Loading…

Beneficial Effects of an Aged Black Garlic Extract in the Metabolic and Vascular Alterations Induced by a High Fat/Sucrose Diet in Male Rats

Aged black garlic (ABG) is a functional food with antioxidant and anti-inflammatory properties. Recent studies also report its beneficial metabolic effects in a context of obesity or diabetes, although the mechanisms involved are poorly understood. The aim of this work was to analyze the effects of...

Full description

Saved in:
Bibliographic Details
Published in:Nutrients 2019-01, Vol.11 (1), p.153
Main Authors: Amor, Sara, González-Hedström, Daniel, Martín-Carro, Beatriz, Inarejos-García, Antonio Manuel, Almodóvar, Paula, Prodanov, Marin, García-Villalón, Angel Luis, Granado, Miriam
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c439t-63f28b25c5901a8af1588995882a637656417b061a621580fa2c8bbdf1b614cb3
cites cdi_FETCH-LOGICAL-c439t-63f28b25c5901a8af1588995882a637656417b061a621580fa2c8bbdf1b614cb3
container_end_page
container_issue 1
container_start_page 153
container_title Nutrients
container_volume 11
creator Amor, Sara
González-Hedström, Daniel
Martín-Carro, Beatriz
Inarejos-García, Antonio Manuel
Almodóvar, Paula
Prodanov, Marin
García-Villalón, Angel Luis
Granado, Miriam
description Aged black garlic (ABG) is a functional food with antioxidant and anti-inflammatory properties. Recent studies also report its beneficial metabolic effects in a context of obesity or diabetes, although the mechanisms involved are poorly understood. The aim of this work was to analyze the effects of an ABG extract in the vascular and metabolic alterations induced by a high-fat/sucrose diet in rats. For this purpose, male Sprague⁻Dawley rats were fed either a standard chow (controls; = 12) or a high-fat/sucrose diet (HFD; = 24) for 16 weeks. From week 8 on, half of the HFD rats were treated with a commercial ABG extract concentrated in S-allyl cysteine and melanoidins (ABG10+®; 250 mg/kg daily by gavage; 5 mL/kg). ABG10+®-treated rats showed lower mean caloric intake, body weight, triglycerides, low density lipoprotein cholesterol (LDL-c), insulin and leptin serum concentrations and higher high density lipoprotein cholesterol (HDL-c) and adiponectin serum concentrations than non-treated rats. In the hypothalamus, ABG10+® treatment induced an increase in the gene expression of proopiomelanocortin ( ) and a decrease in leptin receptor ( ) mRNA levels. No significant changes were found in visceral adipose tissue except for an overexpression of β3-adrenergic receptor ( ) in ABG-treated rats. In subcutaneous adipose tissue, ABG10+® treatment decreased adipose weight and downregulated the gene expression of , , and . In brown adipose tissue, an overexpression of , , and in ABG10+®-treated rats was found, whereas PPAR-γ mRNA levels were significantly decreased. Regarding vascular function, ABG10+® treatment attenuated the obesity-induced vasoconstriction in response to potassium chloride both in presence/absence of perivascular adipose tissue (PVAT). On the contrary, aorta segments from ABG-treated rats showed and improved relaxation in response to acetylcholine only when PVAT was present, with this fact possible being related to the decreased gene expression of proinflammatory cytokines in this tissue. In conclusion, ABG10+® administration partially improves the metabolic and vascular alterations induced by a high-fat/high-sucrose diet in rats through modifications in the gene expression of proteins and neuropeptides involved in inflammation, fat metabolism and food intake regulation. Further studies are required to assess the bioavailability of ABG between rats and humans.
