Hesperidin Bioavailability Is Increased by the Presence of 2S-Diastereoisomer and Micronization—A Randomized, Crossover and Double-Blind Clinical Trial
Hesperidin is a flavanone abundantly found in citrus fruits for which health beneficial effects have been reported. However, hesperidin shows a low bioavailability among individuals. The aim of this study was to evaluate the effects of the micronization process and 2R- and 2S-hesperidin diastereoiso...
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Veröffentlicht in: | Nutrients 2022-06, Vol.14 (12), p.2481 |
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creator | Crescenti, Anna Caimari, Antoni Alcaide-Hidalgo, Juan María Mariné-Casadó, Roger Valls, Rosa M Companys, Judit Salamanca, Patricia Calderón-Pérez, Lorena Pla-Pagà, Laura Pedret, Anna Delpino-Rius, Antoni Herrero, Pol Samarra, Iris Arola, Lluís Solà, Rosa Del Bas, Josep M |
description | Hesperidin is a flavanone abundantly found in citrus fruits for which health beneficial effects have been reported. However, hesperidin shows a low bioavailability among individuals. The aim of this study was to evaluate the effects of the micronization process and 2R- and 2S-hesperidin diastereoisomers ratio on hesperidin bioavailability. In a first phase, thirty healthy individuals consumed 500 mL of orange juice with 345 mg of hesperidin, and the levels of hesperidin metabolites excreted in urine were determined. In the second phase, fifteen individuals with intermediate hesperidin metabolite levels excreted in urine were randomized in a crossover, postprandial and double-blind intervention study. Participants consumed 500 mg of the hesperidin-supplemented Hesperidin epimeric mixture (HEM), the micronized Hesperidin epimeric mixture (MHEM) and micronized 2S-Hesperidin (M2SH) in each study visit with 1 week of washout. Hesperidin metabolites and catabolites were determined in blood and urine obtained at different timepoints over a 24 h period. The bioavailability—relative urinary hesperidin excretion (% of hesperidin ingested)—of M2SH (70 ± 14%) formed mainly by 2S-diastereoisomer was significantly higher than the bioavailability of the MHEM (55 ± 15%) and HEM (43 ± 8.0%), which consisted of a mixture of both hesperidin diastereoisomers. Relative urinary excretion of hesperidin metabolites for MHEM (9.2 ± 1.6%) was significantly higher compared to the HEM (5.2 ± 0.81%) and M2SH (3.6 ± 1.0%). In conclusion, the bioavailability of 2S-hesperidin extract was higher compared to the standard mixture of 2S-/2R-hesperidin extract due to a greater formation of hesperidin catabolites. Furthermore, the micronization process increased hesperidin bioavailability. |
doi_str_mv | 10.3390/nu14122481 |
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However, hesperidin shows a low bioavailability among individuals. The aim of this study was to evaluate the effects of the micronization process and 2R- and 2S-hesperidin diastereoisomers ratio on hesperidin bioavailability. In a first phase, thirty healthy individuals consumed 500 mL of orange juice with 345 mg of hesperidin, and the levels of hesperidin metabolites excreted in urine were determined. In the second phase, fifteen individuals with intermediate hesperidin metabolite levels excreted in urine were randomized in a crossover, postprandial and double-blind intervention study. Participants consumed 500 mg of the hesperidin-supplemented Hesperidin epimeric mixture (HEM), the micronized Hesperidin epimeric mixture (MHEM) and micronized 2S-Hesperidin (M2SH) in each study visit with 1 week of washout. Hesperidin metabolites and catabolites were determined in blood and urine obtained at different timepoints over a 24 h period. The