Modulating Effects of Chlorogenic Acid on Lipids and Glucose Metabolism and Expression of Hepatic Peroxisome Proliferator-activated Receptor-α in Golden Hamsters Fed on High Fat Diet
Objective To examine the effects of chlorogenic acid (CGA) on lipid and glucose metabolism under a high dietary fat burden and to explore the possible role of peroxisome proliferator-activated receptor-α (PPAR-α) in these effects. Methods Twenty male golden hamsters were randomly divided into CGA tr...
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description | Objective To examine the effects of chlorogenic acid (CGA) on lipid and glucose metabolism under a high dietary fat burden and to explore the possible role of peroxisome proliferator-activated receptor-α (PPAR-α) in these effects. Methods Twenty male golden hamsters were randomly divided into CGA treatment group (n=10, given peritoneal injection of CGA solution prepared with PBS, 80 mg CGA/kg body weight daily), and control group (n=10, given PBS i.p. at the average volume of the treatment group). Animals in both groups were given 15% high fat diet. Eight weeks after treatment with CGA, the level of biochemical parameters in fasting serum and tissues and the expression of hepatic mRNA and protein PPAR-α were determined. Results Eight weeks after treatment with CGA, the levels of fasting serum triglyceride (TG), free fatty acid (FFA), total cholesterol (TC), low density lipoprotein cholesterol (LDL-C), high density lipoprotein cholesterol (HDL-C), glucose (FSG), and insulin (FSI) were significantly lower in the GGA treatment group than in the control group. CGA also led to higher activity of hepatic lipase (HL) lower contents of TG and FFA in liver, and lower activity of lipoprotein lipase (LPL) in skeletal muscle. Furthermore, CGA significantly elevated significantly elevated the expression level of mRNA and protein expression in hepatic PPAR-α. Conclusion CGA can modify lipids and glucose metabolism, which may be attributed to PPAR-α facilitated lipid clearance in liver and improved insulin sensitivity. |
doi_str_mv | 10.1016/S0895-3988(09)60034-9 |
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Methods Twenty male golden hamsters were randomly divided into CGA treatment group (n=10, given peritoneal injection of CGA solution prepared with PBS, 80 mg CGA/kg body weight daily), and control group (n=10, given PBS i.p. at the average volume of the treatment group). Animals in both groups were given 15% high fat diet. Eight weeks after treatment with CGA, the level of biochemical parameters in fasting serum and tissues and the expression of hepatic mRNA and protein PPAR-α were determined. Results Eight weeks after treatment with CGA, the levels of fasting serum triglyceride (TG), free fatty acid (FFA), total cholesterol (TC), low density lipoprotein cholesterol (LDL-C), high density lipoprotein cholesterol (HDL-C), glucose (FSG), and insulin (FSI) were significantly lower in the GGA treatment group than in the control group. CGA also led to higher activity of hepatic lipase (HL) lower contents of TG and FFA in liver, and lower activity of lipoprotein lipase (LPL) in skeletal muscle. Furthermore, CGA significantly elevated significantly elevated the expression level of mRNA and protein expression in hepatic PPAR-α. Conclusion CGA can modify lipids and glucose metabolism, which may be attributed to PPAR-α facilitated lipid clearance in liver and improved insulin sensitivity.</description><identifier>ISSN: 0895-3988</identifier><identifier>EISSN: 2214-0190</identifier><identifier>DOI: 10.1016/S0895-3988(09)60034-9</identifier><identifier>PMID: 19618689</identifier><language>eng</language><publisher>China: Elsevier B.V</publisher><subject>Animals ; Blood Glucose - drug effects ; Chlorogenic acid ; Chlorogenic Acid - pharmacology ; Cricetinae ; Dietary Fats - pharmacology ; FFA drainage ; Gene Expression Regulation - drug effects ; Glucose - metabolism ; Golden hamster ; High fat diet ; Hypoglycemic effect ; Hypolipidemic Agents - pharmacology ; Hypolipidemic effect ; Insulin sensitivity ; Lipase - metabolism ; Lipid Metabolism - drug effects ; Lipids clearance ; Male ; Mesocricetus ; PPAR alpha - genetics ; PPAR alpha - metabolism ; PPAR-α ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Weight Gain ; 低密度脂蛋白胆固醇 ; 糖代谢 ; 绿原酸 ; 肝脏 ; 脂质 ; 过氧化物酶体增殖物激活受体 ; 金黄地鼠 ; 高脂饮食</subject><ispartof>Biomedical and environmental sciences, 2009-04, Vol.22 (2), p.122-129</ispartof><rights>2009 The Editorial Board of Biomedical and Environmental