Chlorogenic Acid Maintains Glucose Homeostasis through Modulating the Expression of SGLT-1,GLUT-2,and PLG in Different Intestinal Segments of Sprague-Dawley Rats Fed a High-Fat Diet
Objective To reveal the effects and related mechanisms of chlorogenic acid(CGA)on intestinal glucose homeostasis.Methods Forty male Sprague-Dawley rats were randomly and equally divided into four groups:normal chow(NC),high-fat diet(HFD),HFD with low-dose CGA(20 mg/kg,HFD-LC),and HFD with high-dose...
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description | Objective To reveal the effects and related mechanisms of chlorogenic acid(CGA)on intestinal glucose homeostasis.Methods Forty male Sprague-Dawley rats were randomly and equally divided into four groups:normal chow(NC),high-fat diet(HFD),HFD with low-dose CGA(20 mg/kg,HFD-LC),and HFD with high-dose CGA(90 mg/kg,HFD-HC).The oral glucose tolerance test was performed,and fast serum insulin(FSI)was detected using an enzyme-linked immunosorbent assay.The m RNA expression levels of glucose transporters(Sglt-1 and Glut-2)and proglucagon(Plg)in different intestinal segments(the duodenum,jejunum,ileum,and colon)were analyzed using quantitative real-time polymerase chain reaction.SGLT-1 protein and the morphology of epithelial cells in the duodenum and jejunum was localized by using immunofluorescence.Results At both doses,CGA ameliorated the HFD-induced body weight gain,maintained FSI,and increased postprandial 30-min glucagon-like peptide 1 secretion.High-dose CGA inhibited the HFD-induced elevation in Sglt-1 expression.Both CGA doses normalized the HFD-induced downregulation of Glut-2 and elevated the expression of Plg in all four intestinal segments.Conclusion An HFD can cause a glucose metabolism disorder in the rat intestine and affect body glucose homeostasis.CGA can modify intestinal glucose metabolism by regulating the expression of intestinal glucose transporters and Plg,thereby controlling the levels of blood glucose and insulin to maintain glucose homeostasis. |
doi_str_mv | 10.3967/bes2015.123 |
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fullrecord | <record><control><sourceid>wanfang_jour_proqu</sourceid><recordid>TN_cdi_wanfang_journals_bes201512005</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cqvip_id>667748294</cqvip_id><wanfj_id>bes201512005</wanfj_id><els_id>S0895398816300058</els_id><sourcerecordid>bes201512005</sourcerecordid><originalsourceid>FETCH-LOGICAL-c355t-4810ba8a8c2ab144b308a90238ddea8568fc04f3f83862824aa07ca5f6608c2c3</originalsourceid><addsrcrecordid>eNo9kU9v1DAQxSMEokvhxB1ZqAcOTbGdf86x2nazlVKB6PZsTZxJ4iqxt3ZC6Qfj-2HYLQfL0tPvPc3Mi6KPjF4kZV58bdBzyrILxpNX0YpzlsaUlfR1tKKizOKkFOIkeuf9A6UpK1PxNjrheVEUJS1X0e_1MFpnezRakUulW3IL2szheVKNi7IeydZOaP0MXnsyD84u_UBubbuMMGvTBwnJ9a-9Q--1NcR25K6qdzE7r-r7XczPwbTke10RbciV7jp0aGZyY2b0wQ4jucN-CpL_59w76BeMr-BpxGfyA4K8wZYA2ep-iDcwhwyc30dvOhg9fjj-p9H95nq33sb1t-pmfVnHKsmyOU4Fow0IEIpDw9K0SaiAkvJEtC2CyHLRKZp2SScSkXPBUwBaKMi6PKfBo5LT6OyQ-wSmA9PLB7u4MLOXx6MzTmkWsC8HbO_s4xL2kpP2CscRDNrFS1aEvHDvggb00xFdmglbuXd6AvcsXxoJQHYAMOz1U6OTXmk0ClvtUM2ytVoyKv82_zKEDM0H3-eDTw3W9I-hmP_ZechOBS_T5A9z5Kns</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1760879070</pqid></control><display><type>article</type><title>Chlorogenic Acid Maintains Glucose Homeostasis through Modulating the Expression of SGLT-1,GLUT-2,and PLG in Different Intestinal Segments of Sprague-Dawley Rats Fed a High-Fat Diet</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>PENG, Bing Jie ; ZHU, Qi ; ZHONG, Ying Li ; XU, Shi Hao ; WANG, Zheng</creator><creatorcontrib>PENG, Bing Jie ; ZHU, Qi ; ZHONG, Ying Li ; XU, Shi Hao ; WANG, Zheng</creatorcontrib><description>Objective To reveal the effects and related mechanisms of chlorogenic acid(CGA)on intestinal glucose homeostasis.Methods Forty male Sprague-Dawley rats were randomly and equally divided into four groups:normal chow(NC),high-fat diet(HFD),HFD with low-dose CGA(20 mg/kg,HFD-LC),and HFD with