The roles of sodium-glucose cotransporter 2 inhibitors in preventing kidney injury in diabetes

© 2017 Elsevier Masson SAS Diabetic nephropathy (DN) is the leading cause of end stage renal disease (ESRD) worldwide. The early effective treatment of high plasma glucose could delay or prevent the onset of DN. Sodium-glucose cotransporter 2 (SGLT2) inhibitors are new target treatments for ameliora...

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Main Authors: Krit Jaikumkao, Anchalee Pongchaidecha, Varanuj Chatsudthipong, Siriporn C. Chattipakorn, Nipon Chattipakorn, Anusorn Lungkaphin
Format: Journal
Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/47049
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spelling th-cmuir.6653943832-470492018-04-25T07:37:42Z The roles of sodium-glucose cotransporter 2 inhibitors in preventing kidney injury in diabetes Krit Jaikumkao Anchalee Pongchaidecha Varanuj Chatsudthipong Siriporn C. Chattipakorn Nipon Chattipakorn Anusorn Lungkaphin Agricultural and Biological Sciences Arts and Humanities © 2017 Elsevier Masson SAS Diabetic nephropathy (DN) is the leading cause of end stage renal disease (ESRD) worldwide. The early effective treatment of high plasma glucose could delay or prevent the onset of DN. Sodium-glucose cotransporter 2 (SGLT2) inhibitors are new target treatments for ameliorating high plasma glucose and help to maintain glucose homeostasis in diabetic patients. Reduced renal glucose reabsorption by SGLT2 inhibition seems to have high potential to improve glycemic control in diabetes mellitus (DM) not only through glucose lowering but also through glucose-independent effects such as blood pressure-lowering and direct renal effects in diabetes. Of note, the important events in the pathogenesis of glucose-induced renal injury and DN including oxidative stress, inflammation, fibrosis and apoptosis conditions have shown to be ameliorate after the treatment with SGLT2 inhibitors. Interestingly, SGLT2 inhibitors have been reported to reduce albuminuria in DM via an activation of renal tubuloglomerular feedback by increased macula densa sodium and chloride delivery, leading to afferent vasoconstriction and attenuated diabetes-induced renal hyperfiltration. These effects also help to conserve glomerular integrity. Thus, the treatment of diabetes mellitus using SGLT2 inhibitors could be one of the effective approach for the management of diabetic-associated kidney disease like DN. This review summarizes the up to date information and discusses the bidirectional relationship between the SGLT2 inhibitor treatments and the renal functions that are available from both basic research and clinical reports. The details of renal outcomes of SGLT2 inhibitors in DN are also provide in this review. 2018-04-25T07:15:45Z 2018-04-25T07:15:45Z 2017-10-01 Journal 19506007 07533322 2-s2.0-85026376186 10.1016/j.biopha.2017.07.095 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85026376186&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/47049
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Agricultural and Biological Sciences
Arts and Humanities
spellingShingle Agricultural and Biological Sciences
Arts and Humanities
Krit Jaikumkao
Anchalee Pongchaidecha
Varanuj Chatsudthipong
Siriporn C. Chattipakorn
Nipon Chattipakorn
Anusorn Lungkaphin
The roles of sodium-glucose cotransporter 2 inhibitors in preventing kidney injury in diabetes
description © 2017 Elsevier Masson SAS Diabetic nephropathy (DN) is the leading cause of end stage renal disease (ESRD) worldwide. The early effective treatment of high plasma glucose could delay or prevent the onset of DN. Sodium-glucose cotransporter 2 (SGLT2) inhibitors are new target treatments for ameliorating high plasma glucose and help to maintain glucose homeostasis in diabetic patients. Reduced renal glucose reabsorption by SGLT2 inhibition seems to have high potential to improve glycemic control in diabetes mellitus (DM) not only through glucose lowering but also through glucose-independent effects such as blood pressure-lowering and direct renal effects in diabetes. Of note, the important events in the pathogenesis of glucose-induced renal injury and DN including oxidative stress, inflammation, fibrosis and apoptosis conditions have shown to be ameliorate after the treatment with SGLT2 inhibitors. Interestingly, SGLT2 inhibitors have been reported to reduce albuminuria in DM via an activation of renal tubuloglomerular feedback by increased macula densa sodium and chloride delivery, leading to afferent vasoconstriction and attenuated diabetes-induced renal hyperfiltration. These effects also help to conserve glomerular integrity. Thus, the treatment of diabetes mellitus using SGLT2 inhibitors could be one of the effective approach for the management of diabetic-associated kidney disease like DN. This review summarizes the up to date information and discusses the bidirectional relationship between the SGLT2 inhibitor treatments and the renal functions that are available from both basic research and clinical reports. The details of renal outcomes of SGLT2 inhibitors in DN are also provide in this review.
format Journal
author Krit Jaikumkao
Anchalee Pongchaidecha
Varanuj Chatsudthipong
Siriporn C. Chattipakorn
Nipon Chattipakorn
Anusorn Lungkaphin
author_facet Krit Jaikumkao
Anchalee Pongchaidecha
Varanuj Chatsudthipong
Siriporn C. Chattipakorn
Nipon Chattipakorn
Anusorn Lungkaphin
author_sort Krit Jaikumkao
title The roles of sodium-glucose cotransporter 2 inhibitors in preventing kidney injury in diabetes
title_short The roles of sodium-glucose cotransporter 2 inhibitors in preventing kidney injury in diabetes
title_full The roles of sodium-glucose cotransporter 2 inhibitors in preventing kidney injury in diabetes
title_fullStr The roles of sodium-glucose cotransporter 2 inhibitors in preventing kidney injury in diabetes
title_full_unstemmed The roles of sodium-glucose cotransporter 2 inhibitors in preventing kidney injury in diabetes
title_sort roles of sodium-glucose cotransporter 2 inhibitors in preventing kidney injury in diabetes
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85026376186&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/47049
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