Effects of quercetin on hepatic fibroblast growth factor-21 (FGF-21) and peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) levels in rats fed with high fructose
Background Available studies show that quercetin reduces Metabolic Syndrome (MetS) and its complications, increases insulin sensitivity and improves glucose levels. It has been reported that the increase in hepatic gene expressions of fibroblast growth factor-21 (FGF-21), an important metabolic regu...
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description | Background
Available studies show that quercetin reduces Metabolic Syndrome (MetS) and its complications, increases insulin sensitivity and improves glucose levels. It has been reported that the increase in hepatic gene expressions of fibroblast growth factor-21 (FGF-21), an important metabolic regulator of insulin sensitivity, glucose and energy homeostasis, and peroxisome proliferator-activated receptor gamma coactivator-1α (PGC-1α), which plays a central role in the regulation of cellular energy metabolism, eliminate the negative effects of fructose in fructose-fed rats. The main purpose of our study is to examine the effects of quercetin on hepatic FGF-21 and PGC-1α expressions and levels, as well as its protective and therapeutic role on MetS components in rats fed with fructose.
Methods and results
In our study, 24 Sprague Dawley male rats were divided into 4 groups: control, fructose, quercetin, fructose+quercetin (
n
= 6). During the 10-week experiment, quercetin was administered at a daily dose of 15 mg/kg body weight and fructose at a rate of 20%. Blood pressure and weights of all groups were measured and recorded. At the end of week 10, blood and liver tissue samples were taken. Serum insulin, glucose and triglyceride, total, HDL and VLDL cholesterol levels were determined from the samples. Insulin resistance was calculated using the HOMA-IR formula. Hepatic PGC-1α and FGF-21 protein levels and their mRNA expressions were determined. Criteria for metabolic syndrome were successfully established with fructose. It was observed that the administration of quercetin alone and in combination with fructose exerted positive effects and improved MetS criteria. It was determined that the administration of quercetin increased hepatic FGF-21 and PGC-1α protein levels and Messenger RNA (mRNA) expressions of them, which were decreased by fructose application.
Conclusions
The results of our study showed that 10-week administration of quercetin at 15 mg/kg exerted beneficial effects on lipid and carbohydrate metabolism in the fructose-mediated MetS model; therefore, quercetin may have great potential in the prevention and treatment of metabolic disorders. |
doi_str_mv | 10.1007/s11033-023-08444-y |
format | Article |
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Available studies show that quercetin reduces Metabolic Syndrome (MetS) and its complications, increases insulin sensitivity and improves glucose levels. It has been reported that the increase in hepatic gene expressions of fibroblast growth factor-21 (FGF-21), an important metabolic regulator of insulin sensitivity, glucose and energy homeostasis, and peroxisome proliferator-activated receptor gamma coactivator-1α (PGC-1α), which plays a central role in the regulation of cellular energy metabolism, eliminate the negative effects of fructose in fructose-fed rats. The main purpose of our study is to examine the effects of quercetin on hepatic FGF-21 and PGC-1α expressions and levels, as well as its protective and therapeutic role on MetS components in rats fed with fructose.
Methods and results
In our study, 24 Sprague Dawley male rats were divided into 4 groups: control, fructose, quercetin, fructose+quercetin (
n
= 6). During the 10-week experiment, quercetin was administered at a daily dose of 15 mg/kg body weight and fructose at a rate of 20%. Blood pressure and weights of all groups were measured and recorded. At the end of week 10, blood and liver tissue samples were taken. Serum insulin, glucose and triglyceride, total, HDL and VLDL cholesterol levels were determined from the samples. Insulin resistance was calculated using the HOMA-IR formula. Hepatic PGC-1α and FGF-21 protein levels and their mRNA expressions were determined. Criteria for metabolic syndrome were successfully established with fructose. It was observed that the administration of quercetin alone and in combination with fructose exerted positive effects and improved MetS criteria. It was determined that the administration of quercetin increased hepatic FGF-21 and PGC-1α protein levels and Messenger RNA (mRNA) expressions of them, which were decreased by fructose application.