high-dose CGA(90 mg/kg,HFD-HC).The oral glucose tolerance test was performed,and fast serum insulin(FSI)was detected using an enzyme-linked immunosorbent assay.The m RNA expression levels of glucose transporters(Sglt-1 and Glut-2)and proglucagon(Plg)in different intestinal segments(the duodenum,jejunum,ileum,and colon)were analyzed using quantitative real-time polymerase chain reaction.SGLT-1 protein and the morphology of epithelial cells in the duodenum and jejunum was localized by using immunofluorescence.Results At both doses,CGA ameliorated the HFD-induced body weight gain,maintained FSI,and increased postprandial 30-min glucagon-like peptide 1 secretion.High-dose CGA inhibited the HFD-induced elevation in Sglt-1 expression.Both CGA doses normalized the HFD-induced downregulation of Glut-2 and elevated the expression of Plg in all four intestinal segments.Conclusion An HFD can cause a glucose metabolism disorder in the rat intestine and affect body glucose homeostasis.CGA can modify intestinal glucose metabolism by regulating the expression of intestinal glucose transporters and Plg,thereby controlling the levels of blood glucose and insulin to maintain glucose homeostasis.</description><identifier>ISSN: 0895-3988</identifier><identifier>EISSN: 2214-0190</identifier><identifier>DOI: 10.3967/bes2015.123</identifier><identifier>PMID: 26777909</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Chlorogenic acid ; Chlorogenic Acid - pharmacology ; Diet, High-Fat - adverse effects ; duodenum ; GLP-1 ; glucagon ; Glucagon-Like Peptide 1 - metabolism ; Glucose ; Glucose - metabolism ; Glucose homeostasis ; Glucose Tolerance Test ; Glucose Transporter Type 2 - metabolism ; GLUT-2 ; High-fat diet ; Homeostasis ; immunosorbent ; Insulin - blood ; Intestine ; Intestines - drug effects ; Intestines - metabolism ; maintain ; Male ; metabolism ; PLG ; Proglucagon - metabolism ; Random Allocation ; Rats, Sprague-Dawley ; secretion ; SGLT-1 ; Sodium-Glucose Transporter 1 - metabolism ; transporters ; Weight Gain - drug effects</subject><ispartof>Biomedical and environmental sciences, 2015-12, Vol.28 (12), p.894-903</ispartof><rights>2015 The Editorial Board of Biomedical and Environmental Sciences</rights><rights>Copyright © 2015 The Editorial Board of Biomedical and Environmental Sciences. Published by China CDC. All rights reserved.</rights><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c355t-4810ba8a8c2ab144b308a90238ddea8568fc04f3f83862824aa07ca5f6608c2c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/84046X/84046X.jpg</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.3967/bes2015.123$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26777909$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>PENG, Bing Jie</creatorcontrib><creatorcontrib>ZHU, Qi</creatorcontrib><creatorcontrib>ZHONG, Ying Li</creatorcontrib><creatorcontrib>XU, Shi Hao</creatorcontrib><creatorcontrib>WANG, Zheng</creatorcontrib><title>Chlorogenic Acid Maintains Glucose Homeostasis through Modulating the Expression of SGLT-1,GLUT-2,and PLG in Different Intestinal Segments of Sprague-Dawley Rats Fed a High-Fat Diet</title><title>Biomedical and environmental sciences</title><addtitle>Biomedical and Environmental Sciences</addtitle><description>Objective To reveal the effects and related mechanisms of chlorogenic acid(CGA)on intestinal glucose homeostasis.Methods Forty male Sprague-Dawley rats were randomly and equally divided into four groups:normal chow(NC),high-fat diet(HFD),HFD with low-dose CGA(20 mg/kg,HFD-LC),and HFD with high-dose CGA(90 mg/kg,HFD-HC).The oral glucose tolerance test was performed,and fast serum insulin(FSI)was detected using an enzyme-linked immunosorbent assay.The m RNA expression levels of glucose transporters(Sglt-1 and Glut-2)and proglucagon(Plg)in different intestinal segments(the duodenum,jejunum,ileum,and colon)were analyzed using quantitative real-time polymerase chain reaction.SGLT-1 protein and