doi_str_mv 10.3390/nu11010153
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6356877</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2302263860</sourcerecordid><originalsourceid>FETCH-LOGICAL-c439t-63f28b25c5901a8af1588995882a637656417b061a621580fa2c8bbdf1b614cb3</originalsourceid><addsrcrecordid>eNqFkttqFTEUhgdRbKm98QEk4I0I2-Ywk8zcCLt19wAtgqfbsJJJ9k7NTtokI_YdfGgzttbqjQkkgf_nY62Vv2meE_yGsQEfhIkQXHfHHjW7FAu64Lxljx-8d5r9nC_xvAQWnD1tdhjmLcWM7TY_Dk0w1mkHHq2sNbpkFC2CgJZrM6JDD_orOoHknUar7yWBLsgFVDYGXZgCKs4ChBF9gawnDwktfTEJiosho7MwTrpi1A0CdOrWG3QM5eDjpFPMBr1z5hfsArxBH6DkZ80TCz6b_bt7r_l8vPp0dLo4f39ydrQ8X-iWDWXBmaW9op3uBkygB0u6vh-GelDgTPCOt0QozAlwWiVsgepeqdESxUmrFdtr3t5yrya1NaM2oTbm5VVyW0g3MoKTfyvBbeQ6fpOcdbwXogJe3QFSvJ5MLnLrsjbeQzBxypLSng-YC8r-byViqB9Jhpn68h_rZZxSqJOQlGFKOes5rq7Xt655iDkZe183wXKOhPwTiWp-8bDTe-vvALCfg0OvKA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2302263860</pqid></control><display><type>article</type><title>Beneficial Effects of an Aged Black Garlic Extract in the Metabolic and Vascular Alterations Induced by a High Fat/Sucrose Diet in Male Rats</title><source>Publicly Available Content (ProQuest)</source><source>PubMed Central</source><creator>Amor, Sara ; González-Hedström, Daniel ; Martín-Carro, Beatriz ; Inarejos-García, Antonio Manuel ; Almodóvar, Paula ; Prodanov, Marin ; García-Villalón, Angel Luis ; Granado, Miriam</creator><creatorcontrib>Amor, Sara ; González-Hedström, Daniel ; Martín-Carro, Beatriz ; Inarejos-García, Antonio Manuel ; Almodóvar, Paula ; Prodanov, Marin ; García-Villalón, Angel Luis ; Granado, Miriam</creatorcontrib><description>Aged black garlic (ABG) is a functional food with antioxidant and anti-inflammatory properties. Recent studies also report its beneficial metabolic effects in a context of obesity or diabetes, although the mechanisms involved are poorly understood. The aim of this work was to analyze the effects of an ABG extract in the vascular and metabolic alterations induced by a high-fat/sucrose diet in rats. For this purpose, male Sprague⁻Dawley rats were fed either a standard chow (controls; = 12) or a high-fat/sucrose diet (HFD; = 24) for 16 weeks. From week 8 on, half of the HFD rats were treated with a commercial ABG extract concentrated in S-allyl cysteine and melanoidins (ABG10+®; 250 mg/kg daily by gavage; 5 mL/kg). ABG10+®-treated rats showed lower mean caloric intake, body weight, triglycerides, low density lipoprotein cholesterol (LDL-c), insulin and leptin serum concentrations and higher high density lipoprotein cholesterol (HDL-c) and adiponectin serum concentrations than non-treated rats. In the hypothalamus, ABG10+® treatment induced an increase in the gene expression of proopiomelanocortin ( ) and a decrease in leptin receptor ( ) mRNA levels. No significant changes were found in visceral adipose tissue except for an overexpression of β3-adrenergic receptor ( ) in ABG-treated rats. In subcutaneous adipose tissue, ABG10+® treatment decreased adipose weight and downregulated the gene expression of , , and . In brown adipose tissue, an overexpression of , , and in ABG10+®-treated rats was found, whereas PPAR-γ mRNA levels were significantly decreased. Regarding vascular function, ABG10+® treatment attenuated the obesity-induced vasoconstriction in response to potassium chloride both in presence/absence of perivascular adipose tissue (PVAT). On the contrary, aorta segments from ABG-treated rats showed and improved relaxation in response to acetylcholine only when PVAT was present, with this fact possible being related to the decreased gene expression of proinflammatory cytokines in this tissue. In conclusion, ABG10+® administration partially improves the metabolic and vascular alterations induced by a high-fat/high-sucrose diet in rats through modifications in the gene expression of proteins and neuropeptides involved in inflammation, fat metabolism and food intake regulation. Further studies are required to assess the bioavailability of ABG between rats and humans.