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Subcutaneous injection of hydrogen gas is a novel effective treatment for type 2 diabetes
AIMS/INTRODUCTION: In previous studies, hydrogen gas (H(2)) administration has clearly shown effectiveness in inhibiting diabetes. Here, we evaluated whether subcutaneous injection of H(2) shows enhanced efficacy against type 2 diabetes mellitus induced in mice by a high‐fat diet and low‐dose strept...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754517/ https://www.ncbi.nlm.nih.gov/pubmed/28390099 http://dx.doi.org/10.1111/jdi.12674 |
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author | Zhang, Xiaolong Liu, Jiaming Jin, Keke Xu, Haifeng Wang, Chuang Zhang, Zhuang Kong, Mimi Zhang, Zhengzheng Wang, Qingyi Wang, Fangyan |
author_facet | Zhang, Xiaolong Liu, Jiaming Jin, Keke Xu, Haifeng Wang, Chuang Zhang, Zhuang Kong, Mimi Zhang, Zhengzheng Wang, Qingyi Wang, Fangyan |
author_sort | Zhang, Xiaolong |
collection | PubMed |
description | AIMS/INTRODUCTION: In previous studies, hydrogen gas (H(2)) administration has clearly shown effectiveness in inhibiting diabetes. Here, we evaluated whether subcutaneous injection of H(2) shows enhanced efficacy against type 2 diabetes mellitus induced in mice by a high‐fat diet and low‐dose streptozotocin treatment. MATERIAL AND METHODS: H(2) was injected subcutaneously at a dose of 1 mL/mouse/week for 4 weeks. Type 2 diabetes mellitus‐associated parameters were then evaluated to determine the effectiveness of subcutaneous H(2) administration. RESULTS: The bodyweight of H(2)‐treated mice did not change over the course of the experiment. Compared with the untreated control animals, glucose, insulin, low‐density lipoprotein and triglyceride levels in the serum were significantly lower in treated mice, whereas high‐density lipoprotein cholesterol in the serum was significantly higher. Glucose tolerance and insulin sensitivity were both improved in H(2)‐treated mice. Diabetic nephropathy analysis showed significant reductions in urine volume, urinary total protein and β2‐microglobulin, kidney/bodyweight ratio, and kidney fibrosis associated with subcutaneous injection of H(2). CONCLUSIONS: Subcutaneous injection of H(2) significantly improves type 2 diabetes mellitus and diabetic nephropathy‐related outcomes in a mouse model, supporting further consideration of subcutaneous injection as a novel and effective route of clinical H(2) administration. |
format | Online Article Text |
id | pubmed-5754517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57545172018-01-09 Subcutaneous injection of hydrogen gas is a novel effective treatment for type 2 diabetes Zhang, Xiaolong Liu, Jiaming Jin, Keke Xu, Haifeng Wang, Chuang Zhang, Zhuang Kong, Mimi Zhang, Zhengzheng Wang, Qingyi Wang, Fangyan J Diabetes Investig Articles AIMS/INTRODUCTION: In previous studies, hydrogen gas (H(2)) administration has clearly shown effectiveness in inhibiting diabetes. Here, we evaluated whether subcutaneous injection of H(2) shows enhanced efficacy against type 2 diabetes mellitus induced in mice by a high‐fat diet and low‐dose streptozotocin treatment. MATERIAL AND METHODS: H(2) was injected subcutaneously at a dose of 1 mL/mouse/week for 4 weeks. Type 2 diabetes mellitus‐associated parameters were then evaluated to determine the effectiveness of subcutaneous H(2) administration. RESULTS: The bodyweight of H(2)‐treated mice did not change over the course of the experiment. Compared with the untreated control animals, glucose, insulin, low‐density lipoprotein and triglyceride levels in the serum were significantly lower in treated mice, whereas high‐density lipoprotein cholesterol in the serum was significantly higher. Glucose tolerance and insulin sensitivity were both improved in H(2)‐treated mice. Diabetic nephropathy analysis showed significant reductions in urine volume, urinary total protein and β2‐microglobulin, kidney/bodyweight ratio, and kidney fibrosis associated with subcutaneous injection of H(2). CONCLUSIONS: Subcutaneous injection of H(2) significantly improves type 2 diabetes mellitus and diabetic nephropathy‐related outcomes in a mouse model, supporting further consideration of subcutaneous injection as a novel and effective route of clinical H(2) administration. John Wiley and Sons Inc. 2017-05-18 2018-01 /pmc/articles/PMC5754517/ /pubmed/28390099 http://dx.doi.org/10.1111/jdi.12674 Text en © 2017 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Articles Zhang, Xiaolong Liu, Jiaming Jin, Keke Xu, Haifeng Wang, Chuang Zhang, Zhuang Kong, Mimi Zhang, Zhengzheng Wang, Qingyi Wang, Fangyan Subcutaneous injection of hydrogen gas is a novel effective treatment for type 2 diabetes |
title | Subcutaneous injection of hydrogen gas is a novel effective treatment for type 2 diabetes |
title_full | Subcutaneous injection of hydrogen gas is a novel effective treatment for type 2 diabetes |
title_fullStr | Subcutaneous injection of hydrogen gas is a novel effective treatment for type 2 diabetes |
title_full_unstemmed | Subcutaneous injection of hydrogen gas is a novel effective treatment for type 2 diabetes |
title_short | Subcutaneous injection of hydrogen gas is a novel effective treatment for type 2 diabetes |
title_sort | subcutaneous injection of hydrogen gas is a novel effective treatment for type 2 diabetes |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754517/ https://www.ncbi.nlm.nih.gov/pubmed/28390099 http://dx.doi.org/10.1111/jdi.12674 |
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