 141534</ispartof><rights>2024 Elsevier Ltd</rights><rights>Copyright © 2024 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c245t-d47272de3c4def5f29738fe335cdf9be75d1bb40a46178a0ccea3f32b107e9a93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39396477$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Qian</creatorcontrib><creatorcontrib>Liu, Fan</creatorcontrib><creatorcontrib>Liao, Sentai</creatorcontrib><creatorcontrib>Zhou, Donglai</creatorcontrib><creatorcontrib>Xing, Dongxu</creatorcontrib><creatorcontrib>Zou, Yuxiao</creatorcontrib><title>Targeted and non-targeted metabolic characteristics of 6,7-dihydroxy-2,4- dimethoxyphenanthrene during simulated gastrointestinal digestion</title><title>Food chemistry</title><addtitle>Food Chem</addtitle><description>6,7-dihydroxy-2,4-dimethoxyphenanthrene (PC4), isolated and identified from Chinese yam, was one of the important characteristic active ingredients. The present study established simulated gastrointestinal digestion and caco-2 intestinal epithelial models to investigate the digestive and metabolic characteristics of PC4. The results indicated that PC4 was mainly digested and metabolized in the intestine, with a digestion rate of 94 %, producing active characteristic metabolites including 2,6-dimethoxy-4-phenanthrenol (MC1) and 1-methoxyphenanthrene (MC2). Molecular docking indicated that the COX-2 enzyme inhibitory activity of MC1 might be superior to that of the prototype PC4. During 24 h co-incubation of PC4 with caco-2 monolayer epithelial, the signal pathway related to lipid decomposition was up-regulated within 0–12 h, while the diabetes complications AGE-RAGE was inhibited just in 0–6 h period significantly. The research database provided scientific basis for the digestion and metabolism of PC4, and laid theoretical foundation for the scientific development of Chinese yam functional foods.
[Display omitted]
•PC4 was mainly digested and metabolized in intestine, with a digestion rate of 94 %.•Characteristic metabolites including MC1 and MC2 were produced.•COX-2 inhibitory activity of MC1 might be superior to that of the prototype PC4.•Metabolites affected signaling pathways related to lipid decomposition and diabetes.</description><subject>Administration, Oral</subject><subject>Caco-2 Cells</subject><subject>Characteristic metabolism</subject><subject>Chinese yam</subject><subject>Cyclooxygenase 2 - metabolism</subject><subject>Cyclooxygenase 2 Inhibitors - pharmacology</subject><subject>Databases, Genetic</subject><subject>Digestion - drug effects</subject><subject>Digestion - physiology</subject><subject>Dioscorea - chemistry</subject><subject>Dioscorea - metabolism</subject><subject>Functional Food</subject><subject>Gastrointestinal digestion</subject><subject>Gastrointestinal Tract - drug effects</subject><subject>Gastrointestinal Tract - metabolism</subject><subject>Humans</subject><subject>Japan</subject><subject>Molecular Docking Simulation</subject><subject>Phenanthrenes</subject><subject>Principal Component Analysis</subject><subject>Signal Transduction - drug effects</subject><subject>Time Factors</subject><issn>0308-8146</issn><issn>1873-7072</issn><issn>1873-7072</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><recordid>eNqFUctu1DAUtRCITgu_UGXJoh78SpzsQFWBSpXYlLXl2NcTjxJ7sB3EfAM_jUfTYcvqPnQeuvcgdEvJlhLafdxvXYzWTLBsGWFiSwVtuXiFNrSXHEsi2Wu0IZz0uKeiu0LXOe8JIYzQ_i264gMfOiHlBv151mkHBWyjg21CDLhcFgsUPcbZm8ZMOmlTIPlcvMlNdE13J7H109Gm-PuI2Z3AjfWVMdXxMEHQoUwJAjR2TT7smuyXddYn2Z3OJUUfClSxoOfK253aGN6hN07PGd6_1Bv048vD8_03_PT96-P95ydsmGgLtkIyySxwIyy41rFB8t4B562xbhhBtpaOoyBadFT2mhgDmjvORkokDHrgN-jDWfeQ4s-1eqvFZwPzrAPENStOace5YF1fod0ZalLMOYFTh-QXnY6KEnUKQu3VJQh1CkKdg6jE2xePdVzA_qNdPl8Bn84AqJf-8pBUNh6CAesTmKJs9P_z-AsM4KD1</recordid><startdate>20250201</startdate><enddate>20250201</enddate><creator>Li, Qian</creator><creator>Liu, Fan</creator><creator>Liao, Sentai</creator><creator>Zhou, Donglai</creator><creator>Xing, Dongxu</creator><creator>Zou, Yuxiao</creator><general>Elsevier Ltd</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>7X8</scope></search><sort><creationdate>20250201</creationdate><title>Targeted and non-targeted metabolic characteristics of 6,7-dihydroxy-2,4- dimethoxyphenanthrene during simulated gastrointestinal digestion</title><author>Li, Qian ; Liu, Fan ; Liao, Sentai ; Zhou, Donglai ; Xing, Dongxu ; Zou, Yuxiao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c245t-d47272de3c4def5f29738fe335cdf9be75d1bb40a46178a0ccea3f32b107e9a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>Administration, Oral</topic><topic>Caco-2 Cells</topic><topic>Characteristic metabolism</topic><topic>Chinese yam</topic><topic>Cyclooxygenase 2 - metabolism</topic><topic>Cyclooxygenase 2 Inhibitors - pharmacology</topic><topic>Databases, Genetic</topic><topic>Digestion - drug effects</topic><topic>Digestion - physiology</topic><topic>Dioscorea - chemistry</topic><topic>Dioscorea - metabolism</topic><topic>Functional Food</topic><topic>Gastrointestinal digestion</topic><topic>Gastrointestinal Tract - drug effects</topic><topic>Gastrointestinal Tract - metabolism</topic><topic>Humans</topic><topic>Japan</topic><topic>Molecular Docking Simulation</topic><topic>Phenanthrenes</topic><topic>Principal Component Analysis</topic><topic>Signal Transduction - drug effects</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Qian</creatorcontrib><creatorcontrib>Liu, Fan</creatorcontrib><creatorcontrib>Liao, Sentai</creatorcontrib><creatorcontrib>Zhou, Donglai</creatorcontrib><creatorcontrib>Xing, Dongxu</creatorcontrib><creatorcontrib>Zou, Yuxiao</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>Food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Qian</au><au>Liu, Fan</au><au>Liao, Sentai</au><au>Zhou, Donglai</au><au>Xing, Dongxu</au><au>Zou, Yuxiao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Targeted and non-targeted metabolic characteristics of 6,7-dihydroxy-2,4- dimethoxyphenanthrene during simulated gastrointestinal digestion</atitle><jtitle>Food chemistry</jtitle><addtitle>Food Chem</addtitle><date>2025-02-01</date><risdate>2025</risdate><volume>464</volume><issue>Pt 1</issue><spage>141534</spage><pages>141534-</pages><artnum>141534</artnum><issn>0308-8146</issn><issn>1873-7072</issn><eissn>1873-7072</eissn><abstract>6,7-dihydroxy-2,4-dimethoxyphenanthrene (PC4), isolated and identified from Chinese yam, was one of the important characteristic active ingredients. The present study established simulated gastrointestinal digestion and caco-2 intestinal epithelial models to investigate the digestive and metabolic characteristics of PC4. The results indicated that PC4 was mainly digested and metabolized in the intestine, with a digestion rate of 94 %, producing active characteristic metabolites including 2,6-dimethoxy-4-phenanthrenol (MC1) and 1-methoxyphenanthrene (MC2). Molecular docking indicated that the COX-2 enzyme inhibitory activity of MC1 might be superior to that of the prototype PC4. During 24 h co-incubation of PC4 with caco-2 monolayer epithelial, the signal pathway related to lipid decomposition was up-regulated within 0–12 h, while the diabetes complications AGE-RAGE was inhibited just in 0–6 h period significantly. The research database provided scientific basis for the digestion and metabolism of PC4, and laid theoretical foundation for the scientific development of Chinese yam functional foods.
[Display omitted]
•PC4 was mainly digested and metabolized in intestine, with a digestion rate of 94 %.•Characteristic metabolites including MC1 and MC2 were produced.•COX-2 inhibitory activity of MC1 might be superior to that of the prototype PC4.•Metabolites affected signaling pathways related to lipid decomposition and diabetes.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>39396477</pmid><doi>10.1016/j.foodchem.2024.141534</doi></addata></record> |
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subjects | Administration, Oral Caco-2 Cells Characteristic metabolism Chinese yam Cyclooxygenase 2 - metabolism Cyclooxygenase 2 Inhibitors - pharmacology Databases, Genetic Digestion - drug effects Digestion - physiology Dioscorea - chemistry Dioscorea - metabolism Functional Food Gastrointestinal digestion Gastrointestinal Tract - drug effects Gastrointestinal Tract - metabolism Humans Japan Molecular Docking Simulation Phenanthrenes Principal Component Analysis Signal Transduction - drug effects Time Factors |
title | Targeted and non-targeted metabolic characteristics of 6,7-dihydroxy-2,4- dimethoxyphenanthrene during simulated gastrointestinal digestion |
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