bioavailability—relative urinary hesperidin excretion (% of hesperidin ingested)—of M2SH (70 ± 14%) formed mainly by 2S-diastereoisomer was significantly higher than the bioavailability of the MHEM (55 ± 15%) and HEM (43 ± 8.0%), which consisted of a mixture of both hesperidin diastereoisomers. Relative urinary excretion of hesperidin metabolites for MHEM (9.2 ± 1.6%) was significantly higher compared to the HEM (5.2 ± 0.81%) and M2SH (3.6 ± 1.0%). In conclusion, the bioavailability of 2S-hesperidin extract was higher compared to the standard mixture of 2S-/2R-hesperidin extract due to a greater formation of hesperidin catabolites. Furthermore, the micronization process increased hesperidin bioavailability.</description><identifier>ISSN: 2072-6643</identifier><identifier>EISSN: 2072-6643</identifier><identifier>DOI: 10.3390/nu14122481</identifier><identifier>PMID: 35745211</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Acids ; Bioavailability ; Catabolites ; Citrus ; Citrus fruits ; Clinical trials ; Colon ; Diastereoisomers ; Diastereomers ; Double-blind studies ; Excretion ; Flavonoids ; Food research ; Fruit juices ; Hesperidin ; Intervention ; Metabolites ; Microbiota ; Mixtures ; Nutritional aspects ; Particle size ; Urine</subject><ispartof>Nutrients, 2022-06, Vol.14 (12), p.2481</ispartof><rights>COPYRIGHT 2022 MDPI AG</rights><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/). 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However, hesperidin shows a low bioavailability among individuals. The aim of this study was to evaluate the effects of the micronization process and 2R- and 2S-hesperidin diastereoisomers ratio on hesperidin bioavailability. In a first phase, thirty healthy individuals consumed 500 mL of orange juice with 345 mg of hesperidin, and the levels of hesperidin metabolites excreted in urine were determined. In the second phase, fifteen individuals with intermediate hesperidin metabolite levels excreted in urine were randomized in a crossover, postprandial and double-blind intervention study. Participants consumed 500 mg of the hesperidin-supplemented Hesperidin epimeric mixture (HEM), the micronized Hesperidin epimeric mixture (MHEM) and micronized 2S-Hesperidin (M2SH) in each study visit with 1 week of washout. Hesperidin metabolites and catabolites were determined in blood and urine obtained at different timepoints over a 24 h period. The bioavailability—relative urinary hesperidin excretion (% of hesperidin ingested)—of M2SH (70 ± 14%) formed mainly by 2S-diastereoisomer was significantly higher than the bioavailability of the MHEM (55 ± 15%) and HEM (43 ± 8.0%), which consisted of a mixture of both hesperidin diastereoisomers. Relative urinary excretion of hesperidin metabolites for MHEM (9.2 ± 1.6%) was significantly higher compared to the HEM (5.2 ± 0.81%) and M2SH (3.6 ± 1.0%). In conclusion, the bioavailability of 2S-hesperidin extract was higher compared to the standard mixture of 2S-/2R-hesperidin extract due to a greater formation of hesperidin catabolites. Furthermore, the micronization process increased hesperidin bioavailability.</description><subject>Acids</subject><subject>Bioavailability</subject><subject>Catabolites</subject><subject>Citrus</subject><subject>Citrus fruits</subject><subject>Clinical trials</subject><subject>Colon</subject><subject>Diastereoisomers</subject><subject>Diastereomers</subject><subject>Double-blind studies</subject><subject>Excretion</subject><subject>Flavonoids</subject><subject>Food research</subject><subject>Fruit juices</subject><subject>Hesperidin</subject><subject>Intervention</subject><subject>Metabolites</subject><subject>Microbiota</subject><subject>Mixtures</subject><subject>Nutritional