Hepatoprotection of Noni Juice against Chronic Alcohol Consumption: Lipid Homeostasis, Antioxidation, Alcohol Clearance, and Anti-inflammation

被引:56
作者
Chang, Yuan-Yen [1 ,2 ,3 ]
Lin, Yi-Ling [4 ]
Yang, Deng-Jye [5 ]
Liu, Chen-Wei [6 ,7 ]
Hsu, Chin-Lin [8 ]
Tzang, Bor-Show [4 ]
Chen, Yi-Chen [9 ]
机构
[1] Chung Shan Med Univ, Sch Med, Dept Microbiol & Immunol, Taichung 402, Taiwan
[2] Chung Shan Med Univ, Sch Med, Inst Microbiol & Immunol, Taichung 402, Taiwan
[3] Chung Shan Med Univ Hosp, Dept Med Educ, Taichung 402, Taiwan
[4] Chung Shan Med Univ, Inst Biochem & Biotechnol, Taichung 402, Taiwan
[5] Chung Shan Med Univ, Sch Hlth Diet & Ind Management, Taichung 402, Taiwan
[6] Ming Dao Univ, Dept Postmodern Agr, Changhua 523, Taiwan
[7] Ming Dao Univ, Dept Biotechnol, Changhua 523, Taiwan
[8] Chung Shan Med Univ, Sch Nutr, Taichung 402, Taiwan
[9] Natl Taiwan Univ, Dept Anim Sci & Technol, Taipei 106, Taiwan
关键词
alcohol metabolism; anti-inflammatory response; antioxidant capacity; lipid homeostasis; noni juice; MORINDA-CITRIFOLIA NONI; FAT/CHOLESTEROL-DIETARY HAMSTERS; INDUCED LIVER-INJURY; FATTY LIVER; TNF-ALPHA; L; JUICE; RATS; ACTIVATION; ACETALDEHYDE; GLYCOSIDES;
D O I
10.1021/jf4038419
中图分类号
S [农业科学];
学科分类号
082806 [农业信息与电气工程];
摘要
Chronic alcohol consumption leads to steatohepatitis and cirrhosis. Naturally fermented noni juice (NJ) contains polyphenols, polysaccharides, and some trace minerals. This study explored protective effects of NJ against chronic alcohol consumption. Mice were assigned randomly to one of the following groups: (1) control, control liquid diet and distilled water; (2) alcohol, alcohol liquid diet and distilled water; (3) Alc+NJ_IX, alcohol liquid diet and 5 mL NJ/kg BW; (4) Alc+NJ_2X, alcohol liquid diet and 10 mL NJ/kg BW; (5) Alc+NJ_3X, alcohol and 15 mL NJ/kg BW for 4 weeks. NJ decreased (p < 0.05) serum AST, ALT, and alcohol levels and liver lipids, as well as increased (p < 0.05) daily fecal lipid outputs in alcohol-diet fed mice. NJ supplementation not only down-regulated (p < 0.05) lipogenesis but also up-regulated (p < 0.05) fatty acid beta-oxidation in livers of alcohol-diet fed mice. NJ also accelerated alcohol clearance via increased (p < 0.05) hepatic ADH and ALDH activities. NJ increased (p < 0.05) hepatic TEAC and GSH levels but decreased (p < 0.05) TBARS value and TLR2/4, P38, ERK 1/2, NF kappa B P65, iNOS, COX-2, TNF-alpha, and IL-1 beta expressions in alcohol-diet fed mice. NJ promotes hepatoprotection against alcohol-induced injury due to regulations of lipid homeostasis, antioxidant status, alcohol metabolism, and anti-inflammatory responses.
引用
收藏
页码:11016 / 11024
页数:9
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