Mitochondrial dysfunction precedes insulin resistance and hepatic steatosis and contributes to the natural history of non-alcoholic fatty liver disease in an obese rodent model

被引:411
|
作者
Rector, R. Scott [1 ]
Thyfault, John P. [1 ,2 ,3 ,4 ]
Uptergrove, Grace M. [1 ]
Morris, E. Matthew [1 ,3 ,4 ]
Naples, Scott P. [3 ,4 ]
Borengasser, Sarah J. [3 ,4 ]
Mikus, Catherine R. [3 ,4 ]
Laye, Matthew J. [5 ,6 ]
Laughlin, M. Harold [5 ,6 ,7 ,8 ]
Booth, Frank W. [5 ,6 ,7 ,8 ]
Ibdah, Jamal A. [1 ,2 ,5 ,6 ]
机构
[1] Univ Missouri, Div Gastroenterol & Hepatol, Columbia, MO 65212 USA
[2] Harry S Truman Mem Vet Med Ctr, Columbia, MO USA
[3] Univ Missouri, Dept Nutr, Columbia, MO 65212 USA
[4] Univ Missouri, Dept Exercise Physiol, Columbia, MO 65212 USA
[5] Univ Missouri, Dept Med Pharmacol, Columbia, MO 65212 USA
[6] Univ Missouri, Dept Physiol, Columbia, MO 65212 USA
[7] Univ Missouri, Dept Biomed Sci, Columbia, MO 65212 USA
[8] Univ Missouri, Dalton Cardiovasc Res Ctr, Columbia, MO 65212 USA
关键词
Non-alcoholic fatty liver disease; Fatty acid oxidation; Mitochondrial dysfunction; OLETF rat; DIETARY RAT MODEL; UNCOUPLING PROTEIN-2; MUSCLE; ACID; STEATOHEPATITIS; PREVALENCE; ASSOCIATION; EXPRESSION; OXIDATION; CESSATION;
D O I
10.1016/j.jhep.2009.11.030
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: In this study, we sought to determine the temporal relationship between hepatic mitochondrial dysfunction, hepatic steatosis and insulin resistance, and to examine their potential role in the natural progression of non-alcoholic fatty liver disease (NAFLD) utilising a sedentary, hyperphagic, obese, Otsuka Long-Evans Tokushima Fatty (OLETF) rat model. Methods: OLETF rats and their non-hyperphagic control Long-Evans Tokushima Otsuka (LETO) rats were sacrificed at 5, 8, 13, 20, and 40 weeks of age (n = 6-8 per group). Results: At 5 weeks of age, serum insulin and glucose and hepatic triglyceride (TG) concentrations did not differ between animal groups; however, OLETF animals displayed significant (p<0.01) hepatic mitochondrial dysfunction as measured by reduced hepatic carnitine palmitoyl-CoA transferase-1 activity, fatty acid oxidation, and cytochrome c protein content compared with LETO rats. Hepatic TG levels were significantly elevated by 8 weeks of age, and insulin resistance developed by 13 weeks in the OLETF rats. NAFLD progressively worsened to include hepatocyte ballooning, perivenular fibrosis, 2.5-fold increase in serum ALT, hepatic mitochondrial ultrastructural abnormalities, and increased hepatic oxidative stress in the OLETF animals at later ages. Measures of hepatic mitochondrial content and function including beta-hydroxyacyl-CoA dehydrogenase activity, citrate synthase activity, and immunofluorescence staining for mitochondrial carbamoyl phosphate synthetase-1, progressively worsened and were significantly reduced at 40 weeks in OLETF rats compared to LETO animals. Conclusions: Our study documents that hepatic mitochondrial dysfunction precedes the development of NAFLD and insulin resistance in the OLETF rats. This evidence suggests that progressive mitochondrial dysfunction contributes to the natural history of obesity-associated NAFLD. (C) 2010 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:727 / 736
页数:10
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