Anti-oxidant and anti-inflammatory effects of hydrogen-rich water alleviate ethanol-induced fatty liver in mice

被引:41
作者
Lin, Ching-Pin [1 ,2 ]
Chuang, Wen-Chen [3 ]
Lu, Fung-Jou [3 ]
Chen, Chih-Yen [4 ,5 ]
机构
[1] Chung Shan Med Univ, Inst Biochem Microbiol & Immunol, Taichung 402, Taiwan
[2] Chung Shan Med Univ Hosp, Dept Internal Med, Div Gastroenterol, Taichung 402, Taiwan
[3] Chung Shan Med Univ, Inst Med, Taichung 402, Taiwan
[4] Taipei Vet Gen Hosp, Dept Med, Div Gastroenterol & Hepatol, 201,Sec 2,Shih Pai Rd, Taipei 112, Taiwan
[5] Natl Yang Ming Univ, Sch Med, Fac Med, Taipei 112, Taiwan
关键词
hydrogen; chronic plus binge EtOH feeding; antioxidant; protective cytokine; acyl ghrelin; female mice; ELECTROLYZED-REDUCED WATER; OXIDATIVE STRESS; MOLECULAR-HYDROGEN; GHRELIN; INTERLEUKIN-10; DISEASE; SALINE; MODEL; STEATOHEPATITIS; INFLAMMATION;
D O I
10.3748/wjg.v23.i27.4920
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM To investigate the effects of hydrogen-rich water (HRW) treatment on prevention of ethanol (EtOH)-induced early fatty liver in mice. METHODS In vitro reduction of hydrogen peroxide by HRW was determined with a chemiluminescence system. Female mice were randomly divided into five groups: control, EtOH, EtOH + silymarin, EtOH + HRW and EtOH + silymarin + HRW. Each group was fed a Lieber-DeCarli liquid diet containing EtOH or isocaloric maltose dextrin (control diet). Silymarin was used as a positive control to compare HRW efficacy against chronic EtOH-induced hepatotoxicity. HRW was freshly prepared and given at a dosage of 1.2 mL/mouse trice daily. Blood and liver tissue were collected after chronic-binge liquid-diet feeding for 12 wk. RESULTS The in vitro study showed that HRW directly scavenged hydrogen peroxide. The in vivo study showed that HRW increased expression of acyl ghrelin, which was correlated with food intake. HRW treatment significantly reduced EtOH-induced increases in serum alanine aminotransferase, aspartate aminotransferase, triglycerol and total cholesterol levels, hepatic lipid accumulation and inflammatory cytokines, including tumor necrosis factor-alpha (TNF-alpha) and interleukin (IL)-6. HRW attenuated malondialdehyde level, restored glutathione depletion and increased superoxide dismutase, glutathione peroxidase and catalase activities in the liver. Moreover, HRW reduced TNF-alpha and IL-6 levels but increased IL-10 and IL-22 levels. CONCLUSION HRW protects against chronic EtOH-induced liver injury, possibly by inducing acyl ghrelin to suppress the pro-inflammatory cytokines TNF-alpha and IL-6 and induce IL-10 and IL-22, thus activating antioxidant enzymes against oxidative stress.
引用
收藏
页码:4920 / 4934
页数:15
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