Orally Administered Delphinidin 3-Rutinoside and Cyanidin 3-Rutinoside Are Directly Absorbed in Rats and Humans and Appear in the Blood as the Intact Forms
Four components of black currant anthocyanins (BCA), delphinidin 3-O-β-rutinoside (D3R), cyanidin 3-O-β-rutinoside (C3R), delphinidin 3-O-β-glucoside (D3G), and cyanidin 3-O-β-glucoside (C3G), were found to be directly absorbed and distributed to the blood and excreted into urine as the glycosylated...
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Veröffentlicht in: | Journal of agricultural and food chemistry 2001-03, Vol.49 (3), p.1546-1551 |
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creator | Matsumoto, Hitoshi Inaba, Hiromi Kishi, Mitsuo Tominaga, Shigeru Hirayama, Masao Tsuda, Takanori |
description | Four components of black currant anthocyanins (BCA), delphinidin 3-O-β-rutinoside (D3R), cyanidin 3-O-β-rutinoside (C3R), delphinidin 3-O-β-glucoside (D3G), and cyanidin 3-O-β-glucoside (C3G), were found to be directly absorbed and distributed to the blood and excreted into urine as the glycosylated forms. In a rat study, following oral administration of purified D3R, C3R, and C3G (800 μmol/kg of body weight), the anthocyanins were detected in the plasma and the C max values were 580 ± 410, 850 ± 120, and 840 ± 190 nmol/L, respectively, 0.5−2.0 h after administration. In a human study, when a mixtue of BCA [6.24 μmol (3.58 mg) consisting of 2.75 μmol (1.68 mg) of D3R, 2.08 μmol (1.24 mg) of C3R, 1.04 μmol (0.488 mg) of D3G, and 0.37 μmol (0.165 mg) of C3G/kg of body weight)] was orally ingested by eight volunteers, D3R, C3R, D3G, and C3G were detected in the plasma and urine. The plasma C max values were 73.4 ± 35.0, 46.3 ± 22.5, 22.7 ± 12.4, and 5.0 ± 3.7 nmol/L, respectively, 1.25−1.75 h after intake, and the cumulative excretion of the four compounds in urine in the period 0−8 h after intake was 0.11 ± 0.05% of the dose ingested. These results indicate that 3-O-β-rutinosyl anthocyanins were directly absorbed and distributed to the blood. Keywords: Anthocyanins; absorption; excretion; black currant; delphinidin 3-rutinoside; cyanidin 3-rutinoside; delphinidin 3-glucoside; cyanidin 3-glucoside; human; rat |
doi_str_mv | 10.1021/jf001246q |
format | Article |
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In a rat study, following oral administration of purified D3R, C3R, and C3G (800 μmol/kg of body weight), the anthocyanins were detected in the plasma and the C max values were 580 ± 410, 850 ± 120, and 840 ± 190 nmol/L, respectively, 0.5−2.0 h after administration. In a human study, when a mixtue of BCA [6.24 μmol (3.58 mg) consisting of 2.75 μmol (1.68 mg) of D3R, 2.08 μmol (1.24 mg) of C3R, 1.04 μmol (0.488 mg) of D3G, and 0.37 μmol (0.165 mg) of C3G/kg of body weight)] was orally ingested by eight volunteers, D3R, C3R, D3G, and C3G were detected in the plasma and urine. The plasma C max values were 73.4 ± 35.0, 46.3 ± 22.5, 22.7 ± 12.4, and 5.0 ± 3.7 nmol/L, respectively, 1.25−1.75 h after intake, and the cumulative excretion of the four compounds in urine in the period 0−8 h after intake was 0.11 ± 0.05% of the dose ingested. These results indicate that 3-O-β-rutinosyl anthocyanins were directly absorbed and distributed to the blood. Keywords: Anthocyanins; absorption; excretion; black currant; delphinidin 3-rutinoside; cyanidin 3-rutinoside; delphinidin 3-glucoside; cyanidin 3-glucoside; human; rat</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/jf001246q</identifier><identifier>PMID: 11312894</identifier><identifier>CODEN: JAFCAU</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Administration, Oral ; Adult ; Animals ; Anthocyanins - administration & dosage ; Anthocyanins - blood ; Anthocyanins - pharmacokinetics ; Biological and medical sciences ; General pharmacology ; Humans ; Intestinal Absorption ; Male ; Medical sciences ; Metabolic Clearance Rate ; Middle Aged ; Pharmacokinetics. Pharmacogenetics. Drug-receptor interactions ; Pharmacology. Drug treatments ; Rats ; Rats, Wistar</subject><ispartof>Journal of agricultural and food chemistry, 2001-03, Vol.49 (3), p.1546-1551</ispartof><rights>Copyright © 2001 American Chemical