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Protective Effect of Keluoxin against Diabetic Nephropathy in Type 2 Diabetic Mellitus Models
Diabetic nephropathy (DN) is a chronic kidney disease that develops in patients with diabetes mellitus (DM). Renal dysfunction and persistent proteinuria are the main clinical features of DN. Podocyte injury is an important cause of persistent proteinuria and diabetic kidney disease (DKD) progressio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8548109/ https://www.ncbi.nlm.nih.gov/pubmed/34712350 http://dx.doi.org/10.1155/2021/8455709 |
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author | Yang, Xiaomei Han, Xuke Wen, Qing Qiu, Xianliang Deng, Huan Chen, Qiu |
author_facet | Yang, Xiaomei Han, Xuke Wen, Qing Qiu, Xianliang Deng, Huan Chen, Qiu |
author_sort | Yang, Xiaomei |
collection | PubMed |
description | Diabetic nephropathy (DN) is a chronic kidney disease that develops in patients with diabetes mellitus (DM). Renal dysfunction and persistent proteinuria are the main clinical features of DN. Podocyte injury is an important cause of persistent proteinuria and diabetic kidney disease (DKD) progression. Traditional Chinese patent medicines can improve renal function by enhancing autophagy and promoting apoptosis. Keluoxin is a Chinese patent medicine that has the effect of invigorating qi and nourishing yin, activating blood, and eliminating blood stasis. Therefore, we hypothesized that Keluoxin may have a protective effect against diabetic nephropathy in rats with type 2 DM. Rats induced with diabetes through streptozocin (STZ) injection and a high-fat and high-sugar diet were treated with Keluoxin (0.63 g/kg/day) for 8 weeks, and renal function, biochemical indicators, and histopathological changes in renal tissues were observed. Immunofluorescence staining and western blot analysis were used to detect the expression of autophagy-related proteins. The results showed that Keluoxin reduced blood glucose and lipid levels, improved renal function, and alleviated renal histopathological changes in rats with DN. The therapeutic effect was similar to that of Irbesartan (15.6 mg/kg/day). It is inferred that the mechanism works through reducing the obstruction of downstream pathways of autophagy by improving the lysosomal degradation function and alleviating podocyte injury. This study demonstrates that Keluoxin could regulate autophagy in podocytes, alleviate kidney injury in rats with DN, and have a protective effect on renal function; its mechanism can thus be a potential therapy for DN. |
format | Online Article Text |
id | pubmed-8548109 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-85481092021-10-27 Protective Effect of Keluoxin against Diabetic Nephropathy in Type 2 Diabetic Mellitus Models Yang, Xiaomei Han, Xuke Wen, Qing Qiu, Xianliang Deng, Huan Chen, Qiu Evid Based Complement Alternat Med Research Article Diabetic nephropathy (DN) is a chronic kidney disease that develops in patients with diabetes mellitus (DM). Renal dysfunction and persistent proteinuria are the main clinical features of DN. Podocyte injury is an important cause of persistent proteinuria and diabetic kidney disease (DKD) progression. Traditional Chinese patent medicines can improve renal function by enhancing autophagy and promoting apoptosis. Keluoxin is a Chinese patent medicine that has the effect of invigorating qi and nourishing yin, activating blood, and eliminating blood stasis. Therefore, we hypothesized that Keluoxin may have a protective effect against diabetic nephropathy in rats with type 2 DM. Rats induced with diabetes through streptozocin (STZ) injection and a high-fat and high-sugar diet were treated with Keluoxin (0.63 g/kg/day) for 8 weeks, and renal function, biochemical indicators, and histopathological changes in renal tissues were observed. Immunofluorescence staining and western blot analysis were used to detect the expression of autophagy-related proteins. The results showed that Keluoxin reduced blood glucose and lipid levels, improved renal function, and alleviated renal histopathological changes in rats with DN. The therapeutic effect was similar to that of Irbesartan (15.6 mg/kg/day). It is inferred that the mechanism works through reducing the obstruction of downstream pathways of autophagy by improving the lysosomal degradation function and alleviating podocyte injury. This study demonstrates that Keluoxin could regulate autophagy in podocytes, alleviate kidney injury in rats with DN, and have a protective effect on renal function; its mechanism can thus be a potential therapy for DN. Hindawi 2021-10-19 /pmc/articles/PMC8548109/ /pubmed/34712350 http://dx.doi.org/10.1155/2021/8455709 Text en Copyright © 2021 Xiaomei Yang et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Yang, Xiaomei Han, Xuke Wen, Qing Qiu, Xianliang Deng, Huan Chen, Qiu Protective Effect of Keluoxin against Diabetic Nephropathy in Type 2 Diabetic Mellitus Models |
title | Protective Effect of Keluoxin against Diabetic Nephropathy in Type 2 Diabetic Mellitus Models |
title_full | Protective Effect of Keluoxin against Diabetic Nephropathy in Type 2 Diabetic Mellitus Models |
title_fullStr | Protective Effect of Keluoxin against Diabetic Nephropathy in Type 2 Diabetic Mellitus Models |
title_full_unstemmed | Protective Effect of Keluoxin against Diabetic Nephropathy in Type 2 Diabetic Mellitus Models |
title_short | Protective Effect of Keluoxin against Diabetic Nephropathy in Type 2 Diabetic Mellitus Models |
title_sort | protective effect of keluoxin against diabetic nephropathy in type 2 diabetic mellitus models |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8548109/ https://www.ncbi.nlm.nih.gov/pubmed/34712350 http://dx.doi.org/10.1155/2021/8455709 |
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