Improvement of cardiac dysfunction by bilateral surgical renal denervation in animals with diabetes induced by high fructose and high fat diet
Abstract Aims Insulin resistance (IR) and sympathetic over-activation play a critical role in diabetic cardiomyopathy (DCM). Percutaneous renal sympathetic denervation (RDN) was tested to treat refractory hypertension. However, the benefits of RDN for DCM and IR still remain unknown. The present stu...
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Veröffentlicht in: | Diabetes research and clinical practice 2016-05, Vol.115, p.140-149 |
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description | Abstract Aims Insulin resistance (IR) and sympathetic over-activation play a critical role in diabetic cardiomyopathy (DCM). Percutaneous renal sympathetic denervation (RDN) was tested to treat refractory hypertension. However, the benefits of RDN for DCM and IR still remain unknown. The present study aimed to investigate the effect and associated mechanisms of bilateral surgical RDN (bsRDN) on cardiac function and glucose metabolism in animals with diabetes. Methods Thirty-two male New Zealand white rabbits were randomly assigned to Chow ( n = 8, normal diet) and TEST ( n = 24, high-fructose fat diet [HFD]) groups. At 48 weeks after HFD feeding, animals in the TEST group were randomized to the Sham, HFD, and RDN subgroups and were fed a HFD for an additional 8 weeks. Repeated measurements of cardiac function, IR, apoptosis/autophagy, and histopathological assessment were performed at 48 and 56 weeks. Results HFD feeding for 56 weeks induced IR and diastolic cardiac dysfunction with hypertrophy in septum but well preserved eject fraction in the animals. Impaired IR further deteriorated over the time in the RDN group, featured by a more profound reduction in GLUT4 mRNA and its translocation to the plasma membrane. Successful denervation was associated with improvement of cardiac function via preventing myocardial fibrosis and over-expression of procollagen III, mammalian target of rapamycin, and cardiac apoptosis. Cardiac autophagy, assessed by either electron microscopy or Western blot, was enhanced by bsRDN. Conclusions Renal sympathetic denervation led to a significant improvement of HFD-induced cardiac dysfunction by shifting the cardiac apoptosis to autophagy, but worsening IR. Further study is required to identify the clinical benefits of RDN. |
doi_str_mv | 10.1016/j.diabres.2015.12.012 |
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Percutaneous renal sympathetic denervation (RDN) was tested to treat refractory hypertension. However, the benefits of RDN for DCM and IR still remain unknown. The present study aimed to investigate the effect and associated mechanisms of bilateral surgical RDN (bsRDN) on cardiac function and glucose metabolism in animals with diabetes. Methods Thirty-two male New Zealand white rabbits were randomly assigned to Chow ( n = 8, normal diet) and TEST ( n = 24, high-fructose fat diet [HFD]) groups. At 48 weeks after HFD feeding, animals in the TEST group were randomized to the Sham, HFD, and RDN subgroups and were fed a HFD for an additional 8 weeks. Repeated measurements of cardiac function, IR, apoptosis/autophagy, and histopathological assessment were performed at 48 and 56 weeks. Results HFD feeding for 56 weeks induced IR and diastolic cardiac dysfunction with hypertrophy in septum but well preserved eject fraction in the animals. Impaired IR further deteriorated over the time in the RDN group, featured by a more profound reduction in GLUT4 mRNA and its translocation to the plasma membrane. Successful denervation was associated with improvement of cardiac function via preventing myocardial fibrosis and over-expression of procollagen III, mammalian target of rapamycin, and cardiac apoptosis. Cardiac autophagy, assessed by either electron microscopy or Western blot, was enhanced by bsRDN. Conclusions Renal sympathetic denervation led to a significant improvement of HFD-induced cardiac dysfunction by shifting the cardiac apoptosis to autophagy, but worsening IR. Further study is required to identify the clinical benefits of RDN.