Conclusions
The results of our study showed that 10-week administration of quercetin at 15 mg/kg exerted beneficial effects on lipid and carbohydrate metabolism in the fructose-mediated MetS model; therefore, quercetin may have great potential in the prevention and treatment of metabolic disorders.</description><identifier>ISSN: 0301-4851</identifier><identifier>EISSN: 1573-4978</identifier><identifier>DOI: 10.1007/s11033-023-08444-y</identifier><identifier>PMID: 37086297</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Animal Anatomy ; Animal Biochemistry ; Animals ; Biomedical and Life Sciences ; Blood pressure ; blood serum ; Body weight ; Carbohydrate metabolism ; Cholesterol ; energy ; Energy balance ; Energy metabolism ; Fibroblast growth factors ; Fibroblast Growth Factors - metabolism ; Fibroblasts ; Fructose ; Fructose - metabolism ; Fructose - pharmacology ; genes ; Glucose ; Glucose - metabolism ; Growth factors ; High density lipoprotein ; Histology ; Homeostasis ; insulin ; Insulin Resistance ; Life Sciences ; Lipid metabolism ; Lipoproteins (very low density) ; Liver ; Liver - metabolism ; Male ; males ; messenger RNA ; Metabolic disorders ; Metabolic syndrome ; Metabolic Syndrome - metabolism ; Morphology ; mRNA ; Original Article ; peroxisome proliferator-activated receptor gamma ; Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - genetics ; Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - metabolism ; Peroxisome proliferator-activated receptors ; Quercetin ; Quercetin - metabolism ; Quercetin - pharmacology ; Rats ; Rats, Sprague-Dawley ; RNA, Messenger - metabolism ; therapeutics ; triacylglycerols ; very low density lipoprotein</subject><ispartof>Molecular biology reports, 2023-06, Vol.50 (6), p.4983-4997</ispartof><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2023. The Author(s), under exclusive licence to Springer Nature B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c359t-61e9b3125214cad2c46c87d512bae95e4cebfdb00b2f162ec6baac2b97c587003</cites><orcidid>0000-0002-2884-4753 ; 0000-0002-5749-5687 ; 0000-0002-0629-034X ; 0000-0002-8945-3801 ; 0000-0002-6799-6522</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11033-023-08444-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11033-023-08444-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37086297$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kocaman Kalkan, Kardelen</creatorcontrib><creatorcontrib>Şen, Serkan</creatorcontrib><creatorcontrib>Narlı, Belkıs</creatorcontrib><creatorcontrib>Seymen, Cemile Merve</creatorcontrib><creatorcontrib>Yılmaz, Canan</creatorcontrib><title>Effects of quercetin on hepatic fibroblast growth factor-21 (FGF-21) and peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) levels in rats fed with high fructose</title><title>Molecular biology reports</title><addtitle>Mol Biol Rep</addtitle><addtitle>Mol Biol Rep</addtitle><description>Background
Available studies show that quercetin reduces Metabolic Syndrome (MetS) and its complications, increases insulin sensitivity and improves glucose levels. It has been reported that the increase in hepatic gene expressions of fibroblast growth factor-21 (FGF-21), an important metabolic regulator of insulin sensitivity, glucose and energy homeostasis, and peroxisome proliferator-activated receptor gamma coactivator-1α (PGC-1α), which plays a central role in the regulation of cellular energy metabolism, eliminate the negative effects of fructose in fructose-fed rats. The main purpose of our study is to examine the effects of quercetin on hepatic FGF-21 and PGC-1α expressions and levels, as well as its protective and therapeutic role on MetS components in rats fed with fructose.