</description><identifier>ISSN: 2072-6643</identifier><identifier>EISSN: 2072-6643</identifier><identifier>DOI: 10.3390/nu11010153</identifier><identifier>PMID: 30642033</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Acetylcholine ; Adenylate cyclase ; Adipocytes ; adiponectin ; Adiponectin - blood ; Adipose tissue ; Adiposity - drug effects ; Adrenergic receptors ; Animals ; anti-inflammatory activity ; antioxidants ; Antioxidants - pharmacology ; aorta ; bioavailability ; blood serum ; Body Weight ; brown adipose tissue ; Cholesterol, HDL - blood ; Contraction ; cysteine ; cytokines ; Diabetes ; Diet, High-Fat - adverse effects ; Dietary Sucrose - administration &amp; dosage ; Energy balance ; energy intake ; Fat metabolism ; food intake ; functional foods ; Garlic ; Garlic - chemistry ; Gene expression ; Gene Expression Regulation ; gene overexpression ; Glucose Tolerance Test ; Glucose Transporter Type 4 - genetics ; Glucose Transporter Type 4 - metabolism ; Guanine ; high density lipoprotein cholesterol ; High fat diet ; Homeostasis ; Hypothalamus ; Hypothalamus - drug effects ; Inflammation ; Insulin ; Insulin - blood ; laboratory animals ; leptin ; Leptin - blood ; leptin receptors ; lipid metabolism ; Lipids ; Lipolysis ; low density lipoprotein cholesterol ; Male ; males ; Mass spectrometry ; melanoidins ; messenger RNA ; Metabolic syndrome ; Neuropeptides ; Nucleotides ; Obesity ; Organ Size - drug effects ; peroxisome proliferator-activated receptor gamma ; Plant Extracts - pharmacology ; Potassium chloride ; PPAR gamma - genetics ; PPAR gamma - metabolism ; pro-opiomelanocortin ; Rats ; Rats, Sprague-Dawley ; Receptor, Insulin - genetics ; Receptor, Insulin - metabolism ; Receptors, Adrenergic, beta-3 - genetics ; Receptors, Adrenergic, beta-3 - metabolism ; Scientific imaging ; Sensors ; Sucrose ; Sugar ; Sympathomimetics ; triacylglycerols ; Triglycerides - blood ; Uncoupling Protein 1 - genetics ; Uncoupling Protein 1 - metabolism ; vasoconstriction</subject><ispartof>Nutrients, 2019-01, Vol.11 (1), p.153</ispartof><rights>2019. This work is licensed under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 by the authors. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-63f28b25c5901a8af1588995882a637656417b061a621580fa2c8bbdf1b614cb3</citedby><cites>FETCH-LOGICAL-c439t-63f28b25c5901a8af1588995882a637656417b061a621580fa2c8bbdf1b614cb3</cites><orcidid>0000-0001-9178-8822 ; 0000-0002-4869-6188</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2302263860/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2302263860?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30642033$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Amor, Sara</creatorcontrib><creatorcontrib>González-Hedström, Daniel</creatorcontrib><creatorcontrib>Martín-Carro, Beatriz</creatorcontrib><creatorcontrib>Inarejos-García, Antonio Manuel</creatorcontrib><creatorcontrib>Almodóvar, Paula</creatorcontrib><creatorcontrib>Prodanov, Marin</creatorcontrib><creatorcontrib>García-Villalón, Angel Luis</creatorcontrib><creatorcontrib>Granado, Miriam</creatorcontrib><title>Beneficial Effects of an Aged Black Garlic Extract in the Metabolic and Vascular Alterations Induced by a High Fat/Sucrose Diet in Male Rats</title><title>Nutrients</title><addtitle>Nutrients</addtitle><description>Aged black garlic (ABG) is a functional food with antioxidant and anti-inflammatory properties. Recent studies also report its beneficial metabolic effects in a context of obesity or diabetes, although the mechanisms involved are poorly understood. The aim of this work was to analyze the effects of an ABG extract in the vascular and metabolic alterations induced by a high-fat/sucrose diet in rats. For this purpose, male Sprague⁻Dawley rats were fed either a standard chow (controls; = 12) or a high-fat/sucrose diet (HFD; = 24) for 16 weeks. From week 8 on, half of the HFD rats were treated with a commercial ABG extract concentrated in S-allyl cysteine and melanoidins (ABG10+®; 250 mg/kg daily by gavage; 5 