Bioavailability of 2- O -α- d -glucopyranosyl- l -ascorbic acid as ascorbic acid in healthy humans

Abstract Objective 2- O -α- d -glucopyranosyl-L-ascorbic acid (AA2G) is a stable glycoside, but its conversion to bioavailable ascorbic acid (AsA) in humans remains unknown. The aim of this study was to clarify that AA2G is hydrolyzed by human intestinal maltase and AA2G by oral ingestion is physiol...

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Veröffentlicht in:Nutrition (Burbank, Los Angeles County, Calif.) Los Angeles County, Calif.), 2009-06, Vol.25 (6), p.686-691
Hauptverfasser: Nakamura, Sadako, Ph.D, Oku, Tsuneyuki, Ph.D
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Oku, Tsuneyuki, Ph.D
description Abstract Objective 2- O -α- d -glucopyranosyl-L-ascorbic acid (AA2G) is a stable glycoside, but its conversion to bioavailable ascorbic acid (AsA) in humans remains unknown. The aim of this study was to clarify that AA2G is hydrolyzed by human intestinal maltase and AA2G by oral ingestion is physiologically utilized the same as AsA in human subjects. Methods The hydrolyzing activities to AA2G by human or rat intestinal homogenates were measured by high-performance liquid chromatography. In a human experiment eight healthy female subjects (23.5 ± 0.5 y old, body mass index 20.1 ± 0.7 kg/m2 ) ingested 3.84 g of AA2G (equivalent to 2 g of AsA) and 2 g of AsA. Blood was collected 0, 1, 2, 3, and 4 h after ingestion. The concentrations of serum AsA were compared with those of rats administered 76.8 mg of AA2G (equivalent to 40 mg of AsA). Results AA2G was hydrolyzed by maltase using human intestinal homogenate the same as that of rat. When AA2G was orally administered to human subjects, the changed value of the serum concentration of AsA was 1.6 mg/100 mL from baseline at 2 h and then maintained until 4 h after administration. These concentrations were not significantly different from those after ingestion of AsA. In the case of rat, the AsA concentrations in serum were linearly increased to 1.7 mg/100 mL until 3 h after administration. Conclusion AA2G is hydrolyzed by intestinal maltase and acts as AsA in humans. The present results will contribute to the development of functional food with health claims to supply AsA.
doi_str_mv 10.1016/j.nut.2008.11.031
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The aim of this study was to clarify that AA2G is hydrolyzed by human intestinal maltase and AA2G by oral ingestion is physiologically utilized the same as AsA in human subjects. Methods The hydrolyzing activities to AA2G by human or rat intestinal homogenates were measured by high-performance liquid chromatography. In a human experiment eight healthy female subjects (23.5 ± 0.5 y old, body mass index 20.1 ± 0.7 kg/m2 ) ingested 3.84 g of AA2G (equivalent to 2 g of AsA) and 2 g of AsA. Blood was collected 0, 1, 2, 3, and 4 h after ingestion. The concentrations of serum AsA were compared with those of rats administered 76.8 mg of AA2G (equivalent to 40 mg of AsA). Results AA2G was hydrolyzed by maltase using human intestinal homogenate the same as that of rat. When AA2G was orally administered to human subjects, the changed value of the serum concentration of AsA was 1.6 mg/100 mL from baseline at 2 h and then maintained until 4 h after administration. These concentrations were not significantly different from those after ingestion of AsA. In the case of rat, the AsA concentrations in serum were linearly increased to 1.7 mg/100 mL until 3 h after administration. Conclusion AA2G is hydrolyzed by intestinal maltase and acts as AsA in humans. The present results will contribute to the development of functional food with health claims to supply AsA.