Society</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a474t-4c2da710a02b00ee7e34ab1d628188afa3a766bdc3d1a08dfe77e436edcfb2ae3</citedby><cites>FETCH-LOGICAL-a474t-4c2da710a02b00ee7e34ab1d628188afa3a766bdc3d1a08dfe77e436edcfb2ae3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jf001246q$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jf001246q$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,777,781,2752,27057,27905,27906,56719,56769</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=939665$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11312894$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Matsumoto, Hitoshi</creatorcontrib><creatorcontrib>Inaba, Hiromi</creatorcontrib><creatorcontrib>Kishi, Mitsuo</creatorcontrib><creatorcontrib>Tominaga, Shigeru</creatorcontrib><creatorcontrib>Hirayama, Masao</creatorcontrib><creatorcontrib>Tsuda, Takanori</creatorcontrib><title>Orally Administered Delphinidin 3-Rutinoside and Cyanidin 3-Rutinoside Are Directly Absorbed in Rats and Humans and Appear in the Blood as the Intact Forms</title><title>Journal of agricultural and food chemistry</title><addtitle>J. Agric. Food Chem</addtitle><description>Four components of black currant anthocyanins (BCA), delphinidin 3-O-β-rutinoside (D3R), cyanidin 3-O-β-rutinoside (C3R), delphinidin 3-O-β-glucoside (D3G), and cyanidin 3-O-β-glucoside (C3G), were found to be directly absorbed and distributed to the blood and excreted into urine as the glycosylated forms. In a rat study, following oral administration of purified D3R, C3R, and C3G (800 μmol/kg of body weight), the anthocyanins were detected in the plasma and the C max values were 580 ± 410, 850 ± 120, and 840 ± 190 nmol/L, respectively, 0.5−2.0 h after administration. In a human study, when a mixtue of BCA [6.24 μmol (3.58 mg) consisting of 2.75 μmol (1.68 mg) of D3R, 2.08 μmol (1.24 mg) of C3R, 1.04 μmol (0.488 mg) of D3G, and 0.37 μmol (0.165 mg) of C3G/kg of body weight)] was orally ingested by eight volunteers, D3R, C3R, D3G, and C3G were detected in the plasma and urine. The plasma C max values were 73.4 ± 35.0, 46.3 ± 22.5, 22.7 ± 12.4, and 5.0 ± 3.7 nmol/L, respectively, 1.25−1.75 h after intake, and the cumulative excretion of the four compounds in urine in the period 0−8 h after intake was 0.11 ± 0.05% of the dose ingested. These results indicate that 3-O-β-rutinosyl anthocyanins were directly absorbed and distributed to the blood. Keywords: Anthocyanins; absorption; excretion; black currant; delphinidin 3-rutinoside; cyanidin 3-rutinoside; delphinidin 3-glucoside; cyanidin 3-glucoside; human; rat</description><subject>Administration, Oral</subject><subject>Adult</subject><subject>Animals</subject><subject>Anthocyanins - administration & dosage</subject><subject>Anthocyanins - blood</subject><subject>Anthocyanins - pharmacokinetics</subject><subject>Biological and medical sciences</subject><subject>General pharmacology</subject><subject>Humans</subject><subject>Intestinal Absorption</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metabolic Clearance Rate</subject><subject>Middle Aged</subject><subject>Pharmacokinetics. Pharmacogenetics. Drug-receptor interactions</subject><subject>Pharmacology. Drug treatments</subject><subject>Rats</subject><subject>Rats, Wistar</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0c1q3DAUBWBRWppJ2kVfoBhKC1241bVsS15OZppOIJCQpGtxLV0TT_0XyYbOs_Rlo4mH6SbQlSTup4PQYewD8G_AE_i-rTiHJM0fX7EFZAmPMwD1mi14GMYqy-GEnXq_5ZyrTPK37ARAQKKKdMH-Xjtsml20tG3d1X4kRzZaUzM8hKOtu0jEt9NYd72vLUXY2Wi1wxcmS0fRunZkxn1Y6XtXhqCgbnH0z_c2U4vdvF0OA6HbT8cHis6bvrcR-ufDZTeiGaOL3rX-HXtTYePp_WE9Y78uftyvNvHV9c_L1fIqxlSmY5yaxKIEjjwpOSeSJFIsweaJAqWwQoEyz0trhAXkylYkJaUiJ2uqMkESZ-zLnDu4_nEiP-q29oaaBjvqJ6-l5BJSDv-FoFIui0IE-HWGxvXeO6r04OoW3U4D1_vK9LGyYD8eQqeyJftPHjoK4NMBoDfYVA47U_ujK0SR51lQ8az2Jf45TtH91rkUMtP3N3ca7jar9Y1Umgf_efZovN72k-vCF7_wvCdnm7n7</recordid><startdate>20010301</startdate><enddate>20010301</enddate><creator>Matsumoto, Hitoshi</creator><creator>Inaba, Hiromi</creator><creator>Kishi, Mitsuo</creator><creator>Tominaga, Shigeru</creator><creator>Hirayama, Masao</creator><creator>Tsuda, Takanori</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><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>7U7</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20010301</creationdate><title>Orally