mL/kg). ABG10+®-treated rats showed lower mean caloric intake, body weight, triglycerides, low density lipoprotein cholesterol (LDL-c), insulin and leptin serum concentrations and higher high density lipoprotein cholesterol (HDL-c) and adiponectin serum concentrations than non-treated rats. In the hypothalamus, ABG10+® treatment induced an increase in the gene expression of proopiomelanocortin ( ) and a decrease in leptin receptor ( ) mRNA levels. No significant changes were found in visceral adipose tissue except for an overexpression of β3-adrenergic receptor ( ) in ABG-treated rats. In subcutaneous adipose tissue, ABG10+® treatment decreased adipose weight and downregulated the gene expression of , , and . In brown adipose tissue, an overexpression of , , and in ABG10+®-treated rats was found, whereas PPAR-γ mRNA levels were significantly decreased. Regarding vascular function, ABG10+® treatment attenuated the obesity-induced vasoconstriction in response to potassium chloride both in presence/absence of perivascular adipose tissue (PVAT). On the contrary, aorta segments from ABG-treated rats showed and improved relaxation in response to acetylcholine only when PVAT was present, with this fact possible being related to the decreased gene expression of proinflammatory cytokines in this tissue. In conclusion, ABG10+® administration partially improves the metabolic and vascular alterations induced by a high-fat/high-sucrose diet in rats through modifications in the gene expression of proteins and neuropeptides involved in inflammation, fat metabolism and food intake regulation. Further studies are required to assess the bioavailability of ABG between rats and humans.</description><subject>Acetylcholine</subject><subject>Adenylate cyclase</subject><subject>Adipocytes</subject><subject>adiponectin</subject><subject>Adiponectin - blood</subject><subject>Adipose tissue</subject><subject>Adiposity - drug effects</subject><subject>Adrenergic receptors</subject><subject>Animals</subject><subject>anti-inflammatory activity</subject><subject>antioxidants</subject><subject>Antioxidants - pharmacology</subject><subject>aorta</subject><subject>bioavailability</subject><subject>blood serum</subject><subject>Body Weight</subject><subject>brown adipose tissue</subject><subject>Cholesterol, HDL - blood</subject><subject>Contraction</subject><subject>cysteine</subject><subject>cytokines</subject><subject>Diabetes</subject><subject>Diet, High-Fat - adverse effects</subject><subject>Dietary Sucrose - administration &amp; dosage</subject><subject>Energy balance</subject><subject>energy intake</subject><subject>Fat metabolism</subject><subject>food intake</subject><subject>functional foods</subject><subject>Garlic</subject><subject>Garlic - chemistry</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>gene overexpression</subject><subject>Glucose Tolerance Test</subject><subject>Glucose Transporter Type 4 - genetics</subject><subject>Glucose Transporter Type 4 - metabolism</subject><subject>Guanine</subject><subject>high density lipoprotein cholesterol</subject><subject>High fat diet</subject><subject>Homeostasis</subject><subject>Hypothalamus</subject><subject>Hypothalamus - drug effects</subject><subject>Inflammation</subject><subject>Insulin</subject><subject>Insulin - blood</subject><subject>laboratory animals</subject><subject>leptin</subject><subject>Leptin - blood</subject><subject>leptin receptors</subject><subject>lipid metabolism</subject><subject>Lipids</subject><subject>Lipolysis</subject><subject>low density lipoprotein cholesterol</subject><subject>Male</subject><subject>males</subject><subject>Mass spectrometry</subject><subject>melanoidins</subject><subject>messenger RNA</subject><subject>Metabolic syndrome</subject><subject>Neuropeptides</subject><subject>Nucleotides</subject><subject>Obesity</subject><subject>Organ Size - drug effects</subject><subject>peroxisome proliferator-activated receptor gamma</subject><subject>Plant Extracts - pharmacology</subject><subject>Potassium