</description><identifier>ISSN: 0899-9007</identifier><identifier>EISSN: 1873-1244</identifier><identifier>DOI: 10.1016/j.nut.2008.11.031</identifier><identifier>PMID: 19230615</identifier><identifier>CODEN: NUTRER</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>2- O-α- d-glucopyranosyl-L-ascorbic acid ; AA2G ; administered dose ; alpha-glucosidase ; alpha-Glucosidases - metabolism ; animal models ; Animals ; Area Under Curve ; Ascorbic acid ; Ascorbic Acid - analogs &amp; derivatives ; Ascorbic Acid - pharmacokinetics ; Bioavailability in humans ; Biological and medical sciences ; Biological Availability ; blood serum ; Chromatography, High Pressure Liquid ; dose response ; Feeding. Feeding behavior ; Female ; Fundamental and applied biological sciences. Psychology ; Gastroenterology and Hepatology ; glycosides ; health foods ; Humans ; Hydrolysis ; intestinal absorption ; Intestinal maltase ; Intestinal Mucosa - enzymology ; nutrient availability ; Rats ; Species Specificity ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; vitamin metabolism ; vitamin supplements ; women ; Young Adult</subject><ispartof>Nutrition (Burbank, Los Angeles County, Calif.), 2009-06, Vol.25 (6), p.686-691</ispartof><rights>Elsevier Inc.</rights><rights>2009 Elsevier Inc.</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c460t-71929cc1b14b070c43e46a53c4d10217a9e57044c09d7d09b66508a1428807aa3</citedby><cites>FETCH-LOGICAL-c460t-71929cc1b14b070c43e46a53c4d10217a9e57044c09d7d09b66508a1428807aa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0899900708005352$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,64363,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=21419795$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19230615$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nakamura, Sadako, Ph.D</creatorcontrib><creatorcontrib>Oku, Tsuneyuki, Ph.D</creatorcontrib><title>Bioavailability of 2- O -α- d -glucopyranosyl- l -ascorbic acid as ascorbic acid in healthy humans</title><title>Nutrition (Burbank, Los Angeles County, Calif.)</title><addtitle>Nutrition</addtitle><description>Abstract Objective 2- O -α- d -glucopyranosyl-L-ascorbic acid (AA2G) is a stable glycoside, but its conversion to bioavailable ascorbic acid (AsA) in humans remains unknown. The aim of this study was to clarify that AA2G is hydrolyzed by human intestinal maltase and AA2G by oral ingestion is physiologically utilized the same as AsA in human subjects. Methods The hydrolyzing activities to AA2G by human or rat intestinal homogenates were measured by high-performance liquid chromatography. In a human experiment eight healthy female subjects (23.5 ± 0.5 y old, body mass index 20.1 ± 0.7 kg/m2 ) ingested 3.84 g of AA2G (equivalent to 2 g of AsA) and 2 g of AsA. Blood was collected 0, 1, 2, 3, and 4 h after ingestion. The concentrations of serum AsA were compared with those of rats administered 76.8 mg of AA2G (equivalent to 40 mg of AsA). Results AA2G was hydrolyzed by maltase using human intestinal homogenate the same as that of rat. When AA2G was orally administered to human subjects, the changed value of the serum concentration of AsA was 1.6 mg/100 mL from baseline at 2 h and then maintained until 4 h after administration. These concentrations were not significantly different from those after ingestion of AsA. In the case of rat, the AsA concentrations in serum were linearly increased to 1.7 mg/100 mL until 3 h after administration. Conclusion AA2G is hydrolyzed by intestinal maltase and acts as AsA in humans. The present results will contribute to the development of functional food with health claims to supply AsA.