Cocoa ameliorates renal injury in Zucker diabetic fatty rats by preventing oxidative stress, apoptosis and inactivation of autophagy
Redox balance, autophagy and apoptosis are main processes involved in the development of diabetic nephropathy. Epidemiological and animal studies suggest that cocoa might reduce the risk of diabetic complications. However, the molecular mechanisms responsible for these potential preventive activitie...
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description | Redox balance, autophagy and apoptosis are main processes involved in the development of diabetic nephropathy. Epidemiological and animal studies suggest that cocoa might reduce the risk of diabetic complications. However, the molecular mechanisms responsible for these potential preventive activities and whether cocoa exerts beneficial effects on dysregulated signalling pathways involved in cellular antioxidant defence, autophagy and apoptosis in the diabetic kidney remain largely unknown. Therefore, this work investigated the effect of a cocoa-rich diet on the mentioned processes in the renal cortex of Zucker Diabetic Fatty (ZDF) rats. Male ZDF rats were fed either a control or cocoa-rich diet (10%), and Zucker lean animals received the control diet (10-20 weeks-of-life). ZDF rats fed with cocoa decreased body weight and glucose and insulin levels, and improved renal function. Cocoa intake further prevented the enhanced renal cortical oxidative stress in diabetic rats by regulating the antioxidant defence system and close-related proteins to cytoprotection and cell response; thus, cocoa diminished oxidative markers (reactive oxygen species and carbonyl groups) and NADPH-oxidase-4 levels, and restored key enzymatic antioxidant activities (superoxide dismutase and catalase), nuclear-erythroid-2-related factor-2, and ERK-MAPK levels, as well as sirtuin-1/5′-AMP-activated-protein kinase signalling. Moreover, in ZDF rats cocoa-rich diet contributed to alleviation of the renal cortical injury through autophagy activation (p62 upregulation, and downregulation of beclin-1 and LC3), and inhibition of apoptosis (Bcl-x
L
stimulation and suppression of Bax and caspases-9 and -3). These findings provide the first
in vivo
evidence on the molecular mechanisms of cocoa to circumvent renal cortical damage that involve improvement of antioxidant competences, stimulation of autophagy and suppression of apoptosis in ZDF rats.
Cocoa prevents main processes involved in the development of diabetic nephropathy including redox imbalance, apoptosis and inhibition of autophagy. |
doi_str_mv | 10.1039/c9fo01806a |
format | Article |
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L
stimulation and suppression of Bax and caspases-9 and -3). These findings provide the first
in vivo
evidence on the molecular mechanisms of cocoa to circumvent renal cortical damage that involve improvement of antioxidant competences, stimulation of autophagy and suppression of apoptosis in ZDF rats.
Cocoa prevents main processes involved in the development of diabetic nephropathy including redox imbalance, apoptosis and inhibition of autophagy.</description><identifier>ISSN: 2042-6496</identifier><identifier>EISSN: 2042-650X</identifier><identifier>DOI: 10.1039/c9fo01806a</identifier><identifier>PMID: 31773121</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>AMP ; Animals ; Antioxidants ; Apoptosis ; Apoptosis - drug effects ; Autophagy ; Autophagy - drug effects ; Bax protein ; Bcl-x protein ; Beclin-1 - genetics ; Beclin-1 - metabolism ; Blood Glucose - metabolism ; Body weight ; Cacao - chemistry ; Carbonyl compounds ; Carbonyl groups ; Carbonyls ; Catalase ; Catalase - genetics ; Catalase - metabolism ; Cocoa ; Complications ; Deactivation ; Diabetes ; Diabetes mellitus ; Diabetes Mellitus - drug therapy ; Diabetes Mellitus - genetics ; Diabetes Mellitus - metabolism ; Diabetes Mellitus - physiopathology ; Diet ; Epidemiology ; Extracellular signal-regulated kinase ; Humans ; Inactivation ; Injury prevention ; Insulin ; Insulin - metabolism ; Kidney - drug effects ; Kidney - metabolism ; Kinases ; Male ; MAP kinase ; Molecular modelling ; NAD(P)H oxidase ; Nephropathy ; NF-E2-Related Factor 2 - genetics ; NF-E2-Related Factor 2 - metabolism ; Oxidative stress ; Oxidative Stress - drug effects ; Phagocytosis ; Protein kinase ; Proteins ; Rats ; Rats, Zucker ; Reactive oxygen species ; Renal function ; Risk reduction ; Rodents ; Signal transduction ; Signaling ; Stimulation ; Superoxide dismutase ; Superoxide Dismutase - genetics ; Superoxide Dismutase - metabolism</subject><ispartof>Food & function, 2019-12, Vol.1 (12), p.7926-7939</ispartof><rights>Copyright Royal Society of Chemistry 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c440t-d849ff02093aeb09b97cc239e9d82ab3b74776de615665b34e53cb6973994c3</citedby><cites>FETCH-LOGICAL-c440t-d849ff02093aeb09b97cc239e9d82ab3b74776de615665b34e53cb6973994c3</cites><orcidid>0000-0003-2649-2616</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31773121$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Álvarez-Cilleros, David</creatorcontrib><creatorcontrib>López-Oliva, María Elvira</creatorcontrib><creatorcontrib>Martín, María Ángeles</creatorcontrib><creatorcontrib>Ramos, Sonia</creatorcontrib><title>Cocoa ameliorates renal injury in Zucker diabetic fatty rats by preventing oxidative stress, apoptosis and inactivation of autophagy</title><title>Food & function</title><addtitle>Food Funct</addtitle><description>Redox balance, autophagy and apoptosis are main processes involved in the development of diabetic nephropathy. Epidemiological and animal studies suggest that cocoa might reduce the risk of diabetic complications. However, the molecular mechanisms responsible for these potential preventive activities and whether cocoa exerts beneficial effects on dysregulated signalling pathways involved in cellular antioxidant defence, autophagy and apoptosis in the diabetic kidney remain largely unknown. Therefore, this work investigated the effect of a cocoa-rich diet on the mentioned processes in the renal cortex of Zucker Diabetic Fatty (ZDF) rats. Male ZDF rats were fed either a control or cocoa-rich diet (10%), and Zucker lean animals received the control diet (10-20 weeks-of-life). ZDF rats fed with cocoa decreased body weight and glucose and insulin levels, and improved renal function. Cocoa intake further prevented the enhanced renal cortical oxidative stress in diabetic rats by regulating the antioxidant defence system and close-related proteins to cytoprotection and cell response; thus, cocoa diminished oxidative markers (reactive oxygen species and carbonyl groups) and NADPH-oxidase-4 levels, and restored key enzymatic antioxidant activities (superoxide dismutase and catalase), nuclear-erythroid-2-related factor-2, and ERK-MAPK levels, as well as sirtuin-1/5′-AMP-activated-protein kinase signalling. Moreover, in ZDF rats cocoa-rich diet contributed to alleviation of the renal cortical injury through autophagy activation (p62 upregulation, and downregulation of beclin-1 and LC3), and inhibition of apoptosis (Bcl-x
L
stimulation and suppression of Bax and caspases-9 and -3). These findings provide the first
in vivo
evidence on the molecular mechanisms of cocoa to circumvent renal cortical damage that involve improvement of antioxidant competences, stimulation of autophagy and suppression of apoptosis in ZDF rats.
Cocoa prevents main processes involved in the development of diabetic nephropathy including redox imbalance, apoptosis and inhibition of autophagy.</description><subject>AMP</subject><subject>Animals</subject><subject>Antioxidants</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Autophagy</subject><subject>Autophagy - drug effects</subject><subject>Bax protein</subject><subject>Bcl-x protein</subject><subject>Beclin-1 - genetics</subject><subject>Beclin-1 - metabolism</subject><subject>Blood Glucose - metabolism</subject><subject>Body weight</subject><subject>Cacao - chemistry</subject><subject>Carbonyl compounds</subject><subject>Carbonyl groups</subject><subject>Carbonyls</subject><subject>Catalase</subject><subject>Catalase - genetics</subject><subject>Catalase - metabolism</subject><subject>Cocoa</subject><subject>Complications</subject><subject>Deactivation</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetes Mellitus - drug therapy</subject><subject>Diabetes Mellitus - genetics</subject><subject>Diabetes Mellitus - metabolism</subject><subject>Diabetes Mellitus - physiopathology</subject><subject>Diet</subject><subject>Epidemiology</subject><subject>Extracellular signal-regulated kinase</subject><subject>Humans</subject><subject>Inactivation</subject><subject>Injury prevention</subject><subject>Insulin</subject><subject>Insulin - metabolism</subject><subject>Kidney - drug effects</subject><subject>Kidney - metabolism</subject><subject>Kinases</subject><subject>Male</subject><subject>MAP kinase</subject><subject>Molecular modelling</subject><subject>NAD(P)H oxidase</subject><subject>Nephropathy</subject><subject>NF-E2-Related Factor 2 - genetics</subject><subject>NF-E2-Related Factor 2 - metabolism</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Phagocytosis</subject><subject>Protein kinase</subject><subject>Proteins</subject><subject>Rats</subject><subject>Rats, Zucker</subject><subject>Reactive oxygen species</subject><subject>Renal function</subject><subject>Risk reduction</subject><subject>Rodents</subject><subject>Signal transduction</subject><subject>Signaling</subject><subject>Stimulation</subject><subject>Superoxide dismutase</subject><subject>Superoxide Dismutase - genetics</subject><subject>Superoxide Dismutase - metabolism</subject><issn>2042-6496</issn><issn>2042-650X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90c9rFTEQB_BQlLbUXry3RHoR8Wl-vezmWB62CoUe9CBelkl2ts3rvs02yRb37h_e1Ncf4MFcJjAfBma-hLzl7BNn0nx2pguM10zDDtkXTImFXrKfr57-yug9cpjSmpUnjalNvUv2JK8qyQXfJ39WwQWgsMHehwgZE404QE_9sJ7iXAr9NbkbjLT1YDF7RzvIeabFJmpnOka8wyH74YqG376F7O-QphwxpY8UxjDmkHyiMLRlFrjSLiQMNHQUphzGa7ia35DXHfQJDx_rAfl-9uXH6uvi4vL82-r0YuGUYnnR1sp0HRPMSEDLjDWVc0IaNG0twEpbqarSLWq-1HpppcKldFabquytnDwg77dTxxhuJ0y52fjksO9hwDClRkhuuFFKiEJP_qHrMMVylgclVLm2FrqoD1vlYkgpYteM0W8gzg1nzUM4zcqcXf4N57Tg48eRk91g-0yfoijg3RbE5J67L-k2Y9sVc_Q_I-8B3xmgtQ</recordid><startdate>20191211</startdate><enddate>20191211</enddate><creator>Álvarez-Cilleros, David</creator><creator>López-Oliva, María Elvira</creator><creator>Martín, María Ángeles</creator><creator>Ramos, Sonia</creator><general>Royal Society of Chemistry</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>7T5</scope><scope>7T7</scope><scope>7TO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2649-2616</orcidid></search><sort><creationdate>20191211</creationdate><title>Cocoa ameliorates renal injury in Zucker diabetic fatty rats by preventing oxidative stress, apoptosis and inactivation of autophagy</title><author>Álvarez-Cilleros, David ; López-Oliva, María Elvira ; Martín, María Ángeles ; Ramos, Sonia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-d849ff02093aeb09b97cc239e9d82ab3b74776de615665b34e53cb6973994c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>AMP</topic><topic>Animals</topic><topic>Antioxidants</topic><topic>Apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Autophagy</topic><topic>Autophagy - drug effects</topic><topic>Bax protein</topic><topic>Bcl-x protein</topic><topic>Beclin-1 - genetics</topic><topic>Beclin-1 - metabolism</topic><topic>Blood Glucose - metabolism</topic><topic>Body weight</topic><topic>Cacao - chemistry</topic><topic>Carbonyl compounds</topic><topic>Carbonyl groups</topic><topic>Carbonyls</topic><topic>Catalase</topic><topic>Catalase - genetics</topic><topic>Catalase - metabolism</topic><topic>Cocoa</topic><topic>Complications</topic><topic>Deactivation</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetes Mellitus - drug therapy</topic><topic>Diabetes Mellitus - genetics</topic><topic>Diabetes Mellitus - metabolism</topic><topic>Diabetes Mellitus - physiopathology</topic><topic>Diet</topic><topic>Epidemiology</topic><topic>Extracellular signal-regulated kinase</topic><topic>Humans</topic><topic>Inactivation</topic><topic>Injury prevention</topic><topic>Insulin</topic><topic>Insulin - metabolism</topic><topic>Kidney - drug effects</topic><topic>Kidney - metabolism</topic><topic>Kinases</topic><topic>Male</topic><topic>MAP kinase</topic><topic>Molecular modelling</topic><topic>NAD(P)H oxidase</topic><topic>Nephropathy</topic><topic>NF-E2-Related Factor 2 - genetics</topic><topic>NF-E2-Related Factor 2 - metabolism</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Phagocytosis</topic><topic>Protein kinase</topic><topic>Proteins</topic><topic>Rats</topic><topic>Rats, Zucker</topic><topic>Reactive oxygen species</topic><topic>Renal function</topic><topic>Risk reduction</topic><topic>Rodents</topic><topic>Signal transduction</topic><topic>Signaling</topic><topic>Stimulation</topic><topic>Superoxide dismutase</topic><topic>Superoxide Dismutase - genetics</topic><topic>Superoxide Dismutase - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Álvarez-Cilleros, David</creatorcontrib><creatorcontrib>López-Oliva, María