Administered Delphinidin 3-Rutinoside and Cyanidin 3-Rutinoside Are Directly Absorbed in Rats and Humans and Appear in the Blood as the Intact Forms</title><author>Matsumoto, Hitoshi ; Inaba, Hiromi ; Kishi, Mitsuo ; Tominaga, Shigeru ; Hirayama, Masao ; Tsuda, Takanori</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a474t-4c2da710a02b00ee7e34ab1d628188afa3a766bdc3d1a08dfe77e436edcfb2ae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Administration, Oral</topic><topic>Adult</topic><topic>Animals</topic><topic>Anthocyanins - administration & dosage</topic><topic>Anthocyanins - blood</topic><topic>Anthocyanins - pharmacokinetics</topic><topic>Biological and medical sciences</topic><topic>General pharmacology</topic><topic>Humans</topic><topic>Intestinal Absorption</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metabolic Clearance Rate</topic><topic>Middle Aged</topic><topic>Pharmacokinetics. Pharmacogenetics. Drug-receptor interactions</topic><topic>Pharmacology. Drug treatments</topic><topic>Rats</topic><topic>Rats, Wistar</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matsumoto, Hitoshi</creatorcontrib><creatorcontrib>Inaba, Hiromi</creatorcontrib><creatorcontrib>Kishi, Mitsuo</creatorcontrib><creatorcontrib>Tominaga, Shigeru</creatorcontrib><creatorcontrib>Hirayama, Masao</creatorcontrib><creatorcontrib>Tsuda, Takanori</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matsumoto, Hitoshi</au><au>Inaba, Hiromi</au><au>Kishi, Mitsuo</au><au>Tominaga, Shigeru</au><au>Hirayama, Masao</au><au>Tsuda, Takanori</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Orally Administered Delphinidin 3-Rutinoside and Cyanidin 3-Rutinoside Are Directly Absorbed in Rats and Humans and Appear in the Blood as the Intact Forms</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2001-03-01</date><risdate>2001</risdate><volume>49</volume><issue>3</issue><spage>1546</spage><epage>1551</epage><pages>1546-1551</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><abstract>Four components of black currant anthocyanins (BCA), delphinidin 3-O-β-rutinoside (D3R), cyanidin 3-O-β-rutinoside (C3R), delphinidin 3-O-β-glucoside (D3G), and cyanidin 3-O-β-glucoside (C3G), were found to be directly absorbed and distributed to the blood and excreted into urine as the glycosylated forms. In a rat study, following oral administration of purified D3R, C3R, and C3G (800 μmol/kg of body weight), the anthocyanins were detected in the plasma and the C max values were 580 ± 410, 850 ± 120, and 840 ± 190 nmol/L, respectively, 0.5−2.0 h after administration. In a human study, when a mixtue of BCA [6.24 μmol (3.58 mg) consisting of 2.75 μmol (1.68 mg) of D3R, 2.08 μmol (1.24 mg) of C3R, 1.04 μmol (0.488 mg) of D3G, and 0.37 μmol (0.165 mg) of C3G/kg of body weight)] was orally ingested by eight volunteers, D3R, C3R, D3G, and C3G were detected in the plasma and urine. The plasma C max values were 73.4 ± 35.0, 46.3 ± 22.5, 22.7 ± 12.4, and 5.0 ± 3.7 nmol/L, respectively, 1.25−1.75 h after intake, and the cumulative excretion of the four compounds in urine in the period 0−8 h after intake was 0.11 ± 0.05% of the dose ingested. These results indicate that 3-O-β-rutinosyl anthocyanins were directly absorbed and distributed to the blood. Keywords: Anthocyanins; absorption; excretion; black currant; delphinidin 3-rutinoside; cyanidin 3-rutinoside; delphinidin 3-glucoside; cyanidin 3-glucoside; human; rat</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>11312894</pmid><doi>10.1021/jf001246q</doi><tpages>6</tpages></addata></record> |
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subjects | Administration, Oral Adult Animals Anthocyanins - administration & dosage Anthocyanins - blood Anthocyanins - pharmacokinetics Biological and medical sciences General pharmacology Humans Intestinal Absorption Male Medical sciences Metabolic Clearance Rate Middle Aged Pharmacokinetics. Pharmacogenetics. Drug-receptor interactions Pharmacology. Drug treatments Rats Rats, Wistar |
title | Orally Administered Delphinidin 3-Rutinoside and Cyanidin 3-Rutinoside Are Directly Absorbed in Rats and Humans and Appear in the Blood as the Intact Forms |
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