</description><subject>2- O-α- d-glucopyranosyl-L-ascorbic acid</subject><subject>AA2G</subject><subject>administered dose</subject><subject>alpha-glucosidase</subject><subject>alpha-Glucosidases - metabolism</subject><subject>animal models</subject><subject>Animals</subject><subject>Area Under Curve</subject><subject>Ascorbic acid</subject><subject>Ascorbic Acid - analogs &amp; derivatives</subject><subject>Ascorbic Acid - pharmacokinetics</subject><subject>Bioavailability in humans</subject><subject>Biological and medical sciences</subject><subject>Biological Availability</subject><subject>blood serum</subject><subject>Chromatography, High Pressure Liquid</subject><subject>dose response</subject><subject>Feeding. Feeding behavior</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gastroenterology and Hepatology</subject><subject>glycosides</subject><subject>health foods</subject><subject>Humans</subject><subject>Hydrolysis</subject><subject>intestinal absorption</subject><subject>Intestinal maltase</subject><subject>Intestinal Mucosa - enzymology</subject><subject>nutrient availability</subject><subject>Rats</subject><subject>Species Specificity</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>vitamin metabolism</subject><subject>vitamin supplements</subject><subject>women</subject><subject>Young Adult</subject><issn>0899-9007</issn><issn>1873-1244</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9ks2KFDEQx4Mo7rj6AF40F72lrUqnP4KwoItfsLCHdc8hnU7vZMx0xqR7oR_LF_GZTDODogdPgfCrfxW_KkKeIxQIWL_ZFeM8FRygLRALKPEB2WDblAy5EA_JBlopmQRozsiTlHYAgLKWj8kZSl5CjdWGmPcu6HvtvO6cd9NCw0A5o9eU_fzBaE_ZnZ9NOCxRjyEtnlFPmU4mxM4Zqo3rqU707w830q3VftoudDvv9ZiekkeD9sk-O73n5Pbjh6-Xn9nV9acvl--umBE1TKzJU0ljsEPRQQNGlFbUuiqN6BE4NlraqgEhDMi-6UF2dV1Bq1HwtoVG6_KcvD7mHmL4Pts0qb1LxnqvRxvmpOrcQeagDOIRNDGkFO2gDtHtdVwUglrNqp3KZtVqViGqbDbXvDiFz93e9n8qTioz8OoEZB3aD9mYcek3x1GgbOTKvTxygw5K38XM3N5wwDL35U0r20y8PRI2y7p3NqpknB2N7V20ZlJ9cP8d9OKfauPd6PJI3-xi0y7MccxbUKgSV6Bu1iNZbwRagKqsePkLhM-yMw</recordid><startdate>20090601</startdate><enddate>20090601</enddate><creator>Nakamura, Sadako, Ph.D</creator><creator>Oku, Tsuneyuki, Ph.D</creator><general>Elsevier Inc</general><general>[New York]: Elsevier Science Inc</general><general>Elsevier</general><scope>FBQ</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>7X8</scope></search><sort><creationdate>20090601</creationdate><title>Bioavailability of 2- O -α- d -glucopyranosyl- l -ascorbic acid as ascorbic acid in healthy humans</title><author>Nakamura, Sadako, Ph.D ; Oku, Tsuneyuki, Ph.D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c460t-71929cc1b14b070c43e46a53c4d10217a9e57044c09d7d09b66508a1428807aa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>2- O-α- d-glucopyranosyl-L-ascorbic acid</topic><topic>AA2G</topic><topic>administered dose</topic><topic>alpha-glucosidase</topic><topic>alpha-Glucosidases - metabolism</topic><topic>animal models</topic><topic>Animals</topic><topic>Area Under Curve</topic><topic>Ascorbic acid</topic><topic>Ascorbic Acid - analogs &amp; derivatives</topic><topic>Ascorbic Acid - pharmacokinetics</topic><topic>Bioavailability in humans</topic><topic>Biological and medical sciences</topic><topic>Biological Availability</topic><topic>blood serum</topic><topic>Chromatography, High Pressure Liquid</topic><topic>dose response</topic><topic>Feeding. Feeding behavior</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gastroenterology and Hepatology</topic><topic>glycosides</topic><topic>health foods</topic><topic>Humans</topic><topic>Hydrolysis</topic><topic>intestinal absorption</topic><topic>Intestinal maltase</topic><topic>Intestinal Mucosa - enzymology</topic><topic>nutrient availability</topic><topic>Rats</topic><topic>Species Specificity</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>vitamin metabolism</topic><topic>vitamin supplements</topic><topic>women</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nakamura, Sadako, Ph.D</creatorcontrib><creatorcontrib>Oku, Tsuneyuki, Ph.D</creatorcontrib><collection>AGRIS</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>MEDLINE - Academic</collection><jtitle>Nutrition (Burbank, Los Angeles County, Calif.