4.7 Article

Mitochondrial Dysfunction in Obesity-Associated Nonalcoholic Fatty Liver Disease: The Protective Effects of Pomegranate with Its Active Component Punicalagin

期刊

ANTIOXIDANTS & REDOX SIGNALING
卷 21, 期 11, 页码 1557-1570

出版社

MARY ANN LIEBERT, INC
DOI: 10.1089/ars.2013.5538

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资金

  1. National Natural Science Foundation of China [81201023, 31370844]
  2. 973 program for young scientists [2014CB548200]
  3. Tianjin Applied Basic and Frontier Tech Major Project [12JCZDJC34400]
  4. Tianjin higher Education Sci-tech Development Project [20112D05]
  5. UC Davis Center for Human and Nutrition Pilot Award [CHNR08-318]
  6. National Twelfth Five-Year Plan for Science Sc. Technology Support [2012BAH30F03]
  7. Fundamental Research Funds for the Central Universities
  8. Xi'an Jiaotong University
  9. Nestle Research Center, Switzerland

向作者/读者索取更多资源

Aims: Punicalagin (PU) is one of the major ellagitannins found in the pomegranate (Punica granatuni), which is a popular fruit with several health benefits. So far, no studies have evaluated the effects of PU on nonalcoholic fatty liver disease (NAFLD). Our work aims at studying the effect of PU-enriched pomegranate extract (PE) on high fat diet (HFD)-induced NAFLD. Results: PE administration at a dosage of 150 mg/kg/day significantly inhibited HFD-induced hyperhpidemia and hepatic lipid deposition. As major contributors to NAFLD, increased expression of pro-inflammatory cytokines such as tumor necrosis factor-alpha, interleukins 1, 4, and 6 as well as augmented oxidative stress in hepatocytes followed by nuclear factor (erythroid-derived-2)-like 2 (Nrf2) activation were normalized through PE supplementation. In addition, PE treatment reduced uncoupling protein 2 (UCP2) expression, restored ATP content, suppressed mitochondrial protein oxidation, and improved mitochondrial complex activity in the liver. In contrast, mitochondrial content was not affected despite increased peroxisomal proliferator-activated receptor gamma coactivator-la (PGC-1 alpha) and elevated expression of genes related to mitochondrial beta-oxidation after PE treatment. Finally, PU was identified as the predominant active component of PE with regard to the lowering of triglyceride and cholesterol content in HepG2 cells, and both PU- and PE-protected cells from palmitate induced mitochondria dysfunction and insulin resistance. Innovation: Our work presents the beneficial effects of PE on obesity-associated NAFLD and multiple risk factors. PU was proposed to be the major active component. Conclusions: By promoting mitochondrial function, eliminating oxidative stress and inflammation, PU may be a useful nutrient for the treatment of NAFLD.

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