Effects of oral intake of hydrogen water on liver fibrogenesis in mice. Issue 6 (18th June 2013)
- Record Type:
- Journal Article
- Title:
- Effects of oral intake of hydrogen water on liver fibrogenesis in mice. Issue 6 (18th June 2013)
- Main Title:
- Effects of oral intake of hydrogen water on liver fibrogenesis in mice
- Authors:
- Koyama, Yukinori
Taura, Kojiro
Hatano, Etsuro
Tanabe, Kazutaka
Yamamoto, Gen
Nakamura, Kojiro
Yamanaka, Kenya
Kitamura, Koji
Narita, Masato
Nagata, Hiromitsu
Yanagida, Atsuko
Iida, Taku
Iwaisako, Keiko
Fujinawa, Hikohito
Uemoto, Shinji - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="hepr12165-sec-0001" sec-type="section"> <title>Aim</title> <p>Liver fibrosis is the universal consequence of chronic liver diseases. Sustained hepatocyte injury initiates an inflammatory response, thereby activating hepatic stellate cells, the principal fibrogenic cells in the liver. Reactive oxygen species are involved in liver injury and are a promising target for treating liver fibrosis. Hydrogen water is reported to have potential as a therapeutic tool for reactive oxygen species‐associated disorders. This study aimed to investigate the effects of hydrogen water on liver fibrogenesis and the mechanisms underlying these effects.</p> </sec> <sec id="hepr12165-sec-0002" sec-type="section"> <title>Methods</title> <p>C57BL/6 mice were fed with hydrogen water or control water, and subjected to carbon tetrachloride, thioacetamide and bile duct ligation treatments to induce liver fibrosis. Hepatocytes and hepatic stellate cells were isolated from mice and cultured with or without hydrogen to test the effects of hydrogen on reactive oxygen species‐induced hepatocyte injuries or hepatic stellate cell activation.</p> </sec> <sec id="hepr12165-sec-0003" sec-type="section"> <title>Results</title> <p>Oral intake of hydrogen water significantly suppressed liver fibrogenesis in the carbon tetrachloride and thioacetamide models, but these effects were not seen in the bile duct ligation model.<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="hepr12165-sec-0001" sec-type="section"> <title>Aim</title> <p>Liver fibrosis is the universal consequence of chronic liver diseases. Sustained hepatocyte injury initiates an inflammatory response, thereby activating hepatic stellate cells, the principal fibrogenic cells in the liver. Reactive oxygen species are involved in liver injury and are a promising target for treating liver fibrosis. Hydrogen water is reported to have potential as a therapeutic tool for reactive oxygen species‐associated disorders. This study aimed to investigate the effects of hydrogen water on liver fibrogenesis and the mechanisms underlying these effects.</p> </sec> <sec id="hepr12165-sec-0002" sec-type="section"> <title>Methods</title> <p>C57BL/6 mice were fed with hydrogen water or control water, and subjected to carbon tetrachloride, thioacetamide and bile duct ligation treatments to induce liver fibrosis. Hepatocytes and hepatic stellate cells were isolated from mice and cultured with or without hydrogen to test the effects of hydrogen on reactive oxygen species‐induced hepatocyte injuries or hepatic stellate cell activation.</p> </sec> <sec id="hepr12165-sec-0003" sec-type="section"> <title>Results</title> <p>Oral intake of hydrogen water significantly suppressed liver fibrogenesis in the carbon tetrachloride and thioacetamide models, but these effects were not seen in the bile duct ligation model. Treatment of isolated hepatocyte with 1 μg/mL antimycin A generated hydroxyl radicals. Culturing in the hydrogen‐rich medium selectively suppressed the generation of hydroxyl radicals in hepatocytes and significantly suppressed hepatocyte death induced by antimycin A; however, it did not suppress hepatic stellate cell activation.</p> </sec> <sec id="hepr12165-sec-0004" sec-type="section"> <title>Conclusion</title> <p>We conclude that hydrogen water protects hepatocytes from injury by scavenging hydroxyl radicals and thereby suppresses liver fibrogenesis in mice.</p> </sec> </abstract> … (more)
- Is Part Of:
- Hepatology research. Volume 44:Issue 6(2014:Jun.)
- Journal:
- Hepatology research
- Issue:
- Volume 44:Issue 6(2014:Jun.)
- Issue Display:
- Volume 44, Issue 6 (2014)
- Year:
- 2014
- Volume:
- 44
- Issue:
- 6
- Issue Sort Value:
- 2014-0044-0006-0000
- Page Start:
- 663
- Page End:
- 677
- Publication Date:
- 2013-06-18
- Subjects:
- Liver -- Diseases -- Periodicals
Liver Diseases -- Periodicals
Foie -- Maladies -- Périodiques
616.362 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09284346 ↗
http://firstsearch.oclc.org/journal=1386-6346;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1872-034X ↗
http://www.sciencedirect.com/science/journal/13866346 ↗
http://www3.interscience.wiley.com/journal/118507311/home ↗
http://www.blackwell-synergy.com/rd.asp?goto=journal&code=hep ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/hepr.12165 ↗
- Languages:
- English
- ISSNs:
- 1386-6346
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4295.845000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3252.xml