</description><identifier>ISSN: 0168-8227</identifier><identifier>EISSN: 1872-8227</identifier><identifier>DOI: 10.1016/j.diabres.2015.12.012</identifier><identifier>PMID: 26997210</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Animals ; Apoptosis ; Autophagy ; Bilateral surgical renal denervation ; Denervation - methods ; Diabetes Mellitus, Experimental - complications ; Diabetic Cardiomyopathies - complications ; Diabetic Cardiomyopathies - diagnosis ; Diabetic Cardiomyopathies - therapy ; Diabetic cardiomyopathy ; Diet, High-Fat - adverse effects ; Echocardiography ; Endocrinology & Metabolism ; Fructose - toxicity ; Heart Ventricles - ultrastructure ; Insulin resistance ; Kidney - innervation ; Male ; Microscopy, Electron ; Myocardium - ultrastructure ; Rabbits ; Ventricular Dysfunction, Left - diagnosis ; Ventricular Dysfunction, Left - etiology ; Ventricular Dysfunction, Left - therapy</subject><ispartof>Diabetes research and clinical practice, 2016-05, Vol.115, p.140-149</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2016 Elsevier Ireland Ltd</rights><rights>Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-9bb4665044b1d4a816e687df728115e6c6148f3cdcb1380f4c0ac0d53a9e8233</citedby><cites>FETCH-LOGICAL-c420t-9bb4665044b1d4a816e687df728115e6c6148f3cdcb1380f4c0ac0d53a9e8233</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.diabres.2015.12.012$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26997210$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, YanRong</creatorcontrib><creatorcontrib>Li, Bing</creatorcontrib><creatorcontrib>Li, MingHui</creatorcontrib><creatorcontrib>Yu, YiHui</creatorcontrib><creatorcontrib>Wang, ZhiMei</creatorcontrib><creatorcontrib>Chen, ShaoLiang</creatorcontrib><title>Improvement of cardiac dysfunction by bilateral surgical renal denervation in animals with diabetes induced by high fructose and high fat diet</title><title>Diabetes research and clinical practice</title><addtitle>Diabetes Res Clin Pract</addtitle><description>Abstract Aims Insulin resistance (IR) and sympathetic over-activation play a critical role in diabetic cardiomyopathy (DCM). Percutaneous renal sympathetic denervation (RDN) was tested to treat refractory hypertension. However, the benefits of RDN for DCM and IR still remain unknown. The present study aimed to investigate the effect and associated mechanisms of bilateral surgical RDN (bsRDN) on cardiac function and glucose metabolism in animals with diabetes. Methods Thirty-two male New Zealand white rabbits were randomly assigned to Chow ( n = 8, normal diet) and TEST ( n = 24, high-fructose fat diet [HFD]) groups. At 48 weeks after HFD feeding, animals in the TEST group were randomized to the Sham, HFD, and RDN subgroups and were fed a HFD for an additional 8 weeks. Repeated measurements of cardiac function, IR, apoptosis/autophagy, and histopathological assessment were performed at 48 and 56 weeks. Results HFD feeding for 56 weeks induced IR and diastolic cardiac dysfunction with hypertrophy in septum but well preserved eject fraction in the animals. Impaired IR further deteriorated over the time in the RDN group, featured by a more profound reduction in GLUT4 mRNA and its translocation to the plasma membrane. Successful denervation was associated with improvement of cardiac function via preventing myocardial fibrosis and over-expression of procollagen III, mammalian target of rapamycin, and cardiac apoptosis. Cardiac autophagy, assessed by either electron microscopy or Western blot, was enhanced by bsRDN. Conclusions Renal sympathetic denervation led to a significant improvement of HFD-induced cardiac dysfunction by shifting the cardiac apoptosis to autophagy, but worsening IR. Further study is required to identify the clinical benefits of RDN.