the morphology of epithelial cells in the duodenum and jejunum was localized by using immunofluorescence.Results At both doses,CGA ameliorated the HFD-induced body weight gain,maintained FSI,and increased postprandial 30-min glucagon-like peptide 1 secretion.High-dose CGA inhibited the HFD-induced elevation in Sglt-1 expression.Both CGA doses normalized the HFD-induced downregulation of Glut-2 and elevated the expression of Plg in all four intestinal segments.Conclusion An HFD can cause a glucose metabolism disorder in the rat intestine and affect body glucose homeostasis.CGA can modify intestinal glucose metabolism by regulating the expression of intestinal glucose transporters and Plg,thereby controlling the levels of blood glucose and insulin to maintain glucose homeostasis.</description><subject>Animals</subject><subject>Chlorogenic acid</subject><subject>Chlorogenic Acid - pharmacology</subject><subject>Diet, High-Fat - adverse effects</subject><subject>duodenum</subject><subject>GLP-1</subject><subject>glucagon</subject><subject>Glucagon-Like Peptide 1 - metabolism</subject><subject>Glucose</subject><subject>Glucose - metabolism</subject><subject>Glucose homeostasis</subject><subject>Glucose Tolerance Test</subject><subject>Glucose Transporter Type 2 - metabolism</subject><subject>GLUT-2</subject><subject>High-fat diet</subject><subject>Homeostasis</subject><subject>immunosorbent</subject><subject>Insulin - blood</subject><subject>Intestine</subject><subject>Intestines - drug effects</subject><subject>Intestines - metabolism</subject><subject>maintain</subject><subject>Male</subject><subject>metabolism</subject><subject>PLG</subject><subject>Proglucagon - metabolism</subject><subject>Random Allocation</subject><subject>Rats, Sprague-Dawley</subject><subject>secretion</subject><subject>SGLT-1</subject><subject>Sodium-Glucose Transporter 1 - metabolism</subject><subject>transporters</subject><subject>Weight Gain - drug effects</subject><issn>0895-3988</issn><issn>2214-0190</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kU9v1DAQxSMEokvhxB1ZqAcOTbGdf86x2nazlVKB6PZsTZxJ4iqxt3ZC6Qfj-2HYLQfL0tPvPc3Mi6KPjF4kZV58bdBzyrILxpNX0YpzlsaUlfR1tKKizOKkFOIkeuf9A6UpK1PxNjrheVEUJS1X0e_1MFpnezRakUulW3IL2szheVKNi7IeydZOaP0MXnsyD84u_UBubbuMMGvTBwnJ9a-9Q--1NcR25K6qdzE7r-r7XczPwbTke10RbciV7jp0aGZyY2b0wQ4jucN-CpL_59w76BeMr-BpxGfyA4K8wZYA2ep-iDcwhwyc30dvOhg9fjj-p9H95nq33sb1t-pmfVnHKsmyOU4Fow0IEIpDw9K0SaiAkvJEtC2CyHLRKZp2SScSkXPBUwBaKMi6PKfBo5LT6OyQ-wSmA9PLB7u4MLOXx6MzTmkWsC8HbO_s4xL2kpP2CscRDNrFS1aEvHDvggb00xFdmglbuXd6AvcsXxoJQHYAMOz1U6OTXmk0ClvtUM2ytVoyKv82_zKEDM0H3-eDTw3W9I-hmP_ZechOBS_T5A9z5Kns</recordid><startdate>20151201</startdate><enddate>20151201</enddate><creator>PENG, Bing Jie</creator><creator>ZHU, Qi</creator><creator>ZHONG, Ying Li</creator><creator>XU, Shi Hao</creator><creator>WANG, Zheng</creator><general>Elsevier B.V</general><general>College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha 410128, Hunan, China</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20151201</creationdate><title>Chlorogenic Acid Maintains Glucose Homeostasis through Modulating the Expression of SGLT-1,GLUT-2,and PLG in Different Intestinal Segments of Sprague-Dawley Rats Fed a High-Fat Diet</title><author>PENG, Bing Jie ; ZHU, Qi ; ZHONG, Ying Li ; XU, Shi Hao ; WANG, Zheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c355t-4810ba8a8c2ab144b308a90238ddea8568fc04f3f83862824aa07ca5f6608c2c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Chlorogenic acid</topic><topic>Chlorogenic Acid - pharmacology</topic><topic>Diet, High-Fat - adverse effects</topic><topic>duodenum</topic><topic>GLP-1</topic><topic>glucagon</topic><topic>Glucagon-Like Peptide 1 - metabolism</topic><topic>Glucose</topic><topic>Glucose - metabolism</topic><topic>Glucose homeostasis</topic><topic>Glucose Tolerance Test</topic><topic>Glucose Transporter Type 2 - metabolism</topic><topic>GLUT-2</topic><topic>High-fat