Subcutaneous injection of hydrogen gas is a novel effective treatment for type 2 diabetes
Aims/Introduction In previous studies, hydrogen gas (H2) administration has clearly shown effectiveness in inhibiting diabetes. Here, we evaluated whether subcutaneous injection of H2 shows enhanced efficacy against type 2 diabetes mellitus induced in mice by a high‐fat diet and low‐dose streptozoto...
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Veröffentlicht in: | Journal of diabetes investigation 2018-01, Vol.9 (1), p.83-90 |
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creator | Zhang, Xiaolong Liu, Jiaming Jin, Keke Xu, Haifeng Wang, Chuang Zhang, Zhuang Kong, Mimi Zhang, Zhengzheng Wang, Qingyi Wang, Fangyan |
description | Aims/Introduction
In previous studies, hydrogen gas (H2) administration has clearly shown effectiveness in inhibiting diabetes. Here, we evaluated whether subcutaneous injection of H2 shows enhanced efficacy against type 2 diabetes mellitus induced in mice by a high‐fat diet and low‐dose streptozotocin treatment.
Material and Methods
H2 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 H2 administration.
Results
The bodyweight of H2‐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 H2‐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 H2.
Conclusions
Subcutaneous injection of H2 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 H2 administration.
Subcutaneous injection of H2 significantly improves type 2 diabetes mellitus and DN related outcomes in a mouse model, supporting further consideration of subcutaneous injection as a novel and effective route of clinical H2 administration. |
doi_str_mv | 10.1111/jdi.12674 |
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In previous studies, hydrogen gas (H2) administration has clearly shown effectiveness in inhibiting diabetes. Here, we evaluated whether subcutaneous injection of H2 shows enhanced efficacy against type 2 diabetes mellitus induced in mice by a high‐fat diet and low‐dose streptozotocin treatment.
Material and Methods
H2 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 H2 administration.
Results
The bodyweight of H2‐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 H2‐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 H2.
Conclusions
Subcutaneous injection of H2 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 H2 administration.
Subcutaneous injection of H2 significantly improves type 2 diabetes mellitus and DN related outcomes in a mouse model, supporting further consideration of subcutaneous injection as a novel and effective route of clinical H2 administration.</description><identifier>ISSN: 2040-1116</identifier><identifier>EISSN: 2040-1124</identifier><identifier>DOI: 10.1111/jdi.12674</identifier><identifier>PMID: 28390099</identifier><language>eng</language><publisher>Japan: John Wiley & Sons, Inc</publisher><subject>Animals ; Cholesterol ; Diabetes ; Diabetes mellitus ; Diabetes Mellitus, Experimental - therapy ; Diabetes Mellitus, Type 2 - complications ; Diabetes Mellitus, Type 2 - metabolism ; Diabetes Mellitus, Type 2 - therapy ; Diabetic Nephropathies - pathology ; Diabetic Nephropathies - therapy ; Diabetic nephropathy ; Diet, High-Fat ; Fibrosis ; Glucose tolerance ; High fat diet ; Hydrogen ; Hydrogen - administration & dosage ; Injection ; Injections, Subcutaneous ; Insulin ; Kidneys ; Male ; Mice, Inbred C57BL ; Nephropathy ; Original ; Oxidative Stress ; Rodents ; Streptozocin ; Subcutaneous administration ; Urine</subject><ispartof>Journal of diabetes investigation, 2018-01, Vol.9 (1), p.83-90</ispartof><rights>2017 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd</rights><rights>2017 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd.</rights><rights>2018. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4954-b69453d226f5ab7a283f071f27d547f34af8b71b73341cfe8f705eaa900c84973</citedby><cites>FETCH-LOGICAL-c4954-b69453d226f5ab7a283f071f27d547f34af8b71b73341cfe8f705eaa900c84973</cites><orcidid>0000-0003-0555-8495</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754517/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754517/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,1412,11543,27905,27906,45555,45556,46033,46457,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28390099$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Xiaolong</creatorcontrib><creatorcontrib>Liu, Jiaming</creatorcontrib><creatorcontrib>Jin, Keke</creatorcontrib><creatorcontrib>Xu, Haifeng</creatorcontrib><creatorcontrib>Wang, Chuang</creatorcontrib><creatorcontrib>Zhang, Zhuang</creatorcontrib><creatorcontrib>Kong, Mimi</creatorcontrib><creatorcontrib>Zhang, Zhengzheng</creatorcontrib><creatorcontrib>Wang, Qingyi</creatorcontrib><creatorcontrib>Wang, Fangyan</creatorcontrib><title>Subcutaneous injection of hydrogen gas is a novel effective treatment for type 2 diabetes</title><title>Journal of diabetes investigation</title><addtitle>J Diabetes Investig</addtitle><description>Aims/Introduction
In previous studies, hydrogen gas (H2) administration has clearly shown effectiveness in inhibiting diabetes. Here, we evaluated whether subcutaneous injection of H2 shows enhanced efficacy against type 2 diabetes mellitus induced in mice by a high‐fat diet and low‐dose streptozotocin treatment.