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Autophagy</subject><subject>Bilateral surgical renal denervation</subject><subject>Denervation - methods</subject><subject>Diabetes Mellitus, Experimental - complications</subject><subject>Diabetic Cardiomyopathies - complications</subject><subject>Diabetic Cardiomyopathies - diagnosis</subject><subject>Diabetic Cardiomyopathies - therapy</subject><subject>Diabetic cardiomyopathy</subject><subject>Diet, High-Fat - adverse effects</subject><subject>Echocardiography</subject><subject>Endocrinology & Metabolism</subject><subject>Fructose - toxicity</subject><subject>Heart Ventricles - ultrastructure</subject><subject>Insulin resistance</subject><subject>Kidney - innervation</subject><subject>Male</subject><subject>Microscopy, Electron</subject><subject>Myocardium - ultrastructure</subject><subject>Rabbits</subject><subject>Ventricular Dysfunction, Left - diagnosis</subject><subject>Ventricular Dysfunction, Left - etiology</subject><subject>Ventricular Dysfunction, Left - therapy</subject><issn>0168-8227</issn><issn>1872-8227</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUk1v1DAQjRCILoWfAPKRywaPkzjOBYQqPipV4kDvlmNPul4Sp9jOVvsn-M1MugsHLlxsy37vjd-8KYrXwEvgIN_tS-dNHzGVgkNTgig5iCfFBlQrtkqI9mmxIZx6PF8UL1Lac85lVTfPiwshu64VwDfFr-vpPs4HnDBkNg_Mmki6lrljGpZgs58D64-s96PJGM3I0hLvvKVDxECrw4DxYB5xPjAT_GTGxB583rH1g5gx0YNbLLpVaOfvdmyIi81zQoK7843JBMf8sng2EB9fnffL4vbzp9urr9ubb1-urz7ebG0teN52fV9L2fC67sHVRoFEqVo3tEIBNCithFoNlXW2h0rxobbcWO6aynSoRFVdFm9PsuT954Ip68kni-NoAs5L0tB2lQDRio6gzQlq45xSxEHfR_IYjxq4XpPQe31OQq9JaBCakiDem3OJpZ_Q_WX9aT0BPpwASD4PHqNO1mOgPvmINms3-_-WeP-Pgh19WMP5gUdM-3mJFBG50YkI-vs6Dus0gKRJAKWq3zd1s8E</recordid><startdate>20160501</startdate><enddate>20160501</enddate><creator>Liu, YanRong</creator><creator>Li, Bing</creator><creator>Li, MingHui</creator><creator>Yu, YiHui</creator><creator>Wang, ZhiMei</creator><creator>Chen, ShaoLiang</creator><general>Elsevier Ireland Ltd</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>7X8</scope></search><sort><creationdate>20160501</creationdate><title>Improvement of cardiac dysfunction by bilateral surgical renal denervation in animals with diabetes induced by high fructose and high fat diet</title><author>Liu, YanRong ; Li, Bing ; Li, MingHui ; Yu, YiHui ; Wang, ZhiMei ; Chen, ShaoLiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-9bb4665044b1d4a816e687df728115e6c6148f3cdcb1380f4c0ac0d53a9e8233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Autophagy</topic><topic>Bilateral surgical renal denervation</topic><topic>Denervation - methods</topic><topic>Diabetes Mellitus, Experimental - complications</topic><topic>Diabetic Cardiomyopathies - complications</topic><topic>Diabetic Cardiomyopathies - diagnosis</topic><topic>Diabetic Cardiomyopathies - therapy</topic><topic>Diabetic cardiomyopathy</topic><topic>Diet, High-Fat - adverse effects</topic><topic>Echocardiography</topic><topic>Endocrinology & Metabolism</topic><topic>Fructose - toxicity</topic><topic>Heart Ventricles - ultrastructure</topic><topic>Insulin resistance</topic><topic>Kidney - innervation</topic><topic>Male</topic><topic>Microscopy, Electron</topic><topic>Myocardium - ultrastructure</topic><topic>Rabbits</topic><topic>Ventricular Dysfunction, Left - diagnosis</topic><topic>Ventricular Dysfunction, Left - etiology</topic><topic>Ventricular Dysfunction, Left - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, YanRong</creatorcontrib><creatorcontrib>Li, Bing</creatorcontrib><creatorcontrib>Li, MingHui</creatorcontrib><creatorcontrib>Yu, YiHui</creatorcontrib><creatorcontrib>Wang, ZhiMei</creatorcontrib><creatorcontrib>Chen, ShaoLiang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Diabetes research and clinical practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, YanRong</au><au>Li, Bing</au><au>Li, MingHui</au><au>Yu, YiHui</au><au>Wang, ZhiMei</au><au>Chen, ShaoLiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Improvement of cardiac dysfunction by bilateral surgical renal denervation in animals with diabetes induced by high fructose and high fat diet</atitle><jtitle>Diabetes research and clinical practice</jtitle><addtitle>Diabetes Res Clin Pract</addtitle><date>2016-05-01</date><risdate>2016</risdate><volume>115</volume><spage>140</spage><epage>149</epage><pages>140-149</pages><issn>0168-8227</issn><eissn>1872-8227</eissn><abstract>Abstract Aims Insulin resistance (IR) and sympathetic over-activation play a critical role in diabetic cardiomyopathy (DCM). Percutaneous renal sympathetic denervation (RDN) was tested to treat refractory hypertension. However, the benefits of RDN for DCM and IR still remain unknown. The present study aimed to investigate the effect and associated mechanisms of bilateral surgical RDN (bsRDN) on cardiac function and glucose metabolism in animals with diabetes. Methods Thirty-two male New Zealand white rabbits were randomly assigned to Chow ( n = 8, normal diet) and TEST ( n = 24, high-fructose fat diet [HFD]) groups. At 48 weeks after HFD feeding, animals in the TEST group were randomized to the Sham, HFD, and RDN subgroups and were fed a HFD for an additional 8 weeks. Repeated measurements of cardiac function, IR, apoptosis/autophagy, and histopathological assessment were performed at 48 and 56 weeks. Results HFD feeding for 56 weeks induced IR and diastolic cardiac dysfunction with hypertrophy in septum but well preserved eject fraction in the animals. Impaired IR further deteriorated over the time in the RDN group, featured by a more profound reduction in GLUT4 mRNA and its translocation to the plasma membrane. Successful denervation was associated with improvement of cardiac function via preventing myocardial fibrosis and over-expression of procollagen III, mammalian target of rapamycin, and cardiac apoptosis. Cardiac autophagy, assessed by either electron microscopy or Western blot, was enhanced by bsRDN. Conclusions Renal sympathetic denervation led to a significant improvement of HFD-induced cardiac dysfunction by shifting the cardiac apoptosis to autophagy, but worsening IR. Further study is required to identify the clinical benefits of RDN.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>26997210</pmid><doi>10.1016/j.diabres.2015.12.012</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Apoptosis Autophagy Bilateral surgical renal denervation Denervation - methods Diabetes Mellitus, Experimental - complications Diabetic Cardiomyopathies - complications Diabetic Cardiomyopathies - diagnosis Diabetic Cardiomyopathies - therapy Diabetic cardiomyopathy Diet, High-Fat - adverse effects Echocardiography Endocrinology & Metabolism Fructose - toxicity Heart Ventricles - ultrastructure Insulin resistance Kidney - innervation Male Microscopy, Electron Myocardium - ultrastructure Rabbits Ventricular Dysfunction, Left - diagnosis Ventricular Dysfunction, Left - etiology Ventricular Dysfunction, Left - therapy |
title | Improvement of cardiac dysfunction by bilateral surgical renal denervation in animals with diabetes induced by high fructose and high fat diet |
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