chloride</subject><subject>PPAR gamma - genetics</subject><subject>PPAR gamma - metabolism</subject><subject>pro-opiomelanocortin</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptor, Insulin - genetics</subject><subject>Receptor, Insulin - metabolism</subject><subject>Receptors, Adrenergic, beta-3 - genetics</subject><subject>Receptors, Adrenergic, beta-3 - metabolism</subject><subject>Scientific imaging</subject><subject>Sensors</subject><subject>Sucrose</subject><subject>Sugar</subject><subject>Sympathomimetics</subject><subject>triacylglycerols</subject><subject>Triglycerides - blood</subject><subject>Uncoupling Protein 1 - genetics</subject><subject>Uncoupling Protein 1 - metabolism</subject><subject>vasoconstriction</subject><issn>2072-6643</issn><issn>2072-6643</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNqFkttqFTEUhgdRbKm98QEk4I0I2-Ywk8zcCLt19wAtgqfbsJJJ9k7NTtokI_YdfGgzttbqjQkkgf_nY62Vv2meE_yGsQEfhIkQXHfHHjW7FAu64Lxljx-8d5r9nC_xvAQWnD1tdhjmLcWM7TY_Dk0w1mkHHq2sNbpkFC2CgJZrM6JDD_orOoHknUar7yWBLsgFVDYGXZgCKs4ChBF9gawnDwktfTEJiosho7MwTrpi1A0CdOrWG3QM5eDjpFPMBr1z5hfsArxBH6DkZ80TCz6b_bt7r_l8vPp0dLo4f39ydrQ8X-iWDWXBmaW9op3uBkygB0u6vh-GelDgTPCOt0QozAlwWiVsgepeqdESxUmrFdtr3t5yrya1NaM2oTbm5VVyW0g3MoKTfyvBbeQ6fpOcdbwXogJe3QFSvJ5MLnLrsjbeQzBxypLSng-YC8r-byViqB9Jhpn68h_rZZxSqJOQlGFKOes5rq7Xt655iDkZe183wXKOhPwTiWp-8bDTe-vvALCfg0OvKA</recordid><startdate>20190112</startdate><enddate>20190112</enddate><creator>Amor, Sara</creator><creator>González-Hedström, Daniel</creator><creator>Martín-Carro, Beatriz</creator><creator>Inarejos-García, Antonio Manuel</creator><creator>Almodóvar, Paula</creator><creator>Prodanov, Marin</creator><creator>García-Villalón, Angel Luis</creator><creator>Granado, Miriam</creator><general>MDPI AG</general><general>MDPI</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>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9178-8822</orcidid><orcidid>https://orcid.org/0000-0002-4869-6188</orcidid></search><sort><creationdate>20190112</creationdate><title>Beneficial Effects of an Aged Black Garlic Extract in the Metabolic and Vascular Alterations Induced by a High Fat/Sucrose Diet in Male Rats</title><author>Amor, Sara ; González-Hedström, Daniel ; Martín-Carro, Beatriz ; Inarejos-García, Antonio Manuel ; Almodóvar, Paula ; Prodanov, Marin ; García-Villalón, Angel Luis ; Granado, Miriam</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-63f28b25c5901a8af1588995882a637656417b061a621580fa2c8bbdf1b614cb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Acetylcholine</topic><topic>Adenylate cyclase</topic><topic>Adipocytes</topic><topic>adiponectin</topic><topic>Adiponectin - blood</topic><topic>Adipose tissue</topic><topic>Adiposity - drug effects</topic><topic>Adrenergic receptors</topic><topic>Animals</topic><topic>anti-inflammatory activity</topic><topic>antioxidants</topic><topic>Antioxidants - pharmacology</topic><topic>aorta</topic><topic>bioavailability</topic><topic>blood serum</topic><topic>Body Weight</topic><topic>brown adipose tissue</topic><topic>Cholesterol, HDL - blood</topic><topic>Contraction</topic><topic>cysteine</topic><topic>cytokines</topic><topic>Diabetes</topic><topic>Diet, High-Fat - adverse effects</topic><topic>Dietary Sucrose - administration &amp; dosage</topic><topic>Energy balance</topic><topic>energy intake</topic><topic>Fat metabolism</topic><topic>food intake</topic><topic>functional foods</topic><topic>Garlic</topic><topic>Garlic - chemistry</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>gene overexpression</topic><topic>Glucose Tolerance Test</topic><topic>Glucose Transporter Type 4 - genetics</topic><topic>Glucose Transporter Type 4 - metabolism</topic><topic>Guanine</topic><topic>high density lipoprotein cholesterol</topic><topic>High fat diet</topic><topic>Homeostasis</topic><topic>Hypothalamus</topic><topic>Hypothalamus - drug effects</topic><topic>Inflammation</topic><topic>Insulin</topic><topic>Insulin - blood</topic><topic>laboratory animals</topic><topic>leptin</topic><topic>Leptin - blood</topic><topic>leptin receptors</topic><topic>lipid metabolism</topic><topic>Lipids</topic><topic>Lipolysis</topic><topic>low density lipoprotein cholesterol</topic><topic>Male</topic><topic>males</topic><topic>Mass spectrometry</topic><topic>melanoidins</topic><topic>messenger RNA</topic><topic>Metabolic syndrome</topic><topic>Neuropeptides</topic><topic>Nucleotides</topic><topic>Obesity</topic><topic>Organ Size - drug effects</topic><topic>peroxisome proliferator-activated receptor gamma</topic><topic>Plant Extracts - pharmacology</topic><topic>Potassium chloride</topic><topic>PPAR gamma - genetics</topic><topic>PPAR gamma - metabolism</topic><topic>pro-opiomelanocortin</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptor, Insulin - genetics</topic><topic>Receptor, Insulin - metabolism</topic><topic>Receptors, Adrenergic, beta-3 - genetics</topic><topic>Receptors, Adrenergic, beta-3 - metabolism</topic><topic>Scientific imaging</topic><topic>Sensors</topic><topic>Sucrose</topic><topic>Sugar</topic><topic>Sympathomimetics</topic><topic>triacylglycerols</topic><topic>Triglycerides - blood</topic><topic>Uncoupling Protein 1 - genetics</topic><topic>Uncoupling Protein 1 - metabolism</topic><topic>vasoconstriction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Amor, Sara</creatorcontrib><creatorcontrib>González-Hedström, Daniel</creatorcontrib><creatorcontrib>Martín-Carro, Beatriz</creatorcontrib><creatorcontrib>Inarejos-García, Antonio Manuel</creatorcontrib><creatorcontrib>Almodóvar, Paula</creatorcontrib><creatorcontrib>Prodanov, Marin</creatorcontrib><creatorcontrib>García-Villalón, Angel Luis</creatorcontrib><creatorcontrib>Granado, Miriam</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>Physical Education Index</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content (ProQuest)</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 China</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nutrients</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Amor, Sara</au><au>González-Hedström, Daniel</au><au>Martín-Carro, Beatriz</au><au>Inarejos-García, Antonio Manuel</au><au>Almodóvar, Paula</au><au>Prodanov, Marin</au><au>García-Villalón, Angel Luis</au><au>Granado, Miriam</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Beneficial Effects of an Aged Black Garlic Extract in the Metabolic and Vascular Alterations Induced by a High Fat/Sucrose Diet in Male Rats</atitle><jtitle>Nutrients</jtitle><addtitle>Nutrients</addtitle><date>2019-01-12</date><risdate>2019</risdate><volume>11</volume><issue>1</issue><spage>153</spage><pages>153-</pages><issn>2072-6643</issn><eissn>2072-6643</eissn><abstract>Aged black garlic (ABG) is a functional food with antioxidant and anti-inflammatory properties. Recent studies also report its beneficial metabolic effects in a context of obesity or diabetes, although the mechanisms involved are poorly understood. The aim of this work was to analyze the effects of an ABG extract in the vascular and metabolic alterations induced by a high-fat/sucrose diet in rats. For this purpose, male Sprague⁻Dawley rats were fed either a standard chow (controls; = 12) or a high-fat/sucrose diet (HFD; = 24) for 16 weeks. From week 8 on, half of the HFD rats were treated with a commercial ABG extract concentrated in S-allyl cysteine and melanoidins (ABG10+®; 250 mg/kg daily by gavage; 5 mL/kg). ABG10+®-treated rats showed lower mean caloric intake, body weight, triglycerides, low density lipoprotein cholesterol (LDL-c), insulin and leptin serum concentrations and higher high density lipoprotein cholesterol (HDL-c) and adiponectin serum concentrations than non-treated rats. In the hypothalamus, ABG10+® treatment induced an increase in the gene expression of proopiomelanocortin ( ) and a decrease in leptin receptor ( ) mRNA levels. No significant changes were found in visceral adipose tissue except for an overexpression of β3-adrenergic receptor ( ) in ABG-treated rats. In subcutaneous adipose tissue, ABG10+® treatment