4.7 Article

Taurine Attenuates Oxidized Fish Oil-Induced Oxidative Stress and Lipid Metabolism Disorder in Mice

Journal

ANTIOXIDANTS
Volume 11, Issue 7, Pages -

Publisher

MDPI
DOI: 10.3390/antiox11071391

Keywords

oxidized fish oil; taurine; liver injury; oxidative stress; lipid metabolism

Funding

  1. National Key R&D Program of China [2021YFD1300403]
  2. National Nature Science Foundation of China [32102572]
  3. Open Fund of Key Laboratory of Agro-ecological Processes in Subtropical Region, Chinese Academy of Sciences [ISA2021202]
  4. Changsha Natural Science Funds for Distinguished Young Scholar [kq2009020]
  5. Young Elite Scientists Sponsorship Program by CAST [2020-2022QNRC003]
  6. Earmarked Fund for China Agriculture Research System [CARS-35]

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The objective of this study was to investigate the effect of dietary taurine on lipid metabolism and liver injury in mice fed a diet high in oxidized fish oil. The results showed that dietary taurine could ameliorate liver injury and lipid metabolism disorder caused by the oxidized fish oil diet. Taurine supplementation improved liver function, reduced lipid levels in serum, and increased the expression of genes related to lipid metabolism in the liver. Furthermore, impaired autophagy flux caused by the oxidized fish oil diet was prevented by taurine.
The objective of this study was to determine the effect of dietary taurine on lipid metabolism and liver injury in mice fed a diet high in oxidized fish oil. The ICR mice (six weeks old) were randomly assigned to six groups and fed different diets for 10 weeks: control (CON), normal plus 15% fresh fish oil diet (FFO), normal plus 15% oxidized fish oil diet (OFO), or OFO plus 0.6% (TAU1), 0.9% (TAU2) or 1.2% (TAU3) taurine. Compared to the CON group, OFO mice showed increased liver index, aspartate aminotransferase (AST) and malondialdehyde (MDA) levels in serum (p < 0.05). In addition, OFO mice had increased cholesterol (CHOL)/high-density lipoprotein cholesterol (HDL-C) and decreased HDL-C/low-density lipoprotein cholesterol (LDL-C) and n-6/n-3 polyunsaturated fatty acid (PUFA) ratio in serum (p < 0.05) compared with CON mice. Notably, dietary taurine ameliorated the liver index and AST and MDA levels in serum and liver in a more dose-dependent manner than OFO mice. In addition, compared to OFO mice, decreased levels of CHOL and ratio of CHOL/HDL-C and n-6 PUFA/n-3 PUFA in serum were found in TAU3-fed mice. Supplementation with TAU2 and TAU3 increased the relative mRNA expression levels of peroxisome proliferator-activated receptor alpha, adipose triglyceride lipase, lipoprotein lipase, hormone-sensitive lipase and carnitine palmitoyl transferase 1 in liver compared with the OFO group (p < 0.05). Moreover, impaired autophagy flux was detected in mice fed with the OFO diet, and this was prevented by taurine. These findings suggested that dietary taurine might provide a potential therapeutic choice against oxidative stress and lipid metabolism disorder.

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