diet</topic><topic>Homeostasis</topic><topic>immunosorbent</topic><topic>Insulin - blood</topic><topic>Intestine</topic><topic>Intestines - drug effects</topic><topic>Intestines - metabolism</topic><topic>maintain</topic><topic>Male</topic><topic>metabolism</topic><topic>PLG</topic><topic>Proglucagon - metabolism</topic><topic>Random Allocation</topic><topic>Rats, Sprague-Dawley</topic><topic>secretion</topic><topic>SGLT-1</topic><topic>Sodium-Glucose Transporter 1 - metabolism</topic><topic>transporters</topic><topic>Weight Gain - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>PENG, Bing Jie</creatorcontrib><creatorcontrib>ZHU, Qi</creatorcontrib><creatorcontrib>ZHONG, Ying Li</creatorcontrib><creatorcontrib>XU, Shi Hao</creatorcontrib><creatorcontrib>WANG, Zheng</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Biomedical and environmental sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>PENG, Bing Jie</au><au>ZHU, Qi</au><au>ZHONG, Ying Li</au><au>XU, Shi Hao</au><au>WANG, Zheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chlorogenic Acid Maintains Glucose Homeostasis through Modulating the Expression of SGLT-1,GLUT-2,and PLG in Different Intestinal Segments of Sprague-Dawley Rats Fed a High-Fat Diet</atitle><jtitle>Biomedical and environmental sciences</jtitle><addtitle>Biomedical and Environmental Sciences</addtitle><date>2015-12-01</date><risdate>2015</risdate><volume>28</volume><issue>12</issue><spage>894</spage><epage>903</epage><pages>894-903</pages><issn>0895-3988</issn><eissn>2214-0190</eissn><abstract>Objective To reveal the effects and related mechanisms of chlorogenic acid(CGA)on intestinal glucose homeostasis.Methods Forty male Sprague-Dawley rats were randomly and equally divided into four groups:normal chow(NC),high-fat diet(HFD),HFD with low-dose CGA(20 mg/kg,HFD-LC),and HFD with high-dose CGA(90 mg/kg,HFD-HC).The oral glucose tolerance test was performed,and fast serum insulin(FSI)was detected using an enzyme-linked immunosorbent assay.The m RNA expression levels of glucose transporters(Sglt-1 and Glut-2)and proglucagon(Plg)in different intestinal segments(the duodenum,jejunum,ileum,and colon)were analyzed using quantitative real-time polymerase chain reaction.SGLT-1 protein and the morphology of epithelial cells in the duodenum and jejunum was localized by using immunofluorescence.Results At both doses,CGA ameliorated the HFD-induced body weight gain,maintained FSI,and increased postprandial 30-min glucagon-like peptide 1 secretion.High-dose CGA inhibited the HFD-induced elevation in Sglt-1 expression.Both CGA doses normalized the HFD-induced downregulation of Glut-2 and elevated the expression of Plg in all four intestinal segments.Conclusion An HFD can cause a glucose metabolism disorder in the rat intestine and affect body glucose homeostasis.CGA can modify intestinal glucose metabolism by regulating the expression of intestinal glucose transporters and Plg,thereby controlling the levels of blood glucose and insulin to maintain glucose homeostasis.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>26777909</pmid><doi>10.3967/bes2015.123</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Chlorogenic acid Chlorogenic Acid - pharmacology Diet, High-Fat - adverse effects duodenum GLP-1 glucagon Glucagon-Like Peptide 1 - metabolism Glucose Glucose - metabolism Glucose homeostasis Glucose Tolerance Test Glucose Transporter Type 2 - metabolism GLUT-2 High-fat diet Homeostasis immunosorbent Insulin - blood Intestine Intestines - drug effects Intestines - metabolism maintain Male metabolism PLG Proglucagon - metabolism Random Allocation Rats, Sprague-Dawley secretion SGLT-1 Sodium-Glucose Transporter 1 - metabolism transporters Weight Gain - drug effects |
title | Chlorogenic Acid Maintains Glucose Homeostasis through Modulating the Expression of SGLT-1,GLUT-2,and PLG in Different Intestinal Segments of Sprague-Dawley Rats Fed a High-Fat Diet |
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