decreased adipose weight and downregulated the gene expression of , , and . In brown adipose tissue, an overexpression of , , and in ABG10+®-treated rats was found, whereas PPAR-γ mRNA levels were significantly decreased. Regarding vascular function, ABG10+® treatment attenuated the obesity-induced vasoconstriction in response to potassium chloride both in presence/absence of perivascular adipose tissue (PVAT). On the contrary, aorta segments from ABG-treated rats showed and improved relaxation in response to acetylcholine only when PVAT was present, with this fact possible being related to the decreased gene expression of proinflammatory cytokines in this tissue. In conclusion, ABG10+® administration partially improves the metabolic and vascular alterations induced by a high-fat/high-sucrose diet in rats through modifications in the gene expression of proteins and neuropeptides involved in inflammation, fat metabolism and food intake regulation. Further studies are required to assess the bioavailability of ABG between rats and humans.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>30642033</pmid><doi>10.3390/nu11010153</doi><orcidid>https://orcid.org/0000-0001-9178-8822</orcidid><orcidid>https://orcid.org/0000-0002-4869-6188</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2072-6643
ispartof Nutrients, 2019-01, Vol.11 (1), p.153
issn 2072-6643
2072-6643
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6356877
source Publicly Available Content (ProQuest); PubMed Central
subjects Acetylcholine
Adenylate cyclase
Adipocytes
adiponectin
Adiponectin - blood
Adipose tissue
Adiposity - drug effects
Adrenergic receptors
Animals
anti-inflammatory activity
antioxidants
Antioxidants - pharmacology
aorta
bioavailability
blood serum
Body Weight
brown adipose tissue
Cholesterol, HDL - blood
Contraction
cysteine
cytokines
Diabetes
Diet, High-Fat - adverse effects
Dietary Sucrose - administration & dosage
Energy balance
energy intake
Fat metabolism
food intake
functional foods
Garlic
Garlic - chemistry
Gene expression
Gene Expression Regulation
gene overexpression
Glucose Tolerance Test
Glucose Transporter Type 4 - genetics
Glucose Transporter Type 4 - metabolism
Guanine
high density lipoprotein cholesterol
High fat diet
Homeostasis
Hypothalamus
Hypothalamus - drug effects
Inflammation
Insulin
Insulin - blood
laboratory animals
leptin
Leptin - blood
leptin receptors
lipid metabolism
Lipids
Lipolysis
low density lipoprotein cholesterol
Male
males
Mass spectrometry
melanoidins
messenger RNA
Metabolic syndrome
Neuropeptides
Nucleotides
Obesity
Organ Size - drug effects
peroxisome proliferator-activated receptor gamma
Plant Extracts - pharmacology
Potassium chloride
PPAR gamma - genetics
PPAR gamma - metabolism
pro-opiomelanocortin
Rats
Rats, Sprague-Dawley
Receptor, Insulin - genetics
Receptor, Insulin - metabolism
Receptors, Adrenergic, beta-3 - genetics
Receptors, Adrenergic, beta-3 - metabolism
Scientific imaging
Sensors
Sucrose
Sugar
Sympathomimetics
triacylglycerols
Triglycerides - blood
Uncoupling Protein 1 - genetics
Uncoupling Protein 1 - metabolism
vasoconstriction
title Beneficial Effects of an Aged Black Garlic Extract in the Metabolic and Vascular Alterations Induced by a High Fat/Sucrose Diet in Male Rats
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T14%3A38%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Beneficial%20Effects%20of%20an%20Aged%20Black%20Garlic%20Extract%20in%20the%20Metabolic%20and%20Vascular%20Alterations%20Induced%20by%20a%20High%20Fat/Sucrose%20Diet%20in%20Male%20Rats&rft.jtitle=Nutrients&rft.au=Amor,%20Sara&rft.date=2019-01-12&rft.volume=11&rft.issue=1&rft.spage=153&rft.pages=153-&rft.issn=2072-6643&rft.eissn=2072-6643&rft_id=info:doi/10.3390/nu11010153&rft_dat=%3Cproquest_pubme%3E2302263860%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c439t-63f28b25c5901a8af1588995882a637656417b061a621580fa2c8bbdf1b614cb3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2302263860&rft_id=info:pmid/30642033&rfr_iscdi=true