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Optimal LDR to Protect the Kidney From Diabetes: Whole-Body Exposure to 25 mGy X-rays Weekly for 8 Weeks Efficiently Attenuates Renal Damage in Diabetic Mice

To explore an optimal frequency of whole-body low-dose radiation (LDR) to protect the kidney from diabetes, type 1 diabetic mice were induced with multiple injections of low-dose streptozotocin in male C57BL/6J mice. Diabetic or age-matched normal mice received whole-body exposure to 12.5 or 25 mGy...

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Autores principales: Cheng, Jie, Li, Fengsheng, Wang, Guanjun, Guo, Weiying, Huang, Shan, Wang, Brain, Li, Cai, Jiang, Qisheng, Cai, Lu, Cui, Jiuwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130090/
https://www.ncbi.nlm.nih.gov/pubmed/30210268
http://dx.doi.org/10.1177/1559325818789843
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author Cheng, Jie
Li, Fengsheng
Wang, Guanjun
Guo, Weiying
Huang, Shan
Wang, Brain
Li, Cai
Jiang, Qisheng
Cai, Lu
Cui, Jiuwei
author_facet Cheng, Jie
Li, Fengsheng
Wang, Guanjun
Guo, Weiying
Huang, Shan
Wang, Brain
Li, Cai
Jiang, Qisheng
Cai, Lu
Cui, Jiuwei
author_sort Cheng, Jie
collection PubMed
description To explore an optimal frequency of whole-body low-dose radiation (LDR) to protect the kidney from diabetes, type 1 diabetic mice were induced with multiple injections of low-dose streptozotocin in male C57BL/6J mice. Diabetic or age-matched normal mice received whole-body exposure to 12.5 or 25 mGy either every other day or weekly for 4 or 8 weeks. Diabetes decreased the urinary creatinine and increased the microalbumin in urine, renal accumulation of 3-nitrotyrosine and 4-hydroxynonenal, and renal expression of collagen IV and fibronectin. All these renal pathological and functional changes in diabetic mice were significantly attenuated by exposure to LDR at all regimens. However, whole-body exposure of diabetic mice to 25 mGy weekly and to 12.5 mGy every other day for 8 weeks provided a better prevention of diabetic nephropathy than other LDR regimens. Furthermore, whole-body exposure to 25 mGy weekly for 8 weeks showed no detectable effect on the kidney of normal mice, but whole-body exposure to normal mice at 12.5 mGy every other day for 8 weeks increased urinary microalbumin and renal expression of collagen IV and fibronectin. These results suggest that whole-body exposure to LDR at 25 mGy weekly is the optimal condition of LDR to protect the kidney from diabetes.
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spelling pubmed-61300902018-09-12 Optimal LDR to Protect the Kidney From Diabetes: Whole-Body Exposure to 25 mGy X-rays Weekly for 8 Weeks Efficiently Attenuates Renal Damage in Diabetic Mice Cheng, Jie Li, Fengsheng Wang, Guanjun Guo, Weiying Huang, Shan Wang, Brain Li, Cai Jiang, Qisheng Cai, Lu Cui, Jiuwei Dose Response Potential Clinical Implication of LDR Hormesis and Adaptive Response To explore an optimal frequency of whole-body low-dose radiation (LDR) to protect the kidney from diabetes, type 1 diabetic mice were induced with multiple injections of low-dose streptozotocin in male C57BL/6J mice. Diabetic or age-matched normal mice received whole-body exposure to 12.5 or 25 mGy either every other day or weekly for 4 or 8 weeks. Diabetes decreased the urinary creatinine and increased the microalbumin in urine, renal accumulation of 3-nitrotyrosine and 4-hydroxynonenal, and renal expression of collagen IV and fibronectin. All these renal pathological and functional changes in diabetic mice were significantly attenuated by exposure to LDR at all regimens. However, whole-body exposure of diabetic mice to 25 mGy weekly and to 12.5 mGy every other day for 8 weeks provided a better prevention of diabetic nephropathy than other LDR regimens. Furthermore, whole-body exposure to 25 mGy weekly for 8 weeks showed no detectable effect on the kidney of normal mice, but whole-body exposure to normal mice at 12.5 mGy every other day for 8 weeks increased urinary microalbumin and renal expression of collagen IV and fibronectin. These results suggest that whole-body exposure to LDR at 25 mGy weekly is the optimal condition of LDR to protect the kidney from diabetes. SAGE Publications 2018-09-06 /pmc/articles/PMC6130090/ /pubmed/30210268 http://dx.doi.org/10.1177/1559325818789843 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Potential Clinical Implication of LDR Hormesis and Adaptive Response
Cheng, Jie
Li, Fengsheng
Wang, Guanjun
Guo, Weiying
Huang, Shan
Wang, Brain
Li, Cai
Jiang, Qisheng
Cai, Lu
Cui, Jiuwei
Optimal LDR to Protect the Kidney From Diabetes: Whole-Body Exposure to 25 mGy X-rays Weekly for 8 Weeks Efficiently Attenuates Renal Damage in Diabetic Mice
title Optimal LDR to Protect the Kidney From Diabetes: Whole-Body Exposure to 25 mGy X-rays Weekly for 8 Weeks Efficiently Attenuates Renal Damage in Diabetic Mice
title_full Optimal LDR to Protect the Kidney From Diabetes: Whole-Body Exposure to 25 mGy X-rays Weekly for 8 Weeks Efficiently Attenuates Renal Damage in Diabetic Mice
title_fullStr Optimal LDR to Protect the Kidney From Diabetes: Whole-Body Exposure to 25 mGy X-rays Weekly for 8 Weeks Efficiently Attenuates Renal Damage in Diabetic Mice
title_full_unstemmed Optimal LDR to Protect the Kidney From Diabetes: Whole-Body Exposure to 25 mGy X-rays Weekly for 8 Weeks Efficiently Attenuates Renal Damage in Diabetic Mice
title_short Optimal LDR to Protect the Kidney From Diabetes: Whole-Body Exposure to 25 mGy X-rays Weekly for 8 Weeks Efficiently Attenuates Renal Damage in Diabetic Mice
title_sort optimal ldr to protect the kidney from diabetes: whole-body exposure to 25 mgy x-rays weekly for 8 weeks efficiently attenuates renal damage in diabetic mice
topic Potential Clinical Implication of LDR Hormesis and Adaptive Response
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130090/
https://www.ncbi.nlm.nih.gov/pubmed/30210268
http://dx.doi.org/10.1177/1559325818789843
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