Recent novel approaches to limit oxidative stress and inflammation in diabetic complications
Diabetes is considered a major burden on the healthcare system of Western and non‐Western societies with the disease reaching epidemic proportions globally. Diabetic patients are highly susceptible to developing micro‐ and macrovascular complications, which contribute significantly to morbidity and...
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Veröffentlicht in: | Clinical & translational immunology 2018, Vol.7 (4), p.e1016-n/a |
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description | Diabetes is considered a major burden on the healthcare system of Western and non‐Western societies with the disease reaching epidemic proportions globally. Diabetic patients are highly susceptible to developing micro‐ and macrovascular complications, which contribute significantly to morbidity and mortality rates. Over the past decade, a plethora of research has demonstrated that oxidative stress and inflammation are intricately linked and significant drivers of these diabetic complications. Thus, the focus now has been towards specific mechanism‐based strategies that can target both oxidative stress and inflammatory pathways to improve the outcome of disease burden. This review will focus on the mechanisms that drive these diabetic complications and the feasibility of emerging new therapies to combat oxidative stress and inflammation in the diabetic milieu.
Hyperglycaemia‐induced oxidative stress drives pro‐inflammatory pathways to mediate end‐organ injury resulting in diabetic micro‐ and macrovascular complications. Targeting these downstream pathways is offering new avenues for therapeutic interventions to limit these debilitating complications. |
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Hyperglycaemia‐induced oxidative stress drives pro‐inflammatory pathways to mediate end‐organ injury resulting in diabetic micro‐ and macrovascular complications. Targeting these downstream pathways is offering new avenues for therapeutic interventions to limit these debilitating complications.</description><identifier>ISSN: 2050-0068</identifier><identifier>EISSN: 2050-0068</identifier><identifier>DOI: 10.1002/cti2.1016</identifier><identifier>PMID: 29713471</identifier><language>eng</language><publisher>Australia: John Wiley & Sons, Inc</publisher><subject>Antioxidants ; Atherosclerosis ; Blood pressure ; Cardiomyopathy ; cardiovascular disease ; chronic kidney disease ; Clinical trials ; Diabetes ; Diabetes mellitus ; Diabetic retinopathy ; Drugs ; Enzymes ; Expenditures ; Hyperglycemia ; Inflammation ; Kinases ; Metabolism ; Mitochondria ; Morbidity ; Nitric oxide ; Oxidation ; Oxidative stress ; retinopathy ; Risk factors</subject><ispartof>Clinical & translational immunology, 2018, Vol.7 (4), p.e1016-n/a</ispartof><rights>2018 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Australasian Society for Immunology Inc.</rights><rights>2018. This work is published under http://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><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5096-e41cc58981bec09c82e680d413295efc9ab43c22b1966dcf0d6cbb8a718e2a063</citedby><cites>FETCH-LOGICAL-c5096-e41cc58981bec09c82e680d413295efc9ab43c22b1966dcf0d6cbb8a718e2a063</cites><orcidid>0000-0002-2749-7833</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5905388/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5905388/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,1411,4010,11541,27900,27901,27902,45550,45551,46027,46451,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29713471$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pickering, Raelene J</creatorcontrib><creatorcontrib>Rosado, Carlos J</creatorcontrib><creatorcontrib>Sharma, Arpeeta</creatorcontrib><creatorcontrib>Buksh, Shareefa</creatorcontrib><creatorcontrib>Tate, Mitchel</creatorcontrib><creatorcontrib>Haan, Judy B</creatorcontrib><title>Recent novel approaches to limit oxidative stress and inflammation in diabetic complications</title><title>Clinical & translational immunology</title><addtitle>Clin Transl Immunology</addtitle><description>Diabetes is considered a major burden on the healthcare system of Western and non‐Western societies with the disease reaching epidemic proportions globally. Diabetic patients are highly susceptible to developing micro‐ and macrovascular complications, which contribute significantly to morbidity and mortality rates. Over the past decade, a plethora of research has demonstrated that oxidative stress and inflammation are intricately linked and significant drivers of these diabetic complications. Thus, the focus now has been towards specific mechanism‐based strategies that can target both oxidative stress and inflammatory pathways to improve the outcome of disease burden. This review will focus on the mechanisms that drive these diabetic complications and the feasibility of emerging new therapies to combat oxidative stress and inflammation in the diabetic milieu.
