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Influence of oxidative stress on vascular calcification in the setting of coexisting chronic kidney disease and diabetes mellitus

Vascular calcification (VC) is a common complication in patients with chronic kidney disease (CKD). Particularly, CKD patients with diabetes mellitus (DM) develop severe VC. Specific mechanisms of VC remain unclear; this study aimed to investigate them in the context of coexisting CKD and DM, mainly...

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Autores principales: Watanabe, Shuhei, Fujii, Hideki, Kono, Keiji, Watanabe, Kentaro, Goto, Shunsuke, Nishi, Shinichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693179/
https://www.ncbi.nlm.nih.gov/pubmed/33244056
http://dx.doi.org/10.1038/s41598-020-76838-0
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author Watanabe, Shuhei
Fujii, Hideki
Kono, Keiji
Watanabe, Kentaro
Goto, Shunsuke
Nishi, Shinichi
author_facet Watanabe, Shuhei
Fujii, Hideki
Kono, Keiji
Watanabe, Kentaro
Goto, Shunsuke
Nishi, Shinichi
author_sort Watanabe, Shuhei
collection PubMed
description Vascular calcification (VC) is a common complication in patients with chronic kidney disease (CKD). Particularly, CKD patients with diabetes mellitus (DM) develop severe VC. Specific mechanisms of VC remain unclear; this study aimed to investigate them in the context of coexisting CKD and DM, mainly regarding oxidative stress. Sprague Dawley rats were randomly divided into six groups as follows: control rats (Control), 5/6 nephrectomized rats (CKD), streptozotocin-injected rats (DM), 5/6 nephrectomized and streptozotocin-injected rats (CKD + DM), CKD + DM rats treated with insulin (CKD + DM + INS), and CKD + DM rats treated with antioxidant apocynin (CKD + DM + APO). At 18 weeks old, the rats were sacrificed for analysis. Compared to the control, DM and CKD groups, calcification of aortas significantly increased in the CKD + DM group. Oxidative stress and osteoblast differentiation-related markers considerably increased in the CKD + DM group compared with the other groups. Moreover, apocynin considerably reduced oxidative stress, osteoblast differentiation-related markers, and aortic calcification despite high blood glucose levels. Our data indicate that coexisting CKD and DM hasten VC primarily through an increase in oxidative stress; anti-oxidative therapy may prevent the VC progression.
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spelling pubmed-76931792020-11-30 Influence of oxidative stress on vascular calcification in the setting of coexisting chronic kidney disease and diabetes mellitus Watanabe, Shuhei Fujii, Hideki Kono, Keiji Watanabe, Kentaro Goto, Shunsuke Nishi, Shinichi Sci Rep Article Vascular calcification (VC) is a common complication in patients with chronic kidney disease (CKD). Particularly, CKD patients with diabetes mellitus (DM) develop severe VC. Specific mechanisms of VC remain unclear; this study aimed to investigate them in the context of coexisting CKD and DM, mainly regarding oxidative stress. Sprague Dawley rats were randomly divided into six groups as follows: control rats (Control), 5/6 nephrectomized rats (CKD), streptozotocin-injected rats (DM), 5/6 nephrectomized and streptozotocin-injected rats (CKD + DM), CKD + DM rats treated with insulin (CKD + DM + INS), and CKD + DM rats treated with antioxidant apocynin (CKD + DM + APO). At 18 weeks old, the rats were sacrificed for analysis. Compared to the control, DM and CKD groups, calcification of aortas significantly increased in the CKD + DM group. Oxidative stress and osteoblast differentiation-related markers considerably increased in the CKD + DM group compared with the other groups. Moreover, apocynin considerably reduced oxidative stress, osteoblast differentiation-related markers, and aortic calcification despite high blood glucose levels. Our data indicate that coexisting CKD and DM hasten VC primarily through an increase in oxidative stress; anti-oxidative therapy may prevent the VC progression. Nature Publishing Group UK 2020-11-26 /pmc/articles/PMC7693179/ /pubmed/33244056 http://dx.doi.org/10.1038/s41598-020-76838-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Watanabe, Shuhei
Fujii, Hideki
Kono, Keiji
Watanabe, Kentaro
Goto, Shunsuke
Nishi, Shinichi
Influence of oxidative stress on vascular calcification in the setting of coexisting chronic kidney disease and diabetes mellitus
title Influence of oxidative stress on vascular calcification in the setting of coexisting chronic kidney disease and diabetes mellitus
title_full Influence of oxidative stress on vascular calcification in the setting of coexisting chronic kidney disease and diabetes mellitus
title_fullStr Influence of oxidative stress on vascular calcification in the setting of coexisting chronic kidney disease and diabetes mellitus
title_full_unstemmed Influence of oxidative stress on vascular calcification in the setting of coexisting chronic kidney disease and diabetes mellitus
title_short Influence of oxidative stress on vascular calcification in the setting of coexisting chronic kidney disease and diabetes mellitus
title_sort influence of oxidative stress on vascular calcification in the setting of coexisting chronic kidney disease and diabetes mellitus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693179/
https://www.ncbi.nlm.nih.gov/pubmed/33244056
http://dx.doi.org/10.1038/s41598-020-76838-0
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