Fatty liver Shionogi-ob/ob mouse: A new candidate for a non-alcoholic steatohepatitis model

被引:17
作者
Sugihara, Takaaki [1 ]
Koda, Masahiko [1 ]
Kishina, Manabu [1 ]
Kato, Jun [1 ]
Tokunaga, Shiho [1 ]
Matono, Tomomitsu [1 ]
Ueki, Masaru [1 ]
Murawaki, Yoshikazu [1 ]
机构
[1] Tottori Univ, Fac Med, Dept Multidisciplinary Internal Med, Div Med & Clin Sci, Yonago, Tottori 6838504, Japan
关键词
apoptosis; fatty liver Shinogi mouse; hepatic fibrosis; Kupffer cell; oxidative stress; NECROSIS-FACTOR-ALPHA; FLS MICE; DISEASE; LEPTIN; EXPRESSION; STRAIN;
D O I
10.1111/j.1872-034X.2012.01101.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Aim The fatty liver Shionogi (FLS) mouse develops hereditary fatty liver without obesity. The FLS-ob/ob mouse made by transferring the leptinob gene demonstrates several metabolic disorders and marked fat deposition in the liver. The aim was to evaluate which mouse model, the FLS or FLS-ob/ob, is more useful for non-alcoholic steatohepatitis research. Methods FLS (n=40) and FLS-ob/ob (n=40) mice were fed a standard diet for 12, 24, 36 and 48 weeks, and then killed. The degree of fat deposition, oxidative stress, fibrosis and apoptosis were analyzed in the liver. Hepatic mRNA expression of fibrogenic and pro-inflammatory cytokines was measured. Results FLS mice developed hepatic steatosis and slight fibrosis without obesity between 12 and 48 weeks of age. Conversely, FLS-ob/ob mice developed severe steatosis at 12 weeks of age, and steatohepatitis with increased oxidative stress and advanced fibrosis between 24 and 36 weeks of age. At 48 weeks of age, some FLS-ob/ob but not FLS mice, progressed to cirrhosis. Transforming growth factor-1, connective tissue growth factor and tumor necrosis factor- mRNA expression levels were greater in FLS-ob/ob than FLS mice between 24 and 48 weeks of age. The number of apoptotic cells in the liver was greater at 12 weeks of age in FLS mice and at 48 weeks of age in FLS-ob/ob mice. Conclusion FLS-ob/ob mice developed more severe steatohepatitis with fibrosis than FLS mice, and had increased oxidative stress and apoptosis. These findings indicate that the FLS-ob/ob mouse is a more useful model for steatohepatitis research.
引用
收藏
页码:547 / 556
页数:10
相关论文
共 27 条
  • [1] Mouse models in non-alcoholic fatty liver disease and steatohepatitis research
    Anstee, QM
    Goldin, RD
    [J]. INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY, 2006, 87 (01) : 1 - 16
  • [2] Infliximab reverses steatosis and improves insulin signal transduction in liver of rats fed a high-fat diet
    Barbuio, Raquel
    Milanski, Marciane
    Bertolo, Manoel B.
    Saad, Mario J.
    Velloso, Licio A.
    [J]. JOURNAL OF ENDOCRINOLOGY, 2007, 194 (03) : 539 - 550
  • [3] Brunt EM, 1999, AM J GASTROENTEROL, V94, P2467, DOI 10.1111/j.1572-0241.1999.01377.x
  • [4] Nonalcoholic fatty liver in Asia: Firmly entrenched and rapidly gaining ground
    Chitturi, Shivakumar
    Wong, Vincent Wai-Sun
    Farrell, Geoff
    [J]. JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2011, 26 : 163 - 172
  • [5] Gene expression of tumor necrosis factor α and TNF-receptors, p55 and p75, in nonalcoholic steatohepatitis patients
    Crespo, J
    Cayón, A
    Fernández-Gil, P
    Hernández-Guerra, M
    Mayorga, M
    Domínguez-Díez, A
    Fernández-Escalante, JC
    Pons-Romero, F
    [J]. HEPATOLOGY, 2001, 34 (06) : 1158 - 1163
  • [6] CHEMOTACTIC ACTIVITY OF THE LIPID-PEROXIDATION PRODUCT 4-HYDROXYNONENAL AND HOMOLOGOUS HYDROXYALKENALS
    CURZIO, M
    ESTERBAUER, H
    DIMAURO, C
    CECCHINI, G
    DIANZANI, MU
    [J]. BIOLOGICAL CHEMISTRY HOPPE-SEYLER, 1986, 367 (04): : 321 - 329
  • [7] Steatohepatitis: A tale of two "hits"?
    Day, CP
    James, OFW
    [J]. GASTROENTEROLOGY, 1998, 114 (04) : 842 - 845
  • [8] Epidemiology of non-alcoholic fatty liver disease in China
    Fan, Jian-Gao
    Farrell, Geoffrey C.
    [J]. JOURNAL OF HEPATOLOGY, 2009, 50 (01) : 204 - 210
  • [9] FOLCH J, 1957, J BIOL CHEM, V226, P497
  • [10] The role of leptin in progression of non-alcoholic fatty liver disease
    Ikejima, K
    Okumura, K
    Lang, T
    Honda, H
    Abe, W
    Yamashina, S
    Enomoto, N
    Takei, Y
    Sato, N
    [J]. HEPATOLOGY RESEARCH, 2005, 33 (02) : 151 - 154