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nakamura, Sadako, Ph.D</au><au>Oku, Tsuneyuki, Ph.D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bioavailability of 2- O -α- d -glucopyranosyl- l -ascorbic acid as ascorbic acid in healthy humans</atitle><jtitle>Nutrition (Burbank, Los Angeles County, Calif.)</jtitle><addtitle>Nutrition</addtitle><date>2009-06-01</date><risdate>2009</risdate><volume>25</volume><issue>6</issue><spage>686</spage><epage>691</epage><pages>686-691</pages><issn>0899-9007</issn><eissn>1873-1244</eissn><coden>NUTRER</coden><abstract>Abstract Objective 2- O -α- d -glucopyranosyl-L-ascorbic acid (AA2G) is a stable glycoside, but its conversion to bioavailable ascorbic acid (AsA) in humans remains unknown. The aim of this study was to clarify that AA2G is hydrolyzed by human intestinal maltase and AA2G by oral ingestion is physiologically utilized the same as AsA in human subjects. Methods The hydrolyzing activities to AA2G by human or rat intestinal homogenates were measured by high-performance liquid chromatography. In a human experiment eight healthy female subjects (23.5 ± 0.5 y old, body mass index 20.1 ± 0.7 kg/m2 ) ingested 3.84 g of AA2G (equivalent to 2 g of AsA) and 2 g of AsA. Blood was collected 0, 1, 2, 3, and 4 h after ingestion. The concentrations of serum AsA were compared with those of rats administered 76.8 mg of AA2G (equivalent to 40 mg of AsA). Results AA2G was hydrolyzed by maltase using human intestinal homogenate the same as that of rat. When AA2G was orally administered to human subjects, the changed value of the serum concentration of AsA was 1.6 mg/100 mL from baseline at 2 h and then maintained until 4 h after administration. These concentrations were not significantly different from those after ingestion of AsA. In the case of rat, the AsA concentrations in serum were linearly increased to 1.7 mg/100 mL until 3 h after administration. Conclusion AA2G is hydrolyzed by intestinal maltase and acts as AsA in humans. The present results will contribute to the development of functional food with health claims to supply AsA.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>19230615</pmid><doi>10.1016/j.nut.2008.11.031</doi><tpages>6</tpages></addata></record>
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identifier ISSN: 0899-9007
ispartof Nutrition (Burbank, Los Angeles County, Calif.), 2009-06, Vol.25 (6), p.686-691
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source MEDLINE; Elsevier ScienceDirect Journals; ProQuest Central UK/Ireland
subjects 2- O-α- d-glucopyranosyl-L-ascorbic acid
AA2G
administered dose
alpha-glucosidase
alpha-Glucosidases - metabolism
animal models
Animals
Area Under Curve
Ascorbic acid
Ascorbic Acid - analogs & derivatives
Ascorbic Acid - pharmacokinetics
Bioavailability in humans
Biological and medical sciences
Biological Availability
blood serum
Chromatography, High Pressure Liquid
dose response
Feeding. Feeding behavior
Female
Fundamental and applied biological sciences. Psychology
Gastroenterology and Hepatology
glycosides
health foods
Humans
Hydrolysis
intestinal absorption
Intestinal maltase
Intestinal Mucosa - enzymology
nutrient availability
Rats
Species Specificity
Vertebrates: anatomy and physiology, studies on body, several organs or systems
vitamin metabolism
vitamin supplements
women
Young Adult
title Bioavailability of 2- O -α- d -glucopyranosyl- l -ascorbic acid as ascorbic acid in healthy humans
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