The Protective Effect of ENA Actimineral Resource A on CCl4-Induced Liver Injury in Rats

被引:7
作者
Hong, Il-Hwa [1 ]
Ji, Hoon [1 ]
Hwa, Sung-Yong [2 ]
Jeong, Won-Il [1 ]
Jeong, Da-Hee [1 ]
Do, Sun-Hee [3 ]
Kim, Ji-Min [4 ]
Ki, Mi-Ran [1 ]
Park, Jin-Kyu [1 ]
Goo, Moon-Jung [1 ]
Hwang, Ok-Kyung [1 ]
Hong, Kyung-Sook [1 ]
Han, Jung-Youn [1 ]
Chung, Hae-Young [4 ]
Jeong, Kyu-Shik [1 ]
机构
[1] Kyungpook Natl Univ, Dept Pathol, Coll Vet Med, Taegu 702701, South Korea
[2] Jinju Bio Food, Jinju 660931, South Korea
[3] Konkuk Univ, Dept Clin Pathol, Coll Vet Med, Seoul 143701, South Korea
[4] Pusan Natl Univ, Longev Life Sci & Technol Inst, Dept Pharm, Pusan 609735, South Korea
关键词
ENA actimineral resource A; Antioxidant capability; Hepatoxicity; Seaweed; Carbon tetrachloride; CARBON-TETRACHLORIDE; IN-VIVO; LIPID-PEROXIDATION; OXIDATIVE STRESS; GENE-EXPRESSION; ENZYMES; METABOLISM; KININOGEN; PHASE; NRF2;
D O I
10.1007/s10126-010-9317-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
ENA Actimineral Resource A (ENA-A) is alkaline water that is composed of refined edible cuttlefish bone and two different species of seaweed, Phymatolithon calcareum and Lithothamnion corallioides. In the present study, ENA-A was investigated as an antioxidant to protect against CCl4-induced oxidative stress and hepatotoxicity in rats. Liver injury was induced by either subacute or chronic CCl4 administration, and the rats had free access to tap water mixed with 0% (control group) or 10% (v/v) ENA-A for 5 or 8 weeks. The results of histological examination and measurement of antioxidant activity showed that the reactive oxygen species production, lipid peroxidation, induction of CYP2E1 were decreased and the antioxidant activity, including glutathione and catalase production, was increased in the ENA-A groups as compared with the control group. On 2-DE gel analysis of the proteomes, 13 differentially expressed proteins were obtained in the ENA-A groups as compared with the control group. Antioxidant proteins, including glutathione S-transferase, kelch-like ECH-associated protein 1, and peroxiredoxin 1, were increased with hepatocyte nuclear factor 3-beta and serum albumin precursor, and kininogen precursor decreased more in the ENA-A groups than compared to the control group. In conclusion, our results suggest that ENA-A does indeed have some protective capabilities against CCl4-induced liver injury through its antioxidant function.
引用
收藏
页码:462 / 473
页数:12
相关论文
共 46 条
[1]  
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[2]   Liver cirrhosis and metabolism (sugar, protein, fat and trace elements) [J].
Arakawa, Y ;
Moriyama, M ;
Arakawa, Y .
HEPATOLOGY RESEARCH, 2004, 30 :S46-S58
[3]  
ARAKAWA Y, 2003, LIVER DIS BIOELEMENT, V1, P1
[4]   HEPATOPROTECTIVE ACTIVITY OF CARROT (DAUCUS-CAROTA L) AGAINST CARBON-TETRACHLORIDE INTOXICATION IN MOUSE-LIVER [J].
BISHAYEE, A ;
SARKAR, A ;
CHATTERJEE, M .
JOURNAL OF ETHNOPHARMACOLOGY, 1995, 47 (02) :69-74
[5]   Hepatocyte-specific ablation of Foxa2 alters bile acid homeostasis and results in endoplasmic reticulum stress [J].
Bochkis, Irina M. ;
Rubins, Nir E. ;
White, Peter ;
Furth, Emma E. ;
Friedman, Joshua R. ;
Kaestner, Klaus H. .
NATURE MEDICINE, 2008, 14 (08) :828-836
[6]   Overoxidation of peroxiredoxins as an immediate and sensitive marker of oxidative stress in HepG2 cells and its application to the redox effects induced by ischemia/reperfusion in human liver [J].
Cesaratto, L ;
Vascotto, C ;
D'Ambrosio, CR ;
Scaloni, A ;
Baccarani, U ;
Paron, I ;
Damante, G ;
Calligaris, S ;
Quadrifoglio, F ;
Tiribelli, C ;
Tell, G .
FREE RADICAL RESEARCH, 2005, 39 (03) :255-268
[7]   Characterization of three isoforms of mammalian peroxiredoxin that reduce peroxides in the presence of thioredoxin [J].
Chae, HZ ;
Kim, HJ ;
Kang, SW ;
Rhee, SG .
DIABETES RESEARCH AND CLINICAL PRACTICE, 1999, 45 (2-3) :101-112
[8]   MAJOR ACUTE PHASE ALPHA-1-PROTEIN OF THE RAT IS HOMOLOGOUS TO BOVINE KININOGEN AND CONTAINS THE SEQUENCE FOR BRADYKININ - ITS SYNTHESIS IS REGULATED AT THE MESSENGER-RNA LEVEL [J].
COLE, T ;
INGLIS, AS ;
ROXBURGH, CM ;
HOWLETT, GJ ;
SCHREIBER, G .
FEBS LETTERS, 1985, 182 (01) :57-61
[9]   Transcription factors in liver development, differentiation, and regeneration [J].
Costa, RH ;
Kalinichenko, VV ;
Holterman, AXL ;
Wang, XH .
HEPATOLOGY, 2003, 38 (06) :1331-1347
[10]   MULTIPLE HEPATOCYTE-ENRICHED NUCLEAR FACTORS FUNCTION IN THE REGULATION OF TRANSTHYRETIN AND ALPHA-1-ANTITRYPSIN GENES [J].
COSTA, RH ;
GRAYSON, DR ;
DARNELL, JE .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (04) :1415-1425