Methods and results
In our study, 24 Sprague Dawley male rats were divided into 4 groups: control, fructose, quercetin, fructose+quercetin (
n
= 6). During the 10-week experiment, quercetin was administered at a daily dose of 15 mg/kg body weight and fructose at a rate of 20%. Blood pressure and weights of all groups were measured and recorded. At the end of week 10, blood and liver tissue samples were taken. Serum insulin, glucose and triglyceride, total, HDL and VLDL cholesterol levels were determined from the samples. Insulin resistance was calculated using the HOMA-IR formula. Hepatic PGC-1α and FGF-21 protein levels and their mRNA expressions were determined. Criteria for metabolic syndrome were successfully established with fructose. It was observed that the administration of quercetin alone and in combination with fructose exerted positive effects and improved MetS criteria. It was determined that the administration of quercetin increased hepatic FGF-21 and PGC-1α protein levels and Messenger RNA (mRNA) expressions of them, which were decreased by fructose application.
Conclusions
The results of our study showed that 10-week administration of quercetin at 15 mg/kg exerted beneficial effects on lipid and carbohydrate metabolism in the fructose-mediated MetS model; therefore, quercetin may have great potential in the prevention and treatment of metabolic disorders.</description><subject>Animal Anatomy</subject><subject>Animal Biochemistry</subject><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Blood pressure</subject><subject>blood serum</subject><subject>Body weight</subject><subject>Carbohydrate metabolism</subject><subject>Cholesterol</subject><subject>energy</subject><subject>Energy balance</subject><subject>Energy metabolism</subject><subject>Fibroblast growth factors</subject><subject>Fibroblast Growth Factors - metabolism</subject><subject>Fibroblasts</subject><subject>Fructose</subject><subject>Fructose - metabolism</subject><subject>Fructose - pharmacology</subject><subject>genes</subject><subject>Glucose</subject><subject>Glucose - metabolism</subject><subject>Growth factors</subject><subject>High density lipoprotein</subject><subject>Histology</subject><subject>Homeostasis</subject><subject>insulin</subject><subject>Insulin Resistance</subject><subject>Life Sciences</subject><subject>Lipid metabolism</subject><subject>Lipoproteins (very low density)</subject><subject>Liver</subject><subject>Liver - metabolism</subject><subject>Male</subject><subject>males</subject><subject>messenger RNA</subject><subject>Metabolic disorders</subject><subject>Metabolic syndrome</subject><subject>Metabolic Syndrome - metabolism</subject><subject>Morphology</subject><subject>mRNA</subject><subject>Original Article</subject><subject>peroxisome proliferator-activated receptor gamma</subject><subject>Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - genetics</subject><subject>Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - metabolism</subject><subject>Peroxisome proliferator-activated receptors</subject><subject>Quercetin</subject><subject>Quercetin - metabolism</subject><subject>Quercetin - pharmacology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>RNA, Messenger - metabolism</subject><subject>therapeutics</subject><subject>triacylglycerols</subject><subject>very low density lipoprotein</subject><issn>0301-4851</issn><issn>1573-4978</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFksFu1DAQhiMEotvCC3BAlrhsDwGPHcfJEa26C1IlOMA5cpzxrqskDna2ZR-LB-AVeKZO2QUkDnCwRvJ888-M_WfZC-CvgXP9JgFwKXMu6FRFUeSHR9kClJZ5UevqcbbgkkNeVArOsvOUbjjnBWj1NDuTmlelqPUi-37lHNo5seDYlz1Gi7MfWRjZDicze8ucb2Noe5Nmto3hbt4xZ-wcYi6ALdebNcVLZsaOTRjDV5_CgGyKofcOo3ngiPa3ZsaORbQ40RXbmmEwzIZTim4gN_20M2z5cbPK4ce3S9bjLfaJ0TAkk5ij-jtP3Xd-SyPEPc2Q8Fn2xJk-4fNTvMg-r68-rd7l1x8271dvr3MrVT3nJWDdShBKQGFNJ2xR2kp3CkRrsFZYWGxd13LeCgelQFu2xljR1tqqSnMuL7LlUZc2o1dKczP4ZLHvzYhhnxoJSkKtRV39FxUVV1xUGkpCX_2F3oR9HGkRoqBSihcSiBJHysaQUkTXTNEPJh4a4M2DD5qjDxryQfPTB82Bil6epPftgN3vkl8fT4A8AolS4xbjn97_kL0HbnfARw</recordid><startdate>20230601</startdate><enddate>20230601</enddate><creator>Kocaman Kalkan, Kardelen</creator><creator>Şen, Serkan</creator><creator>Narlı, Belkıs</creator><creator>Seymen, Cemile Merve</creator><creator>Yılmaz, Canan</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><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>3V.