aspects</subject><subject>Particle size</subject><subject>Urine</subject><issn>2072-6643</issn><issn>2072-6643</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNptks1u1DAQxyMEolXphSewxAUhUuKPxJsL0nYLdKUiEJSz5TjjdirH3trJSu2Jh-DC6_EkOOqqUMRY8sfMb_72yFMUz2l1xHlbvfETFZQxsaCPin1WSVY2jeCP_9rvFYcpXVWzyUo2_Gmxx2spakbpfvHzFNIGIvboyTEGvdXodIcOxxuyTmTtTQSdoCfdDRkvgXyOkMAbIMES9rU8QZ1GiBAwhQEi0b4nH9HE4PFWjxj8r-8_luRLdocBb6F_TVYxpBS2O_YkTJ2D8thhPqzyjEY7ch5Ru2fFE6tdgsPdelB8e__ufHVann36sF4tz0oj6mosDctFMWha2zXWaltpZmstuKW14JIveg5dJ9pGC8FA9L1sem6o7qiwgi1Eyw-Kt3e6m6kboDfgx6id2kQcdLxRQaN6GPF4qS7CVrWM06yQBV7uBGK4niCNasBkwDntIUxJsWZBK15XdEZf_INehSn6XF6mZCuzZLZ76kI7UOhtyPeaWVQtJWsFk7Wc3330HyqPHgY0wYPF7H-Q8OouwcxfEMHe10grNfeS-tNL_Dd5GLvp</recordid><startdate>20220601</startdate><enddate>20220601</enddate><creator>Crescenti, Anna</creator><creator>Caimari, Antoni</creator><creator>Alcaide-Hidalgo, Juan María</creator><creator>Mariné-Casadó, Roger</creator><creator>Valls, Rosa M</creator><creator>Companys, Judit</creator><creator>Salamanca, Patricia</creator><creator>Calderón-Pérez, Lorena</creator><creator>Pla-Pagà, Laura</creator><creator>Pedret, Anna</creator><creator>Delpino-Rius, Antoni</creator><creator>Herrero, Pol</creator><creator>Samarra, Iris</creator><creator>Arola, Lluís</creator><creator>Solà, Rosa</creator><creator>Del Bas, Josep M</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>COVID</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8581-0616</orcidid><orcidid>https://orcid.org/0000-0002-0700-2004</orcidid><orcidid>https://orcid.org/0000-0002-0924-4920</orcidid><orcidid>https://orcid.org/0000-0002-3383-6889</orcidid><orcidid>https://orcid.org/0000-0002-3351-0942</orcidid><orcidid>https://orcid.org/0000-0001-6144-0294</orcidid><orcidid>https://orcid.org/0000-0001-5705-7807</orcidid><orcidid>https://orcid.org/0000-0003-2767-1974</orcidid><orcidid>https://orcid.org/0000-0003-1485-0818</orcidid><orcidid>https://orcid.org/0000-0002-9606-6762</orcidid><orcidid>https://orcid.org/0000-0002-5327-932X</orcidid></search><sort><creationdate>20220601</creationdate><title>Hesperidin Bioavailability Is Increased by the Presence of 2S-Diastereoisomer and Micronization—A Randomized, Crossover and Double-Blind Clinical Trial</title><author>Crescenti, Anna ; Caimari, Antoni ; Alcaide-Hidalgo, Juan María ; Mariné-Casadó, Roger ; Valls, Rosa M ; Companys, Judit ; Salamanca, Patricia ; Calderón-Pérez, Lorena ; Pla-Pagà, Laura ; Pedret, Anna ; Delpino-Rius, Antoni ; Herrero, Pol ; Samarra, Iris ; Arola, Lluís ; Solà, Rosa ; Del Bas, Josep M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c450t-c27072e69fb6ffaf0a2f5a43f1543738d3ebb496a442e4dd76d3c1ab14f428493</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Acids</topic><topic>Bioavailability</topic><topic>Catabolites</topic><topic>Citrus</topic><topic>Citrus fruits</topic><topic>Clinical trials</topic><topic>Colon</topic><topic>Diastereoisomers</topic><topic>Diastereomers</topic><topic>Double-blind studies</topic><topic>Excretion</topic><topic>Flavonoids</topic><topic>Food research</topic><topic>Fruit juices</topic><topic>Hesperidin</topic><topic>Intervention</topic><topic>Metabolites</topic><topic>Microbiota</topic><topic>Mixtures</topic><topic>Nutritional aspects</topic><topic>Particle size</topic><topic>Urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Crescenti, Anna</creatorcontrib><creatorcontrib>Caimari, Antoni</creatorcontrib><creatorcontrib>Alcaide-Hidalgo, Juan María</creatorcontrib><creatorcontrib>Mariné-Casadó, Roger</creatorcontrib><creatorcontrib>Valls, Rosa