Fermented milk, Kefram-Kefir enhances glucose uptake into insulin-responsive muscle cells
Diminution of insulin-responses in the target organ is the primary cause of non-insulin dependent diabetes mellitus (NIDDM).It is thought to be correlated to the excessive production of reactive oxygen species (ROS). In this article, we attempted to evaluate whether fermented milk, Kefram-Kefir know...
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creator | TERUYA, Kiichiro YAMASHITA, Maiko TOMINAGA, Rumi NAGIRA, Tsutomu SHIM, Sun-Yup KATAKURA, Yoshinori TOKUMARU, Sennosuke TOKUMARU, Koichiro BARNES, David SHIRAHATAL, Sanetaka |
description | Diminution of insulin-responses in the target organ is the primary cause of non-insulin dependent diabetes mellitus (NIDDM).It is thought to be correlated to the excessive production of reactive oxygen species (ROS). In this article, we attempted to evaluate whether fermented milk, Kefram-Kefir known as an antioxidant, reduces the cellular ROS levels and can stimulate the glucose uptake in L6 skeletal muscle cells. Water-soluble or chloroform/methanol-extracted fractions from Kefram-Kefir were examined to evaluate the glucose uptake ability of L6 myotubes.As a result, the water-soluble fraction augmented the uptake of glucose in L6 myotubes both in the presence and absence of insulin stimulation. Estimation of intracellular ROS level revealed that the water-soluble fraction of Kefram-Kefir reduced the intracellular ROS level on both the undifferentiated and differentiated L6 cells. Especially, glucose uptake was augmented up to six times with the addition of water-soluble fraction in the insulin-stimulated L6 myotubes. Glucose transport determination revealed that the active agent in Kefram-Kefir was resistant to autoclave and stable in pH range from 4 to 10, and the small molecule below the molecular weight of 1000. Furthermore, this augmentation was inhibited in the presence of phosphatidylinositol 3-kinase (PI 3-kinase) inhibitor wortmannin. Considering together with the reports that PI 3-kinase is locatedin the insulin signaling pathway and the participation in the translocation of glucose transporter 4 to the cell membrane, it is suggested that the water-soluble fraction of Kefram-Kefir activates PI 3-kinase or other upstream molecules in the insulin signaling pathway, which resulted in the augmentation of glucose uptake and its specific inhibition by wortmannin. |
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In this article, we attempted to evaluate whether fermented milk, Kefram-Kefir known as an antioxidant, reduces the cellular ROS levels and can stimulate the glucose uptake in L6 skeletal muscle cells. Water-soluble or chloroform/methanol-extracted fractions from Kefram-Kefir were examined to evaluate the glucose uptake ability of L6 myotubes.As a result, the water-soluble fraction augmented the uptake of glucose in L6 myotubes both in the presence and absence of insulin stimulation. Estimation of intracellular ROS level revealed that the water-soluble fraction of Kefram-Kefir reduced the intracellular ROS level on both the undifferentiated and differentiated L6 cells. Especially, glucose uptake was augmented up to six times with the addition of water-soluble fraction in the insulin-stimulated L6 myotubes. Glucose transport determination revealed that the active agent in Kefram-Kefir was resistant to autoclave and stable in pH range from 4 to 10, and the small molecule below the molecular weight of 1000. Furthermore, this augmentation was inhibited in the presence of phosphatidylinositol 3-kinase (PI 3-kinase) inhibitor wortmannin. Considering together with the reports that PI 3-kinase is locatedin the insulin signaling pathway and the participation in the translocation of glucose transporter 4 to the cell membrane, it is suggested that the water-soluble fraction of Kefram-Kefir activates PI 3-kinase or other upstream molecules in the insulin signaling pathway, which resulted in the augmentation of glucose uptake and its specific inhibition by wortmannin.