Inhibitory mechanism of caffeine on insulin-stimulated glucose uptake in adipose cells
Caffeine inhibits insulin-induced glucose uptake in rat adipocytes and also decreases insulin sensitivity, including whole-body glucose disposal and glucose uptake in skeletal muscle, during a euglycemic–hyperinsulinemic clamp in human. However, the mechanism by which caffeine decreases the insulin...
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Veröffentlicht in: | Biochemical pharmacology 2004-11, Vol.68 (10), p.1929-1937 |
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container_end_page | 1937 |
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container_issue | 10 |
container_start_page | 1929 |
container_title | Biochemical pharmacology |
container_volume | 68 |
creator | Akiba, Tetsuo Yaguchi, Kuniko Tsutsumi, Kikue Nishioka, Tatsuo Koyama, Ichiko Nomura, Masaaki Yokogawa, Koichi Moritani, Shuzo Miyamoto, Ken-ichi |
description | Caffeine inhibits insulin-induced glucose uptake in rat adipocytes and also decreases insulin sensitivity, including whole-body glucose disposal and glucose uptake in skeletal muscle, during a euglycemic–hyperinsulinemic clamp in human. However, the mechanism by which caffeine decreases the insulin sensitivity is not still clear. We found that pre-treatment with caffeine inhibited the insulin-induced 2-deoxy-
d-[1-
3H]glucose uptake in a concentration-dependent manner in mouse preadipose MC-3T3-G2/PA6 cells differentiated into mature adipose cells. Caffeine also suppressed insulin-induced GLUT4 translocation in the differentiated cells. Although caffeine did not alter insulin-induced activation of PI3K and protein kinase C-zeta (PKCζ), an isoform of atypical PKC, which is reported to have an important role in insulin-induced GLUT4 translocation, we found that insulin-induced phosphorylation and activation of Akt were blocked by pre-treatment with caffeine. Inhibition of insulin-induced 2-deoxy-
d-[1-
3H]glucose uptake by caffeine was also observed in primary cultured brown adipocytes in a concentration-dependent manner. These results may, in part, explain the ability of caffeine to decrease insulin sensitivity. |
doi_str_mv | 10.1016/j.bcp.2004.07.036 |
format | Article |
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d-[1-
3H]glucose uptake in a concentration-dependent manner in mouse preadipose MC-3T3-G2/PA6 cells differentiated into mature adipose cells. Caffeine also suppressed insulin-induced GLUT4 translocation in the differentiated cells. Although caffeine did not alter insulin-induced activation of PI3K and protein kinase C-zeta (PKCζ), an isoform of atypical PKC, which is reported to have an important role in insulin-induced GLUT4 translocation, we found that insulin-induced phosphorylation and activation of Akt were blocked by pre-treatment with caffeine. Inhibition of insulin-induced 2-deoxy-
d-[1-
3H]glucose uptake by caffeine was also observed in primary cultured brown adipocytes in a concentration-dependent manner. These results may, in part, explain the ability of caffeine to decrease insulin sensitivity.</description><identifier>ISSN: 0006-2952</identifier><identifier>EISSN: 1873-2968</identifier><identifier>DOI: 10.1016/j.bcp.2004.07.036</identifier><identifier>PMID: 15476664</identifier><identifier>CODEN: BCPCA6</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adipocytes ; Adipocytes - drug effects ; Adipocytes - metabolism ; Akt ; Animals ; Biological and medical sciences ; Biological Transport ; Caffeine - pharmacology ; Cells, Cultured ; Cyclic AMP - metabolism ; Deoxyglucose - metabolism ; General and cellular metabolism. Vitamins ; Glucose - metabolism ; Glucose uptake ; GLUT4 ; Insulin ; Insulin - pharmacology ; Medical sciences ; Mice ; Mice, Inbred C57BL ; Pharmacology. Drug treatments ; Phosphatidylinositol 3-kinase ; Phosphatidylinositol 3-Kinases - metabolism ; Protein Kinase C - metabolism ; Protein-Serine-Threonine Kinases - metabolism ; Proto-Oncogene Proteins - metabolism ; Proto-Oncogene Proteins c-akt ; Receptors, Purinergic P1 - metabolism ; Tritium</subject><ispartof>Biochemical pharmacology, 2004-11, Vol.68 (10), p.1929-1937</ispartof><rights>2004 Elsevier Inc.