Hepatoprotective effects of fermented Curcuma longa L. on carbon tetrachloride-induced oxidative stress in rats

被引:60
作者
Kim, Yongjae [1 ,2 ]
You, Yanghee [3 ]
Yoon, Ho-Geun [4 ]
Lee, Yoo-Hyun [5 ]
Kim, Kyungmi [6 ]
Lee, Jeongmin [7 ]
Kim, Min Soo [8 ]
Kim, Jong-Choon [9 ]
Jun, Woojin [1 ,3 ]
机构
[1] Chonnam Natl Univ, Div Food & Nutr, Kwangju 550757, South Korea
[2] Korea INS Pharm Res Inst, Jeollanamdo 519822, South Korea
[3] Chonnam Natl Univ, Human Ecol Res Inst, Kwangju 550757, South Korea
[4] Yonsei Univ, Coll Med, Dept Biochem & Mol Biol, Seoul 120752, South Korea
[5] Univ Suwon, Dept Food & Nutr, Suwon 445743, South Korea
[6] Korea Bio Polytech, Dept Biofood Anal, Ganggyung 320905, South Korea
[7] Kyung Hee Univ, Dept Med Nutr, Yongin 446701, South Korea
[8] Chonnam Natl Univ, Dept Stat, Kwangju 550757, South Korea
[9] Chonnam Natl Univ, Coll Vet Med, Kwangju 550757, South Korea
关键词
Fermented Curcuma longa L; Hepatoprotection; Oxidative stress; Antioxidation; Carbon tetrachloride; GREEN TEA EXTRACT; LIVER-INJURY; ANTIOXIDANT; MECHANISMS; DAMAGE; HEPATOTOXICITY; RESVERATROL; FOOD;
D O I
10.1016/j.foodchem.2013.11.058
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The hepatoprotective effect of fermented Curcuma longa L (FC) was investigated in rats under CCl4-induced oxidative stress. FC at a dose of 30 or 300 mg/kg body weight (b.w.) was orally administered for 14 days followed by a single dose of CCl4 (1.25 mL/kg b.w. in 20% corn oil) on day 14. Pretreatment with FC drastically prevented the elevated activities of serum AST, ALT, LDH, and ALP caused by CCl4-induced hepatotoxicity. Histopathologically evident hepatic necrosis was significantly ameliorated by FC pretreatment. When compared to the CCl4-alone treated group, rats pretreated with FC displayed the reduced level of malondialdehyde. Furthermore, FC enhanced antioxidant capacities with higher activities of catalase, glutathione-S-transferase, glutathione reductase, and glutathione peroxidase, and level of reduced glutathione. These results suggest that FC could be a candidate used for the prevention against various liver diseases induced by oxidative stress via elevating antioxidative potentials and decreasing lipid peroxidation. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:148 / 153
页数:6
相关论文
共 35 条
  • [1] Akerboom T P, 1981, Methods Enzymol, V77, P373
  • [2] Oxidative mechanisms in the pathogenesis of alcoholic liver disease
    Albano, Emanuele
    [J]. MOLECULAR ASPECTS OF MEDICINE, 2008, 29 (1-2) : 9 - 16
  • [3] PHARMACOLOGY OF CURCUMA-LONGA
    AMMON, HPT
    WAHL, MA
    [J]. PLANTA MEDICA, 1991, 57 (01) : 1 - 7
  • [4] Role of leptin on alcohol-induced oxidative stress in Swiss mice
    Balasubramaniyan, V
    Sailaja, JK
    Nalini, N
    [J]. PHARMACOLOGICAL RESEARCH, 2003, 47 (03) : 211 - 216
  • [5] Resveratrol and liver disease: from bench to bedside and community
    Bishayee, Anupam
    Darvesh, Altaf S.
    Politis, Themos
    McGory, Robb
    [J]. LIVER INTERNATIONAL, 2010, 30 (08) : 1103 - 1114
  • [6] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [7] CARLBERG I, 1975, J BIOL CHEM, V250, P5475
  • [8] Depression by a Green Tea Extract of Alcohol-Induced Oxidative Stress and Lipogenesis in Rat Liver
    Chen, Kuo-Hsin
    Li, Ping-Chia
    Lin, Wei-Hsiang
    Chien, Chiang-Ting
    Low, Boon-Hua
    [J]. BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2011, 75 (09) : 1668 - 1676
  • [9] Dose- and time-dependent effects of luteolin on carbon tetrachloride-induced hepatotoxicity in mice
    Domitrovic, Robert
    Jakovac, Hrvoje
    Milin, Cedomila
    Radosevic-Stasic, Biserka
    [J]. EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY, 2009, 61 (06) : 581 - 589
  • [10] DRAPER HH, 1990, METHOD ENZYMOL, V186, P421