</description><identifier>ISSN: 0920-9069</identifier><identifier>EISSN: 1573-0778</identifier><identifier>DOI: 10.1023/A:1023926407877</identifier><identifier>PMID: 19003111</identifier><language>eng</language><publisher>Dordrecht: Springer</publisher><subject>1-Phosphatidylinositol 3-kinase ; Biological and medical sciences ; Cell differentiation ; Cell membranes ; Chloroform ; Diabetes mellitus (insulin dependent) ; Diabetes mellitus (non-insulin dependent) ; Fermented milk products ; Fundamental and applied biological sciences. Psychology ; Glucose ; Glucose transport ; Glucose transporter ; Insulin ; Intracellular ; Kefir ; Molecular weight ; Myotubes ; Reactive oxygen species ; Signal transduction ; Skeletal muscle ; Wortmannin</subject><ispartof>Cytotechnology (Dordrecht), 2002-11, Vol.40 (1-3), p.107-116</ispartof><rights>2003 INIST-CNRS</rights><rights>Kluwer Academic Publishers 2002.</rights><rights>Kluwer Academic Publishers 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-29408974df50db4cf38c075f28a7ea3d0a839f67e29912c96367d4312e9eeb5e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3449522/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2918256434?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>230,309,310,314,723,776,780,785,786,881,21368,23910,23911,25119,27903,27904,33723,33724,43784,53769,53771,64361,64363,64365,72215</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14917384$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19003111$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TERUYA, Kiichiro</creatorcontrib><creatorcontrib>YAMASHITA, Maiko</creatorcontrib><creatorcontrib>TOMINAGA, Rumi</creatorcontrib><creatorcontrib>NAGIRA, Tsutomu</creatorcontrib><creatorcontrib>SHIM, Sun-Yup</creatorcontrib><creatorcontrib>KATAKURA, Yoshinori</creatorcontrib><creatorcontrib>TOKUMARU, Sennosuke</creatorcontrib><creatorcontrib>TOKUMARU, Koichiro</creatorcontrib><creatorcontrib>BARNES, David</creatorcontrib><creatorcontrib>SHIRAHATAL, Sanetaka</creatorcontrib><title>Fermented milk, Kefram-Kefir enhances glucose uptake into insulin-responsive muscle cells</title><title>Cytotechnology (Dordrecht)</title><addtitle>Cytotechnology</addtitle><description>Diminution of insulin-responses in the target organ is the primary cause of non-insulin dependent diabetes mellitus (NIDDM).It is thought to be correlated to the excessive production of reactive oxygen species (ROS). In this article, we attempted to evaluate whether fermented milk, Kefram-Kefir known as an antioxidant, reduces the cellular ROS levels and can stimulate the glucose uptake in L6 skeletal muscle cells. Water-soluble or chloroform/methanol-extracted fractions from Kefram-Kefir were examined to evaluate the glucose uptake ability of L6 myotubes.As a result, the water-soluble fraction augmented the uptake of glucose in L6 myotubes both in the presence and absence of insulin stimulation. Estimation of intracellular ROS level revealed that the water-soluble fraction of Kefram-Kefir reduced the intracellular ROS level on both the undifferentiated and differentiated L6 cells. Especially, glucose uptake was augmented up to six times with the addition of water-soluble fraction in the insulin-stimulated L6 myotubes. Glucose transport determination revealed that the active agent in Kefram-Kefir was resistant to autoclave and stable in pH range from 4 to 10, and the small molecule below the molecular weight of 1000. Furthermore, this augmentation was inhibited in the presence of phosphatidylinositol 3-kinase (PI 3-kinase) inhibitor wortmannin. Considering together with the reports that PI 3-kinase is locatedin the insulin signaling pathway and the participation in the translocation of glucose transporter 4 to the cell membrane, it is suggested that the water-soluble fraction of Kefram-Kefir activates PI 3-kinase or other upstream molecules in the insulin signaling pathway, which resulted in the augmentation of glucose uptake and its specific inhibition by wortmannin.