M</creatorcontrib><creatorcontrib>Companys, Judit</creatorcontrib><creatorcontrib>Salamanca, Patricia</creatorcontrib><creatorcontrib>Calderón-Pérez, Lorena</creatorcontrib><creatorcontrib>Pla-Pagà, Laura</creatorcontrib><creatorcontrib>Pedret, Anna</creatorcontrib><creatorcontrib>Delpino-Rius, Antoni</creatorcontrib><creatorcontrib>Herrero, Pol</creatorcontrib><creatorcontrib>Samarra, Iris</creatorcontrib><creatorcontrib>Arola, Lluís</creatorcontrib><creatorcontrib>Solà, Rosa</creatorcontrib><creatorcontrib>Del Bas, Josep M</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Physical Education Index</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>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>Coronavirus Research Database</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nutrients</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Crescenti, Anna</au><au>Caimari, Antoni</au><au>Alcaide-Hidalgo, Juan María</au><au>Mariné-Casadó, Roger</au><au>Valls, Rosa M</au><au>Companys, Judit</au><au>Salamanca, Patricia</au><au>Calderón-Pérez, Lorena</au><au>Pla-Pagà, Laura</au><au>Pedret, Anna</au><au>Delpino-Rius, Antoni</au><au>Herrero, Pol</au><au>Samarra, Iris</au><au>Arola, Lluís</au><au>Solà, Rosa</au><au>Del Bas, Josep M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hesperidin Bioavailability Is Increased by the Presence of 2S-Diastereoisomer and Micronization—A Randomized, Crossover and Double-Blind Clinical Trial</atitle><jtitle>Nutrients</jtitle><date>2022-06-01</date><risdate>2022</risdate><volume>14</volume><issue>12</issue><spage>2481</spage><pages>2481-</pages><issn>2072-6643</issn><eissn>2072-6643</eissn><abstract>Hesperidin is a flavanone abundantly found in citrus fruits for which health beneficial effects have been reported. However, hesperidin shows a low bioavailability among individuals. The aim of this study was to evaluate the effects of the micronization process and 2R- and 2S-hesperidin diastereoisomers ratio on hesperidin bioavailability. In a first phase, thirty healthy individuals consumed 500 mL of orange juice with 345 mg of hesperidin, and the levels of hesperidin metabolites excreted in urine were determined. In the second phase, fifteen individuals with intermediate hesperidin metabolite levels excreted in urine were randomized in a crossover, postprandial and double-blind intervention study. Participants consumed 500 mg of the hesperidin-supplemented Hesperidin epimeric mixture (HEM), the micronized Hesperidin epimeric mixture (MHEM) and micronized 2S-Hesperidin (M2SH) in each study visit with 1 week of washout. Hesperidin metabolites and catabolites were determined in blood and urine obtained at different timepoints over a 24 h period. The bioavailability—relative urinary hesperidin excretion (% of hesperidin ingested)—of M2SH (70 ± 14%) formed mainly by 2S-diastereoisomer was significantly higher than the bioavailability of the MHEM (55 ± 15%) and HEM (43 ± 8.0%), which consisted of a mixture of both hesperidin diastereoisomers. Relative urinary excretion of hesperidin metabolites for MHEM (9.2 ± 1.6%) was significantly higher compared to the HEM (5.2 ± 0.81%) and M2SH (3.6 ± 1.0%). In conclusion, the bioavailability of 2S-hesperidin extract was higher compared to the standard mixture of 2S-/2R-hesperidin extract due to a greater formation of hesperidin catabolites. 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subjects | Acids Bioavailability Catabolites Citrus Citrus fruits Clinical trials Colon Diastereoisomers Diastereomers Double-blind studies Excretion Flavonoids Food research Fruit juices Hesperidin Intervention Metabolites Microbiota Mixtures Nutritional aspects Particle size Urine |
title | Hesperidin Bioavailability Is Increased by the Presence of 2S-Diastereoisomer and Micronization—A Randomized, Crossover and Double-Blind Clinical Trial |
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