Hyperglycaemia‐induced oxidative stress drives pro‐inflammatory pathways to mediate end‐organ injury resulting in diabetic micro‐ and macrovascular complications. Targeting these downstream pathways is offering new avenues for therapeutic interventions to limit these debilitating complications.</description><subject>Antioxidants</subject><subject>Atherosclerosis</subject><subject>Blood pressure</subject><subject>Cardiomyopathy</subject><subject>cardiovascular disease</subject><subject>chronic kidney disease</subject><subject>Clinical trials</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetic retinopathy</subject><subject>Drugs</subject><subject>Enzymes</subject><subject>Expenditures</subject><subject>Hyperglycemia</subject><subject>Inflammation</subject><subject>Kinases</subject><subject>Metabolism</subject><subject>Mitochondria</subject><subject>Morbidity</subject><subject>Nitric oxide</subject><subject>Oxidation</subject><subject>Oxidative stress</subject><subject>retinopathy</subject><subject>Risk factors</subject><issn>2050-0068</issn><issn>2050-0068</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kd9rFDEQx4MottQ--A9IwBd9ODtJbnPJiyCHPwoFQeqbELKzszYlu1mTvdP-92Z7tVTBp8xkPnyY4cvYcwFvBIA8wznIWgn9iB1LaGAFoM3jB_UROy3lGgCEWkMj9FN2JO2mNhtxzL59IaRx5mPaU-R-mnLyeEWFz4nHMISZp1-h83PYEy9zplK4Hzsexj76Yaj_aawN74JvaQ7IMQ1TDHg7KM_Yk97HQqd37wn7-uH95fbT6uLzx_Ptu4sVNmD1itYCsTHWiJYQLBpJ2kC3Fkrahnq0vl0rlLIVVusOe-g0tq3xG2FIetDqhL09eKddO1C3HJR9dFMOg883Lvng_p6M4cp9T3vXWGiUMVXw6k6Q048dldkNoSDF6EdKu-IkKKWMlo2s6Mt_0Ou0y2M9z0mptbJGbhbh6wOFOZWSqb9fRoBbYnNLbG6JrbIvHm5_T_4JqQJnB-BniHTzf5PbXp7LW-Vvk2ui6g</recordid><startdate>2018</startdate><enddate>2018</enddate><creator>Pickering, Raelene J</creator><creator>Rosado, Carlos J</creator><creator>Sharma, Arpeeta</creator><creator>Buksh, Shareefa</creator><creator>Tate, Mitchel</creator><creator>Haan, Judy B</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2749-7833</orcidid></search><sort><creationdate>2018</creationdate><title>Recent novel approaches to limit oxidative stress and inflammation in diabetic complications</title><author>Pickering, Raelene J ; Rosado, Carlos J ; Sharma, Arpeeta ; Buksh, Shareefa ; Tate, Mitchel ; Haan, Judy B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5096-e41cc58981bec09c82e680d413295efc9ab43c22b1966dcf0d6cbb8a718e2a063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Antioxidants</topic><topic>Atherosclerosis</topic><topic>Blood pressure</topic><topic>Cardiomyopathy</topic><topic>cardiovascular disease</topic><topic>chronic kidney disease</topic><topic>Clinical trials</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetic retinopathy</topic><topic>Drugs</topic><topic>Enzymes</topic><topic>Expenditures</topic><topic>Hyperglycemia</topic><topic>Inflammation</topic><topic>Kinases</topic><topic>Metabolism</topic><topic>Mitochondria</topic><topic>Morbidity</topic><topic>Nitric oxide</topic><topic>Oxidation</topic><topic>Oxidative stress</topic><topic>retinopathy</topic><topic>Risk factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pickering, Raelene J</creatorcontrib><creatorcontrib>Rosado, Carlos J</creatorcontrib><creatorcontrib>Sharma, Arpeeta</creatorcontrib><creatorcontrib>Buksh, Shareefa</creatorcontrib><creatorcontrib>Tate, Mitchel</creatorcontrib><creatorcontrib>Haan, Judy B</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</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>PubMed Central (Full Participant titles)</collection><jtitle>Clinical & translational immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pickering, Raelene J</au><au>Rosado, Carlos J</au><au>Sharma, Arpeeta</au><au>Buksh, Shareefa</au><au>Tate, Mitchel</au><au>Haan, Judy B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Recent novel approaches to limit oxidative stress and inflammation in diabetic complications</atitle><jtitle>Clinical & translational immunology</jtitle><addtitle>Clin Transl Immunology</addtitle><date>2018</date><risdate>2018</risdate><volume>7</volume><issue>4</issue><spage>e1016</spage><epage>n/a</epage><pages>e1016-n/a</pages><issn>2050-0068</issn><eissn>2050-0068</eissn><abstract>Diabetes is considered a major burden on the healthcare system of Western and non‐Western societies with the disease reaching epidemic proportions globally. Diabetic patients are highly susceptible to developing micro‐ and macrovascular complications, which contribute significantly to morbidity and mortality rates. Over the past decade, a plethora of research has demonstrated that oxidative stress and inflammation are intricately linked and significant drivers of these diabetic complications. Thus, the focus now has been towards specific mechanism‐based strategies that can target both oxidative stress and inflammatory pathways to improve the outcome of disease burden. This review will focus on the mechanisms that drive these diabetic complications and the feasibility of emerging new therapies to combat oxidative stress and inflammation in the diabetic milieu.
Hyperglycaemia‐induced oxidative stress drives pro‐inflammatory pathways to mediate end‐organ injury resulting in diabetic micro‐ and macrovascular complications. Targeting these downstream pathways is offering new avenues for therapeutic interventions to limit these debilitating complications.</abstract><cop>Australia</cop><pub>John Wiley & Sons, Inc</pub><pmid>29713471</pmid><doi>10.1002/cti2.1016</doi><tpages>20</tpages><orcidid>https://orcid.org/0000-0002-2749-7833</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antioxidants Atherosclerosis Blood pressure Cardiomyopathy cardiovascular disease chronic kidney disease Clinical trials Diabetes Diabetes mellitus Diabetic retinopathy Drugs Enzymes Expenditures Hyperglycemia Inflammation Kinases Metabolism Mitochondria Morbidity Nitric oxide Oxidation Oxidative stress retinopathy Risk factors |
title | Recent novel approaches to limit oxidative stress and inflammation in diabetic complications |
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