</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0002-2884-4753</orcidid><orcidid>https://orcid.org/0000-0002-5749-5687</orcidid><orcidid>https://orcid.org/0000-0002-0629-034X</orcidid><orcidid>https://orcid.org/0000-0002-8945-3801</orcidid><orcidid>https://orcid.org/0000-0002-6799-6522</orcidid></search><sort><creationdate>20230601</creationdate><title>Effects of quercetin on hepatic fibroblast growth factor-21 (FGF-21) and peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) levels in rats fed with high fructose</title><author>Kocaman Kalkan, Kardelen ; Şen, Serkan ; Narlı, Belkıs ; Seymen, Cemile Merve ; Yılmaz, Canan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-61e9b3125214cad2c46c87d512bae95e4cebfdb00b2f162ec6baac2b97c587003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animal Anatomy</topic><topic>Animal Biochemistry</topic><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Blood pressure</topic><topic>blood serum</topic><topic>Body weight</topic><topic>Carbohydrate metabolism</topic><topic>Cholesterol</topic><topic>energy</topic><topic>Energy balance</topic><topic>Energy metabolism</topic><topic>Fibroblast growth factors</topic><topic>Fibroblast Growth Factors - metabolism</topic><topic>Fibroblasts</topic><topic>Fructose</topic><topic>Fructose - metabolism</topic><topic>Fructose - pharmacology</topic><topic>genes</topic><topic>Glucose</topic><topic>Glucose - metabolism</topic><topic>Growth factors</topic><topic>High density lipoprotein</topic><topic>Histology</topic><topic>Homeostasis</topic><topic>insulin</topic><topic>Insulin Resistance</topic><topic>Life Sciences</topic><topic>Lipid metabolism</topic><topic>Lipoproteins (very low density)</topic><topic>Liver</topic><topic>Liver - metabolism</topic><topic>Male</topic><topic>males</topic><topic>messenger RNA</topic><topic>Metabolic disorders</topic><topic>Metabolic syndrome</topic><topic>Metabolic Syndrome - metabolism</topic><topic>Morphology</topic><topic>mRNA</topic><topic>Original Article</topic><topic>peroxisome proliferator-activated receptor gamma</topic><topic>Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - genetics</topic><topic>Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - metabolism</topic><topic>Peroxisome proliferator-activated receptors</topic><topic>Quercetin</topic><topic>Quercetin - metabolism</topic><topic>Quercetin - pharmacology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>RNA, Messenger - metabolism</topic><topic>therapeutics</topic><topic>triacylglycerols</topic><topic>very low density lipoprotein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kocaman Kalkan, Kardelen</creatorcontrib><creatorcontrib>Şen, Serkan</creatorcontrib><creatorcontrib>Narlı, Belkıs</creatorcontrib><creatorcontrib>Seymen, Cemile Merve</creatorcontrib><creatorcontrib>Yılmaz, Canan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</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>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Molecular biology reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kocaman Kalkan, Kardelen</au><au>Şen, Serkan</au><au>Narlı, Belkıs</au><au>Seymen, Cemile Merve</au><au>Yılmaz, Canan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of quercetin on hepatic fibroblast growth factor-21 (FGF-21) and peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) levels in rats fed with high fructose</atitle><jtitle>Molecular biology reports</jtitle><stitle>Mol Biol Rep</stitle><addtitle>Mol Biol Rep</addtitle><date>2023-06-01</date><risdate>2023</risdate><volume>50</volume><issue>6</issue><spage>4983</spage><epage>4997</epage><pages>4983-4997</pages><issn>0301-4851</issn><eissn>1573-4978</eissn><abstract>Background
Available studies show that quercetin reduces Metabolic Syndrome (MetS) and its complications, increases insulin sensitivity and improves glucose levels. It has been reported that the increase in hepatic gene expressions of fibroblast growth factor-21 (FGF-21), an important metabolic regulator of insulin sensitivity, glucose and energy homeostasis, and peroxisome proliferator-activated receptor gamma coactivator-1α (PGC-1α), which plays a central role in the regulation of cellular energy metabolism, eliminate the negative effects of fructose in fructose-fed rats. The main purpose of our study is to examine the effects of quercetin on hepatic FGF-21 and PGC-1α expressions and levels, as well as its protective and therapeutic role on MetS components in rats fed with fructose.