Material and Methods
H2 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 H2 administration.
Results
The bodyweight of H2‐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 H2‐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 H2.
Conclusions
Subcutaneous injection of H2 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 H2 administration.
Subcutaneous injection of H2 significantly improves type 2 diabetes mellitus and DN related outcomes in a mouse model, supporting further consideration of subcutaneous injection as a novel and effective route of clinical H2 administration.</description><subject>Animals</subject><subject>Cholesterol</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetes Mellitus, Experimental - therapy</subject><subject>Diabetes Mellitus, Type 2 - complications</subject><subject>Diabetes Mellitus, Type 2 - metabolism</subject><subject>Diabetes Mellitus, Type 2 - therapy</subject><subject>Diabetic Nephropathies - pathology</subject><subject>Diabetic Nephropathies - therapy</subject><subject>Diabetic nephropathy</subject><subject>Diet, High-Fat</subject><subject>Fibrosis</subject><subject>Glucose tolerance</subject><subject>High fat diet</subject><subject>Hydrogen</subject><subject>Hydrogen - administration & dosage</subject><subject>Injection</subject><subject>Injections, Subcutaneous</subject><subject>Insulin</subject><subject>Kidneys</subject><subject>Male</subject><subject>Mice, Inbred C57BL</subject><subject>Nephropathy</subject><subject>Original</subject><subject>Oxidative Stress</subject><subject>Rodents</subject><subject>Streptozocin</subject><subject>Subcutaneous administration</subject><subject>Urine</subject><issn>2040-1116</issn><issn>2040-1124</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp1kU9LwzAYh4MoKrqDX0ACXvQwTdqkSS-CzP8IHtSDp5C2b2ZG18yknezbm9k5VPC9JPA-PPySH0IHlJzSOGeTyp7SJBNsA-0mhJEhpQnbXN9ptoMGIUxInFTKLBPbaCeRaU5Inu-i16euKLtWN-C6gG0zgbK1rsHO4LdF5d0YGjzWcROwxo2bQ43BmCU0B9x60O0UmhYb53G7mAFOcGV1AS2EfbRldB1gsDr30Mv11fPodvjweHM3ungYliznbFhkOeNplSSZ4boQOkYzRFCTiIozYVKmjSwELUSaMloakEYQDlrH_KVkuUj30HnvnXXFFKoyxvG6VjNvp9ovlNNW_d409k2N3VxxwRmnS8HxSuDdewehVVMbSqjr_lMUlZLnnAgpI3r0B524zjfxeYrmkmWpiNJInfRU6V0IHsw6DCVq2ZmKnamvziJ7-DP9mvxuKAJnPfBha1j8b1L3l3e98hNlv6Bq</recordid><startdate>201801</startdate><enddate>201801</enddate><creator>Zhang, Xiaolong</creator><creator>Liu, Jiaming</creator><creator>Jin, Keke</creator><creator>Xu, Haifeng</creator><creator>Wang, Chuang</creator><creator>Zhang, Zhuang</creator><creator>Kong, Mimi</creator><creator>Zhang, Zhengzheng</creator><creator>Wang, Qingyi</creator><creator>Wang, Fangyan</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0555-8495</orcidid></search><sort><creationdate>201801</creationdate><title>Subcutaneous injection of hydrogen gas is a novel effective treatment for type 2 diabetes</title><author>Zhang, Xiaolong ; Liu, Jiaming ; Jin, Keke ; Xu, Haifeng ; Wang, Chuang ; Zhang, Zhuang ; Kong, Mimi ; Zhang, Zhengzheng ; Wang, Qingyi ; Wang, Fangyan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4954-b69453d226f5ab7a283f071f27d547f34af8b71b73341cfe8f705eaa900c84973</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Cholesterol</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetes Mellitus, Experimental - therapy</topic><topic>Diabetes Mellitus, Type 2 - complications</topic><topic>Diabetes Mellitus, Type 2 - metabolism</topic><topic>Diabetes Mellitus, Type 2 - therapy</topic><topic>Diabetic Nephropathies - pathology</topic><topic>Diabetic Nephropathies - therapy</topic><topic>Diabetic nephropathy</topic><topic>Diet, High-Fat</topic><topic>Fibrosis</topic><topic>Glucose tolerance</topic><topic>High fat