</description><subject>1-Phosphatidylinositol 3-kinase</subject><subject>Biological and medical sciences</subject><subject>Cell differentiation</subject><subject>Cell membranes</subject><subject>Chloroform</subject><subject>Diabetes mellitus (insulin dependent)</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Fermented milk products</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glucose</subject><subject>Glucose transport</subject><subject>Glucose transporter</subject><subject>Insulin</subject><subject>Intracellular</subject><subject>Kefir</subject><subject>Molecular weight</subject><subject>Myotubes</subject><subject>Reactive oxygen species</subject><subject>Signal transduction</subject><subject>Skeletal muscle</subject><subject>Wortmannin</subject><issn>0920-9069</issn><issn>1573-0778</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kcFPFTEQxhujgQdy5mY2MerFxbbT3XY8mBAiaiDxogdOm77uLBS63We7S-J_T4lPFA9e5jvML1--mY-xQ8GPBJfw7vj9vaBsFddG6ydsJRoNNdfaPGUrjpLXyFvcZXs5X3POUQvYYbsCOQchxIpdnFIaKc7UV6MPN2-rMxqSHesiPlUUr2x0lKvLsLgpU7VsZntDlY_zVEZego91oryZYva3VI1LdoEqRyHk5-zZYEOmg63us--nH7-dfK7Pv376cnJ8XjsFONcSFTeoVT80vF8rN4BxXDeDNFaThZ5bAzi0miSikA5baHWvQEhConVDsM8-_PLdLOuReleOSTZ0m-RHm352k_Xd4030V93ldNuBUthIWQzebA3S9GOhPHejz_cn2EjTkjsNYLREgEK-_i8pSgUlYFPAl_-A19OSYnlDJ1EY2bQKVKFe_J38IfLvdgrwagvY7GwoxUTn8x9OodBgFNwBTlaeuQ</recordid><startdate>20021101</startdate><enddate>20021101</enddate><creator>TERUYA, Kiichiro</creator><creator>YAMASHITA, Maiko</creator><creator>TOMINAGA, Rumi</creator><creator>NAGIRA, Tsutomu</creator><creator>SHIM, Sun-Yup</creator><creator>KATAKURA, Yoshinori</creator><creator>TOKUMARU, Sennosuke</creator><creator>TOKUMARU, Koichiro</creator><creator>BARNES, David</creator><creator>SHIRAHATAL, Sanetaka</creator><general>Springer</general><general>Springer Nature B.V</general><general>Kluwer Academic Publishers</general><scope>IQODW</scope><scope>NPM</scope><scope>8FE</scope><scope>8FH</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20021101</creationdate><title>Fermented milk, Kefram-Kefir enhances glucose uptake into insulin-responsive muscle cells</title><author>TERUYA, Kiichiro ; YAMASHITA, Maiko ; TOMINAGA, Rumi ; NAGIRA, Tsutomu ; SHIM, Sun-Yup ; KATAKURA, Yoshinori ; TOKUMARU, Sennosuke ; TOKUMARU, Koichiro ; BARNES, David ; SHIRAHATAL, Sanetaka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-29408974df50db4cf38c075f28a7ea3d0a839f67e29912c96367d4312e9eeb5e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>1-Phosphatidylinositol 3-kinase</topic><topic>Biological and medical sciences</topic><topic>Cell differentiation</topic><topic>Cell membranes</topic><topic>Chloroform</topic><topic>Diabetes mellitus (insulin dependent)</topic><topic>Diabetes mellitus (non-insulin dependent)</topic><topic>Fermented milk products</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glucose</topic><topic>Glucose transport</topic><topic>Glucose transporter</topic><topic>Insulin</topic><topic>Intracellular</topic><topic>Kefir</topic><topic>Molecular weight</topic><topic>Myotubes</topic><topic>Reactive oxygen species</topic><topic>Signal transduction</topic><topic>Skeletal