</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c445t-f75e579b55a7dfd77a68c8820918cd000095db26878d4cf57118ed951f11b4973</citedby><cites>FETCH-LOGICAL-c445t-f75e579b55a7dfd77a68c8820918cd000095db26878d4cf57118ed951f11b4973</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bcp.2004.07.036$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16197391$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15476664$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Akiba, Tetsuo</creatorcontrib><creatorcontrib>Yaguchi, Kuniko</creatorcontrib><creatorcontrib>Tsutsumi, Kikue</creatorcontrib><creatorcontrib>Nishioka, Tatsuo</creatorcontrib><creatorcontrib>Koyama, Ichiko</creatorcontrib><creatorcontrib>Nomura, Masaaki</creatorcontrib><creatorcontrib>Yokogawa, Koichi</creatorcontrib><creatorcontrib>Moritani, Shuzo</creatorcontrib><creatorcontrib>Miyamoto, Ken-ichi</creatorcontrib><title>Inhibitory mechanism of caffeine on insulin-stimulated glucose uptake in adipose cells</title><title>Biochemical pharmacology</title><addtitle>Biochem Pharmacol</addtitle><description>Caffeine inhibits insulin-induced glucose uptake in rat adipocytes and also decreases insulin sensitivity, including whole-body glucose disposal and glucose uptake in skeletal muscle, during a euglycemic–hyperinsulinemic clamp in human. However, the mechanism by which caffeine decreases the insulin sensitivity is not still clear. We found that pre-treatment with caffeine inhibited the insulin-induced 2-deoxy-
d-[1-
3H]glucose uptake in a concentration-dependent manner in mouse preadipose MC-3T3-G2/PA6 cells differentiated into mature adipose cells. Caffeine also suppressed insulin-induced GLUT4 translocation in the differentiated cells. Although caffeine did not alter insulin-induced activation of PI3K and protein kinase C-zeta (PKCζ), an isoform of atypical PKC, which is reported to have an important role in insulin-induced GLUT4 translocation, we found that insulin-induced phosphorylation and activation of Akt were blocked by pre-treatment with caffeine. Inhibition of insulin-induced 2-deoxy-
d-[1-
3H]glucose uptake by caffeine was also observed in primary cultured brown adipocytes in a concentration-dependent manner. These results may, in part, explain the ability of caffeine to decrease insulin sensitivity.</description><subject>Adipocytes</subject><subject>Adipocytes - drug effects</subject><subject>Adipocytes - metabolism</subject><subject>Akt</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biological Transport</subject><subject>Caffeine - pharmacology</subject><subject>Cells, Cultured</subject><subject>Cyclic AMP - metabolism</subject><subject>Deoxyglucose - metabolism</subject><subject>General and cellular metabolism. Vitamins</subject><subject>Glucose - metabolism</subject><subject>Glucose uptake</subject><subject>GLUT4</subject><subject>Insulin</subject><subject>Insulin - pharmacology</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Pharmacology. Drug treatments</subject><subject>Phosphatidylinositol 3-kinase</subject><subject>Phosphatidylinositol 3-Kinases - metabolism</subject><subject>Protein Kinase C - metabolism</subject><subject>Protein-Serine-Threonine Kinases - metabolism</subject><subject>Proto-Oncogene Proteins - metabolism</subject><subject>Proto-Oncogene Proteins c-akt</subject><subject>Receptors, Purinergic P1 - metabolism</subject><subject>Tritium</subject><issn>0006-2952</issn><issn>1873-2968</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtKxDAUhoMoOl4ewI10o7vWpNNciisRbyC4UbchTU6cjG1ak1aYtzdlBty5Ohe-c_j5EDonuCCYsOt10eihKDGuCswLvGR7aEEEX-ZlzcQ-WmCMWeppeYSOY1zPo2DkEB0RWnHGWLVAH89-5Ro39mGTdaBXyrvYZb3NtLIWnIes95nzcWqdz-PouqlVI5jss510HyGbhlF9QSIyZdwwbzS0bTxFB1a1Ec529QS9P9y_3T3lL6-Pz3e3L7muKjrmllOgvG4oVdxYw7liQgtR4poIbVJeXFPTlExwYSptKSdEgKkpsYQ0Vc2XJ-hq-3cI_fcEcZSdi3MC5aGfomSsZhjzZQLJFtShjzGAlUNwnQobSbCcZcq1TDLlLFNiLpPMdHOxez41HZi_i529BFzuABW1am1QXrv4xzGSItYkcTdbDpKKHwdBRu3AazAugB6l6d0_MX4BZa-R2A</recordid><startdate>20041115</startdate><enddate>20041115</enddate><creator>Akiba, Tetsuo</creator><creator>Yaguchi, Kuniko</creator><creator>Tsutsumi, Kikue</creator><creator>Nishioka, Tatsuo</creator><creator>Koyama, Ichiko</creator><creator>Nomura, Masaaki</creator><creator>Yokogawa, Koichi</creator><creator>Moritani, Shuzo</creator><creator>Miyamoto, Ken-ichi</creator><general>Elsevier Inc</general><general>Elsevier Science</general><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>20041115</creationdate><title>Inhibitory mechanism of caffeine on insulin-stimulated glucose uptake in adipose cells</title><author>Akiba, Tetsuo ; Yaguchi, Kuniko ; Tsutsumi, Kikue ; Nishioka, Tatsuo ; Koyama, Ichiko ; Nomura, Masaaki ; Yokogawa, Koichi ; Moritani, Shuzo ; Miyamoto, Ken-ichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c445t-f75e579b55a7dfd77a68c8820918cd000095db26878d4cf57118ed951f11b4973</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adipocytes</topic><topic>Adipocytes - drug effects</topic><topic>Adipocytes - metabolism</topic><topic>Akt</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biological Transport</topic><topic>Caffeine - pharmacology</topic><topic>Cells, Cultured</topic><topic>Cyclic AMP - metabolism</topic><topic>Deoxyglucose - metabolism</topic><topic>General and cellular metabolism. Vitamins</topic><topic>Glucose - metabolism</topic><topic>Glucose uptake</topic><topic>GLUT4</topic><topic>Insulin</topic><topic>Insulin - pharmacology</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Pharmacology. Drug treatments</topic><topic>Phosphatidylinositol 3-kinase</topic><topic>Phosphatidylinositol 3-Kinases - metabolism</topic><topic>Protein Kinase C - metabolism</topic><topic>Protein-Serine-Threonine Kinases - metabolism</topic><topic>Proto-Oncogene Proteins - metabolism</topic><topic>Proto-Oncogene Proteins c-akt</topic><topic>Receptors, Purinergic P1 - metabolism</topic><topic>Tritium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Akiba, Tetsuo</creatorcontrib><creatorcontrib>Yaguchi, Kuniko</creatorcontrib><creatorcontrib>Tsutsumi, Kikue</creatorcontrib><creatorcontrib>Nishioka, Tatsuo</creatorcontrib><creatorcontrib>Koyama, Ichiko</creatorcontrib><creatorcontrib>Nomura, Masaaki</creatorcontrib><creatorcontrib>Yokogawa, Koichi</creatorcontrib><creatorcontrib>Moritani, Shuzo</creatorcontrib><creatorcontrib>Miyamoto, Ken-ichi</creatorcontrib><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>Biochemical pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Akiba, Tetsuo</au><au>Yaguchi, Kuniko</au><au>Tsutsumi, Kikue</au><au>Nishioka, Tatsuo</au><au>Koyama, Ichiko</au><au>Nomura, Masaaki</au><au>Yokogawa, Koichi</au><au>Moritani, Shuzo</au><au>Miyamoto, Ken-ichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibitory mechanism of caffeine on insulin-stimulated glucose uptake in adipose cells</atitle><jtitle>Biochemical pharmacology</jtitle><addtitle>Biochem Pharmacol</addtitle><date>2004-11-15</date><risdate>2004</risdate><volume>68</volume><issue>10</issue><spage>1929</spage><epage>1937</epage><pages>1929-1937</pages><issn>0006-2952</issn><eissn>1873-2968</eissn><coden>BCPCA6</coden><abstract>Caffeine inhibits insulin-induced glucose uptake in rat adipocytes and also decreases insulin sensitivity, including whole-body glucose disposal and glucose uptake in skeletal muscle, during a euglycemic–hyperinsulinemic clamp in human. However, the mechanism by which caffeine decreases the insulin sensitivity is not still clear. We found that pre-treatment with caffeine inhibited the insulin-induced 2-deoxy-
d-[1-
3H]glucose uptake in a concentration-dependent manner in mouse preadipose MC-3T3-G2/PA6 cells differentiated into mature adipose cells. Caffeine also suppressed insulin-induced GLUT4 translocation in the differentiated cells. Although caffeine did not alter insulin-induced activation of PI3K and protein kinase C-zeta (PKCζ), an isoform of atypical PKC, which is reported to have an important role in insulin-induced GLUT4 translocation, we found that insulin-induced phosphorylation and activation of Akt were blocked by pre-treatment with caffeine. Inhibition of insulin-induced 2-deoxy-
d-[1-
3H]glucose uptake by caffeine was also observed in primary cultured brown adipocytes in a concentration-dependent manner. These results may, in part, explain the ability of caffeine to decrease insulin sensitivity.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>15476664</pmid><doi>10.1016/j.bcp.2004.07.036</doi><tpages>9</tpages></addata></record> |
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subjects | Adipocytes Adipocytes - drug effects Adipocytes - metabolism Akt Animals Biological and medical sciences Biological Transport Caffeine - pharmacology Cells, Cultured Cyclic AMP - metabolism Deoxyglucose - metabolism General and cellular metabolism. Vitamins Glucose - metabolism Glucose uptake GLUT4 Insulin Insulin - pharmacology Medical sciences Mice Mice, Inbred C57BL Pharmacology. Drug treatments Phosphatidylinositol 3-kinase Phosphatidylinositol 3-Kinases - metabolism Protein Kinase C - metabolism Protein-Serine-Threonine Kinases - metabolism Proto-Oncogene Proteins - metabolism Proto-Oncogene Proteins c-akt Receptors, Purinergic P1 - metabolism Tritium |
title | Inhibitory mechanism of caffeine on insulin-stimulated glucose uptake in adipose cells |
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