diet</topic><topic>Hydrogen</topic><topic>Hydrogen - administration & dosage</topic><topic>Injection</topic><topic>Injections, Subcutaneous</topic><topic>Insulin</topic><topic>Kidneys</topic><topic>Male</topic><topic>Mice, Inbred C57BL</topic><topic>Nephropathy</topic><topic>Original</topic><topic>Oxidative Stress</topic><topic>Rodents</topic><topic>Streptozocin</topic><topic>Subcutaneous administration</topic><topic>Urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Xiaolong</creatorcontrib><creatorcontrib>Liu, Jiaming</creatorcontrib><creatorcontrib>Jin, Keke</creatorcontrib><creatorcontrib>Xu, Haifeng</creatorcontrib><creatorcontrib>Wang, Chuang</creatorcontrib><creatorcontrib>Zhang, Zhuang</creatorcontrib><creatorcontrib>Kong, Mimi</creatorcontrib><creatorcontrib>Zhang, Zhengzheng</creatorcontrib><creatorcontrib>Wang, Qingyi</creatorcontrib><creatorcontrib>Wang, Fangyan</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of diabetes investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Xiaolong</au><au>Liu, Jiaming</au><au>Jin, Keke</au><au>Xu, Haifeng</au><au>Wang, Chuang</au><au>Zhang, Zhuang</au><au>Kong, Mimi</au><au>Zhang, Zhengzheng</au><au>Wang, Qingyi</au><au>Wang, Fangyan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Subcutaneous injection of hydrogen gas is a novel effective treatment for type 2 diabetes</atitle><jtitle>Journal of diabetes investigation</jtitle><addtitle>J Diabetes Investig</addtitle><date>2018-01</date><risdate>2018</risdate><volume>9</volume><issue>1</issue><spage>83</spage><epage>90</epage><pages>83-90</pages><issn>2040-1116</issn><eissn>2040-1124</eissn><abstract>Aims/Introduction
In previous studies, hydrogen gas (H2) administration has clearly shown effectiveness in inhibiting diabetes. Here, we evaluated whether subcutaneous injection of H2 shows enhanced efficacy against type 2 diabetes mellitus induced in mice by a high‐fat diet and low‐dose streptozotocin treatment.
Material and Methods
H2 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 H2 administration.
Results
The bodyweight of H2‐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 H2‐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 H2.
Conclusions
Subcutaneous injection of H2 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 H2 administration.
Subcutaneous injection of H2 significantly improves type 2 diabetes mellitus and DN related outcomes in a mouse model, supporting further consideration of subcutaneous injection as a novel and effective route of clinical H2 administration.</abstract><cop>Japan</cop><pub>John Wiley & Sons, Inc</pub><pmid>28390099</pmid><doi>10.1111/jdi.12674</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-0555-8495</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; DOAJ Directory of Open Access Journals; Wiley Online Library Journals Frontfile Complete; Wiley Online Library Open Access; EZB-FREE-00999 freely available EZB journals; PubMed Central |
subjects | Animals Cholesterol Diabetes Diabetes mellitus Diabetes Mellitus, Experimental - therapy Diabetes Mellitus, Type 2 - complications Diabetes Mellitus, Type 2 - metabolism Diabetes Mellitus, Type 2 - therapy Diabetic Nephropathies - pathology Diabetic Nephropathies - therapy Diabetic nephropathy Diet, High-Fat Fibrosis Glucose tolerance High fat diet Hydrogen Hydrogen - administration & dosage Injection Injections, Subcutaneous Insulin Kidneys Male Mice, Inbred C57BL Nephropathy Original Oxidative Stress Rodents Streptozocin Subcutaneous administration Urine |
title | Subcutaneous injection of hydrogen gas is a novel effective treatment for type 2 diabetes |
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