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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Veröffentlicht in:Molecular biology reports 2023-06, Vol.50 (6), p.4983-4997
Hauptverfasser: Kocaman Kalkan, Kardelen, Şen, Serkan, Narlı, Belkıs, Seymen, Cemile Merve, Yılmaz, Canan
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container_title Molecular biology reports
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Şen, Serkan
Narlı, Belkıs
Seymen, Cemile Merve
Yılmaz, Canan
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
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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. 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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. 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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 - 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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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source MEDLINE; SpringerLink Journals - AutoHoldings
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T13%3A11%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effects%20of%20quercetin%20on%20hepatic%20fibroblast%20growth%20factor-21%20(FGF-21)%20and%20peroxisome%20proliferator-activated%20receptor%20gamma%20coactivator%201-alpha%20(PGC-1%CE%B1)%20levels%20in%20rats%20fed%20with%20high%20fructose&rft.jtitle=Molecular%20biology%20reports&rft.au=Kocaman%20Kalkan,%20Kardelen&rft.date=2023-06-01&rft.volume=50&rft.issue=6&rft.spage=4983&rft.epage=4997&rft.pages=4983-4997&rft.issn=0301-4851&rft.eissn=1573-4978&rft_id=info:doi/10.1007/s11033-023-08444-y&rft_dat=%3Cproquest_cross%3E2805028716%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2818550431&rft_id=info:pmid/37086297&rfr_iscdi=true