4.6 Article

The Hepatotoxicity of Palmitic Acid in Zebrafish Involves the Intestinal Microbiota

期刊

JOURNAL OF NUTRITION
卷 148, 期 8, 页码 1217-1228

出版社

OXFORD UNIV PRESS
DOI: 10.1093/jn/nxy084

关键词

palmitic acid; lipotoxicity; liver damage; ER stress; gut microbiota

资金

  1. Key Project of the National Science and Technology Support Program Project of China [2014CB138600]
  2. Beijing earmarked fund for the Modern Agro-industry Technology Research System [SCGWZJ20151104-4]
  3. Key Project of the Chinese National Programs for Fundamental Research and Development [2015CB150605]
  4. National Natural Science Foundation of China [31272672, 31572633]
  5. Fundamental Research Funds for the Central Public Welfare Research Institute [1610382016013]
  6. National Genetically Modified Project of China [2016ZX08011-005]

向作者/读者索取更多资源

Background: Palmitic acid (PA) is the main saturated fatty acid naturally occurring in animal fats and vegetable oils. In recent decades, palm oil, an alternative lipid source containing high amounts of PA, has been widely used to replace fish oil in aquafeed. Objective: We investigated the hepatotoxicity of PA in zebrafish and the underlying mechanism. Methods: One-month-old zebrafish fed a high-fat diet (HFD) containing 16% soybean oil and 3 PA-incorporated HFDs [4%, 8%, and 12% PA (12PA)] for 2 wk (experiment 1) and 4 wk (experiment 2) were used to evaluate PA-induced liver damage and endoplasmic reticulum (ER) stress. Germ-free (GF) zebrafish fed low-fat, high-fat, or 12PA diets for 5 d were used to study the direct effects of PA on liver damage (experiment 3). GF zebrafish colonized with HFD or 12PA microbiota for 48 h were used to elucidate the indirect effects of PA-altered microbiota on liver damage (experiment 4). Last, GF zebrafish colonized with HFD or 12PA microbiota were used to evaluate the effects of different microbiotas on PA absorption (experiment 5). Results: In experiment 1, the proportion of PA in the liver linearly increased as its percentage in dietary lipid increased (r(2) = 0.83, P < 0.05). In experiment 2, the expression of glucose-regulated protein 78 (Grp78) and C/EBP-homologous protein (Chop) was higher in the 12PA group than in the HFD group (2.2-and 2.7-fold, respectively; P < 0.05). The activity of caspase-12 was increased by 61.1% in the 12PA group compared with the HFD group (P < 0.05). In experiment 3, caspase-12 activity was higher in the 12PA group than in the HFD group (P < 0.05). In experiment 4, GF zebrafish colonized with PA-altered microbiota had higher caspase-12 activity (P < 0.05) than those colonized by HFD microbiota. In experiment 5, PA-altered microbiota promoted PA absorption (P < 0.05) and aggravated ER stress and liver damage in the context of high-PA feeding. Conclusions: The PA-altered microbiota indirectly induced ER stress and liver damage in zebrafish. Moreover, the PA microbiota promoted the absorption of PA, leading to enhanced PA overflow into the liver and aggravated hepatotoxicity of PA in zebrafish.

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