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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...
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Published in: | Nutrients 2019-01, Vol.11 (1), p.153 |
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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 & 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 & 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 & 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 & 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 & Medical Complete (Alumni)</collection><collection>Health & 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 |
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