muscle</topic><topic>Wortmannin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TERUYA, Kiichiro</creatorcontrib><creatorcontrib>YAMASHITA, Maiko</creatorcontrib><creatorcontrib>TOMINAGA, Rumi</creatorcontrib><creatorcontrib>NAGIRA, Tsutomu</creatorcontrib><creatorcontrib>SHIM, Sun-Yup</creatorcontrib><creatorcontrib>KATAKURA, Yoshinori</creatorcontrib><creatorcontrib>TOKUMARU, Sennosuke</creatorcontrib><creatorcontrib>TOKUMARU, Koichiro</creatorcontrib><creatorcontrib>BARNES, David</creatorcontrib><creatorcontrib>SHIRAHATAL, Sanetaka</creatorcontrib><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science 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>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cytotechnology (Dordrecht)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TERUYA, Kiichiro</au><au>YAMASHITA, Maiko</au><au>TOMINAGA, Rumi</au><au>NAGIRA, Tsutomu</au><au>SHIM, Sun-Yup</au><au>KATAKURA, Yoshinori</au><au>TOKUMARU, Sennosuke</au><au>TOKUMARU, Koichiro</au><au>BARNES, David</au><au>SHIRAHATAL, Sanetaka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fermented milk, Kefram-Kefir enhances glucose uptake into insulin-responsive muscle cells</atitle><jtitle>Cytotechnology (Dordrecht)</jtitle><addtitle>Cytotechnology</addtitle><date>2002-11-01</date><risdate>2002</risdate><volume>40</volume><issue>1-3</issue><spage>107</spage><epage>116</epage><pages>107-116</pages><issn>0920-9069</issn><eissn>1573-0778</eissn><abstract>Diminution of insulin-responses in the target organ is the primary cause of non-insulin dependent diabetes mellitus (NIDDM).It is thought to be correlated to the excessive production of reactive oxygen species (ROS). In this article, we attempted to evaluate whether fermented milk, Kefram-Kefir known as an antioxidant, reduces the cellular ROS levels and can stimulate the glucose uptake in L6 skeletal muscle cells. Water-soluble or chloroform/methanol-extracted fractions from Kefram-Kefir were examined to evaluate the glucose uptake ability of L6 myotubes.As a result, the water-soluble fraction augmented the uptake of glucose in L6 myotubes both in the presence and absence of insulin stimulation. Estimation of intracellular ROS level revealed that the water-soluble fraction of Kefram-Kefir reduced the intracellular ROS level on both the undifferentiated and differentiated L6 cells. Especially, glucose uptake was augmented up to six times with the addition of water-soluble fraction in the insulin-stimulated L6 myotubes. Glucose transport determination revealed that the active agent in Kefram-Kefir was resistant to autoclave and stable in pH range from 4 to 10, and the small molecule below the molecular weight of 1000. Furthermore, this augmentation was inhibited in the presence of phosphatidylinositol 3-kinase (PI 3-kinase) inhibitor wortmannin. Considering together with the reports that PI 3-kinase is locatedin the insulin signaling pathway and the participation in the translocation of glucose transporter 4 to the cell membrane, it is suggested that the water-soluble fraction of Kefram-Kefir activates PI 3-kinase or other upstream molecules in the insulin signaling pathway, which resulted in the augmentation of glucose uptake and its specific inhibition by wortmannin.</abstract><cop>Dordrecht</cop><pub>Springer</pub><pmid>19003111</pmid><doi>10.1023/A:1023926407877</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 1-Phosphatidylinositol 3-kinase Biological and medical sciences Cell differentiation Cell membranes Chloroform Diabetes mellitus (insulin dependent) Diabetes mellitus (non-insulin dependent) Fermented milk products Fundamental and applied biological sciences. Psychology Glucose Glucose transport Glucose transporter Insulin Intracellular Kefir Molecular weight Myotubes Reactive oxygen species Signal transduction Skeletal muscle Wortmannin |
title | Fermented milk, Kefram-Kefir enhances glucose uptake into insulin-responsive muscle cells |
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