Methods and results
In our study, 24 Sprague Dawley male rats were divided into 4 groups: control, fructose, quercetin, fructose+quercetin (
n
= 6). During the 10-week experiment, quercetin was administered at a daily dose of 15 mg/kg body weight and fructose at a rate of 20%. Blood pressure and weights of all groups were measured and recorded. At the end of week 10, blood and liver tissue samples were taken. Serum insulin, glucose and triglyceride, total, HDL and VLDL cholesterol levels were determined from the samples. Insulin resistance was calculated using the HOMA-IR formula. Hepatic PGC-1α and FGF-21 protein levels and their mRNA expressions were determined. Criteria for metabolic syndrome were successfully established with fructose. It was observed that the administration of quercetin alone and in combination with fructose exerted positive effects and improved MetS criteria. It was determined that the administration of quercetin increased hepatic FGF-21 and PGC-1α protein levels and Messenger RNA (mRNA) expressions of them, which were decreased by fructose application.
Conclusions
The results of our study showed that 10-week administration of quercetin at 15 mg/kg exerted beneficial effects on lipid and carbohydrate metabolism in the fructose-mediated MetS model; therefore, quercetin may have great potential in the prevention and treatment of metabolic disorders.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>37086297</pmid><doi>10.1007/s11033-023-08444-y</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-2884-4753</orcidid><orcidid>https://orcid.org/0000-0002-5749-5687</orcidid><orcidid>https://orcid.org/0000-0002-0629-034X</orcidid><orcidid>https://orcid.org/0000-0002-8945-3801</orcidid><orcidid>https://orcid.org/0000-0002-6799-6522</orcidid></addata></record> |
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subjects | Animal Anatomy Animal Biochemistry Animals Biomedical and Life Sciences Blood pressure blood serum Body weight Carbohydrate metabolism Cholesterol energy Energy balance Energy metabolism Fibroblast growth factors Fibroblast Growth Factors - metabolism Fibroblasts Fructose Fructose - metabolism Fructose - pharmacology genes Glucose Glucose - metabolism Growth factors High density lipoprotein Histology Homeostasis insulin Insulin Resistance Life Sciences Lipid metabolism Lipoproteins (very low density) Liver Liver - metabolism Male males messenger RNA Metabolic disorders Metabolic syndrome Metabolic Syndrome - metabolism Morphology mRNA Original Article peroxisome proliferator-activated receptor gamma Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - genetics Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - metabolism Peroxisome proliferator-activated receptors Quercetin Quercetin - metabolism Quercetin - pharmacology Rats Rats, Sprague-Dawley RNA, Messenger - metabolism therapeutics triacylglycerols very low density lipoprotein |
title | Effects of quercetin on hepatic fibroblast growth factor-21 (FGF-21) and peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) levels in rats fed with high fructose |
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