Elvira</creatorcontrib><creatorcontrib>Martín, María Ángeles</creatorcontrib><creatorcontrib>Ramos, Sonia</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Food & function</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Álvarez-Cilleros, David</au><au>López-Oliva, María Elvira</au><au>Martín, María Ángeles</au><au>Ramos, Sonia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cocoa ameliorates renal injury in Zucker diabetic fatty rats by preventing oxidative stress, apoptosis and inactivation of autophagy</atitle><jtitle>Food & function</jtitle><addtitle>Food Funct</addtitle><date>2019-12-11</date><risdate>2019</risdate><volume>1</volume><issue>12</issue><spage>7926</spage><epage>7939</epage><pages>7926-7939</pages><issn>2042-6496</issn><eissn>2042-650X</eissn><abstract>Redox balance, autophagy and apoptosis are main processes involved in the development of diabetic nephropathy. Epidemiological and animal studies suggest that cocoa might reduce the risk of diabetic complications. However, the molecular mechanisms responsible for these potential preventive activities and whether cocoa exerts beneficial effects on dysregulated signalling pathways involved in cellular antioxidant defence, autophagy and apoptosis in the diabetic kidney remain largely unknown. Therefore, this work investigated the effect of a cocoa-rich diet on the mentioned processes in the renal cortex of Zucker Diabetic Fatty (ZDF) rats. Male ZDF rats were fed either a control or cocoa-rich diet (10%), and Zucker lean animals received the control diet (10-20 weeks-of-life). ZDF rats fed with cocoa decreased body weight and glucose and insulin levels, and improved renal function. Cocoa intake further prevented the enhanced renal cortical oxidative stress in diabetic rats by regulating the antioxidant defence system and close-related proteins to cytoprotection and cell response; thus, cocoa diminished oxidative markers (reactive oxygen species and carbonyl groups) and NADPH-oxidase-4 levels, and restored key enzymatic antioxidant activities (superoxide dismutase and catalase), nuclear-erythroid-2-related factor-2, and ERK-MAPK levels, as well as sirtuin-1/5′-AMP-activated-protein kinase signalling. Moreover, in ZDF rats cocoa-rich diet contributed to alleviation of the renal cortical injury through autophagy activation (p62 upregulation, and downregulation of beclin-1 and LC3), and inhibition of apoptosis (Bcl-x
L
stimulation and suppression of Bax and caspases-9 and -3). These findings provide the first
in vivo
evidence on the molecular mechanisms of cocoa to circumvent renal cortical damage that involve improvement of antioxidant competences, stimulation of autophagy and suppression of apoptosis in ZDF rats.
Cocoa prevents main processes involved in the development of diabetic nephropathy including redox imbalance, apoptosis and inhibition of autophagy.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>31773121</pmid><doi>10.1039/c9fo01806a</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-2649-2616</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | AMP Animals Antioxidants Apoptosis Apoptosis - drug effects Autophagy Autophagy - drug effects Bax protein Bcl-x protein Beclin-1 - genetics Beclin-1 - metabolism Blood Glucose - metabolism Body weight Cacao - chemistry Carbonyl compounds Carbonyl groups Carbonyls Catalase Catalase - genetics Catalase - metabolism Cocoa Complications Deactivation Diabetes Diabetes mellitus Diabetes Mellitus - drug therapy Diabetes Mellitus - genetics Diabetes Mellitus - metabolism Diabetes Mellitus - physiopathology Diet Epidemiology Extracellular signal-regulated kinase Humans Inactivation Injury prevention Insulin Insulin - metabolism Kidney - drug effects Kidney - metabolism Kinases Male MAP kinase Molecular modelling NAD(P)H oxidase Nephropathy NF-E2-Related Factor 2 - genetics NF-E2-Related Factor 2 - metabolism Oxidative stress Oxidative Stress - drug effects Phagocytosis Protein kinase Proteins Rats Rats, Zucker Reactive oxygen species Renal function Risk reduction Rodents Signal transduction Signaling Stimulation Superoxide dismutase Superoxide Dismutase - genetics Superoxide Dismutase - metabolism |
title | Cocoa ameliorates renal injury in Zucker diabetic fatty rats by preventing oxidative stress, apoptosis and inactivation of autophagy |
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