Sciences</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c437t-655651b70efbfddc281220e8407d27bd6bbd0db6455ddc5ff4a90472df08b72c3</citedby><cites>FETCH-LOGICAL-c437t-655651b70efbfddc281220e8407d27bd6bbd0db6455ddc5ff4a90472df08b72c3</cites></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/10.1016/S0895-3988(09)60034-9$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19618689$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LI, Shu-Yuan</creatorcontrib><creatorcontrib>CHANG, Cui-Qing</creatorcontrib><creatorcontrib>MA, Fu-Ying</creatorcontrib><creatorcontrib>YU, Chang-Long</creatorcontrib><title>Modulating Effects of Chlorogenic Acid on Lipids and Glucose Metabolism and Expression of Hepatic Peroxisome Proliferator-activated Receptor-α in Golden Hamsters Fed on High Fat Diet</title><title>Biomedical and environmental sciences</title><addtitle>Biomedical and Environmental Sciences</addtitle><description>Objective To examine the effects of chlorogenic acid (CGA) on lipid and glucose metabolism under a high dietary fat burden and to explore the possible role of peroxisome proliferator-activated receptor-α (PPAR-α) in these effects. Methods Twenty male golden hamsters were randomly divided into CGA treatment group (n=10, given peritoneal injection of CGA solution prepared with PBS, 80 mg CGA/kg body weight daily), and control group (n=10, given PBS i.p. at the average volume of the treatment group). Animals in both groups were given 15% high fat diet. Eight weeks after treatment with CGA, the level of biochemical parameters in fasting serum and tissues and the expression of hepatic mRNA and protein PPAR-α were determined. Results Eight weeks after treatment with CGA, the levels of fasting serum triglyceride (TG), free fatty acid (FFA), total cholesterol (TC), low density lipoprotein cholesterol (LDL-C), high density lipoprotein cholesterol (HDL-C), glucose (FSG), and insulin (FSI) were significantly lower in the GGA treatment group than in the control group. CGA also led to higher activity of hepatic lipase (HL) lower contents of TG and FFA in liver, and lower activity of lipoprotein lipase (LPL) in skeletal muscle. Furthermore, CGA significantly elevated significantly elevated the expression level of mRNA and protein expression in hepatic PPAR-α. Conclusion CGA can modify lipids and glucose metabolism, which may be attributed to PPAR-α facilitated lipid clearance in liver and improved insulin sensitivity.</description><subject>Animals</subject><subject>Blood Glucose - drug effects</subject><subject>Chlorogenic acid</subject><subject>Chlorogenic Acid - pharmacology</subject><subject>Cricetinae</subject><subject>Dietary Fats - pharmacology</subject><subject>FFA drainage</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Glucose - metabolism</subject><subject>Golden hamster</subject><subject>High fat diet</subject><subject>Hypoglycemic effect</subject><subject>Hypolipidemic Agents - pharmacology</subject><subject>Hypolipidemic effect</subject><subject>Insulin sensitivity</subject><subject>Lipase - metabolism</subject><subject>Lipid Metabolism - drug effects</subject><subject>Lipids clearance</subject><subject>Male</subject><subject>Mesocricetus</subject><subject>PPAR alpha - genetics</subject><subject>PPAR alpha - metabolism</subject><subject>PPAR-α</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Weight Gain</subject><subject>低密度脂蛋白胆固醇</subject><subject>糖代谢</subject><subject>绿原酸</subject><subject>肝脏</subject><subject>脂质</subject><subject>过氧化物酶体增殖物激活受体</subject><subject>金黄地鼠</subject><subject>高脂饮食</subject><issn>0895-3988</issn><issn>2214-0190</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkstu1DAUhiMEokPhEUAWCwSLgJ2LY6-qapgL0lRUXNaWYx_PGJI4tZ2qfayueAueCc9FsGRl6fg7_znW5yx7SfB7ggn98BUzXuclZ-wt5u8oxmWV80fZrChIlWPC8eNs9hc5y56F8APjivCKPc3OCKeEUcZn2a8rp6dORjts0cIYUDEgZ9B81znvtjBYhS6V1cgNaGNHqwOSg0arblIuALqCKFvX2dAfyou70UMINsEpYw1jylXoGry7s8H1gK59gg14GZ3PpYr2VkbQ6AsoGPel3w_IDmjlOg0DWss-RPABLeEwf223O7SUEX20EJ9nT4zsArw4nefZ9-Xi23ydbz6vPs0vN7mqyibmtK5pTdoGg2mN1qpgpCgwsAo3umhaTdtWY93Sqq7TbW1MJTmumkIbzNqmUOV59uaYO3p3M0GIordBQdfJAdwUBG1q3JQFTWB9BJV3IXgwYvS2l_5eECz2xsTBmNjrEJiLgzHBU9-r04Cp7UH_6zopSsDFEYD0zFsLXgRlYVCgrU-6hHb2vyNen1bbuWF7k1SLVqqfxnYgyvRVCKWs_AOvTbVX</recordid><startdate>20090401</startdate><enddate>20090401</enddate><creator>LI, Shu-Yuan</creator><creator>CHANG, Cui-Qing</creator><creator>MA, Fu-Ying</creator><creator>YU, Chang-Long</creator><general>Elsevier B.V</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>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20090401</creationdate><title>Modulating Effects of Chlorogenic Acid on Lipids and Glucose Metabolism and Expression of Hepatic Peroxisome Proliferator-activated Receptor-α in Golden Hamsters Fed on High Fat Diet</title><author>LI, Shu-Yuan ; CHANG, Cui-Qing ; MA, Fu-Ying ; YU, Chang-Long</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c437t-655651b70efbfddc281220e8407d27bd6bbd0db6455ddc5ff4a90472df08b72c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Blood Glucose - drug effects</topic><topic>Chlorogenic acid</topic><topic>Chlorogenic Acid - pharmacology</topic><topic>Cricetinae</topic><topic>Dietary Fats - pharmacology</topic><topic>FFA drainage</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Glucose - metabolism</topic><topic>Golden hamster</topic><topic>High fat diet</topic><topic>Hypoglycemic effect</topic><topic>Hypolipidemic Agents - pharmacology</topic><topic>Hypolipidemic effect</topic><topic>Insulin sensitivity</topic><topic>Lipase - metabolism</topic><topic>Lipid Metabolism - drug effects</topic><topic>Lipids clearance</topic><topic>Male</topic><topic>Mesocricetus</topic><topic>PPAR alpha - genetics</topic><topic>PPAR alpha - metabolism</topic><topic>PPAR-α</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Weight Gain</topic><topic>低密度脂蛋白胆固醇</topic><topic>糖代谢</topic><topic>绿原酸</topic><topic>肝脏</topic><topic>脂质</topic><topic>过氧化物酶体增殖物激活受体</topic><topic>金黄地鼠</topic><topic>高脂饮食</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LI, Shu-Yuan</creatorcontrib><creatorcontrib>CHANG, Cui-Qing</creatorcontrib><creatorcontrib>MA, Fu-Ying</creatorcontrib><creatorcontrib>YU, Chang-Long</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>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biomedical and environmental sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LI, Shu-Yuan</au><au>CHANG, Cui-Qing</au><au>MA, Fu-Ying</au><au>YU, Chang-Long</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modulating Effects of Chlorogenic Acid on Lipids and Glucose Metabolism and Expression of Hepatic Peroxisome Proliferator-activated Receptor-α in Golden Hamsters Fed on High Fat Diet</atitle><jtitle>Biomedical and environmental sciences</jtitle><addtitle>Biomedical and Environmental Sciences</addtitle><date>2009-04-01</date><risdate>2009</risdate><volume>22</volume><issue>2</issue><spage>122</spage><epage>129</epage><pages>122-129</pages><issn>0895-3988</issn><eissn>2214-0190</eissn><abstract>Objective To examine the effects of chlorogenic acid (CGA) on lipid and glucose metabolism under a high dietary fat burden and to explore the possible role of peroxisome proliferator-activated receptor-α (PPAR-α) in these effects. Methods Twenty male golden hamsters were randomly divided into CGA treatment group (n=10, given peritoneal injection of CGA solution prepared with PBS, 80 mg CGA/kg body weight daily), and control group (n=10, given PBS i.p. at the average volume of the treatment group). Animals in both groups were given 15% high fat diet. Eight weeks after treatment with CGA, the level of biochemical parameters in fasting serum and tissues and the expression of hepatic mRNA and protein PPAR-α were determined. Results Eight weeks after treatment with CGA, the levels of fasting serum triglyceride (TG), free fatty acid (FFA), total cholesterol (TC), low density lipoprotein cholesterol (LDL-C), high density lipoprotein cholesterol (HDL-C), glucose (FSG), and insulin (FSI) were significantly lower in the GGA treatment group than in the control group. CGA also led to higher activity of hepatic lipase (HL) lower contents of TG and FFA in liver, and lower activity of lipoprotein lipase (LPL) in skeletal muscle. Furthermore, CGA significantly elevated significantly elevated the expression level of mRNA and protein expression in hepatic PPAR-α. Conclusion CGA can modify lipids and glucose metabolism, which may be attributed to PPAR-α facilitated lipid clearance in liver and improved insulin sensitivity.</abstract><cop>China</cop><pub>Elsevier B.V</pub><pmid>19618689</pmid><doi>10.1016/S0895-3988(09)60034-9</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Blood Glucose - drug effects Chlorogenic acid Chlorogenic Acid - pharmacology Cricetinae Dietary Fats - pharmacology FFA drainage Gene Expression Regulation - drug effects Glucose - metabolism Golden hamster High fat diet Hypoglycemic effect Hypolipidemic Agents - pharmacology Hypolipidemic effect Insulin sensitivity Lipase - metabolism Lipid Metabolism - drug effects Lipids clearance Male Mesocricetus PPAR alpha - genetics PPAR alpha - metabolism PPAR-α RNA, Messenger - genetics RNA, Messenger - metabolism Weight Gain 低密度脂蛋白胆固醇 糖代谢 绿原酸 肝脏 脂质 过氧化物酶体增殖物激活受体 金黄地鼠 高脂饮食 |
title | Modulating Effects of Chlorogenic Acid on Lipids and Glucose Metabolism and Expression of Hepatic Peroxisome Proliferator-activated Receptor-α in Golden Hamsters Fed on High Fat Diet |
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