4.7 Article

NEFAs Influence the Inflammatory and Insulin Signaling Pathways Through TLR4 in Primary Calf Hepatocytes in vitro

期刊

FRONTIERS IN VETERINARY SCIENCE
卷 8, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fvets.2021.755505

关键词

NEFAs; insulin resistance; NF-kappa B signaling pathway; lipid metabolism; bovine hepatocytes

资金

  1. National Natural Science Foundation of China (Beijing, China) [31602121, 31760752]
  2. Young Scientific and Technological Talents in Inner Mongolia (Inner Mongolia, China) [NJYT-20-B30]
  3. Natural Science Foundation of Inner Mongolia (Inner Mongolia, China) [2021LHMS03009]
  4. Inner Mongolia Beef Diseases Prevention and Control Engineering Technology Research Center [MDK2019023]
  5. Inner Mongolia University for Nationalities [BS476]

向作者/读者索取更多资源

Transition dairy cows often experience negative energy balance, insulin resistance, and inflammation. NEFAs can activate the NF-kappa B inflammatory signaling pathway through TLR4, influencing insulin resistance. Inhibitors of TLR4 can alleviate the inhibitory effects of NEFAs and reduce the activation of the inflammatory signaling pathway.
Transition dairy cows are often in a state of negative energy balance because of decreased dry matter intake and increased energy requirements, initiating lipid mobilization and leading to high serum beta-hydroxybutyrate (BHBA) and non-esterified fatty acid (NEFAs) levels, which can induce ketosis and fatty liver in dairy cows. Inflammation and insulin resistance are also common diseases in the perinatal period of dairy cows. What is the relationship between negative energy balance, insulin resistance and inflammation in dairy cows? To study the role of non-esterified fatty acids in the nuclear factor kappa beta (NF-kappa B) inflammatory and insulin signaling pathways through Toll-like receptor 4 (TLR4), we cultured primary calf hepatocytes and added different concentrations of NEFAs to assess the mRNA and protein levels of inflammatory and insulin signaling pathways. Our experiments indicated that NEFAs could activate the NF-kappa B inflammatory signaling pathway and influence insulin resistance through TLR4. However, an inhibitor of TLR4 alleviated the inhibitory effects of NEFAs on the insulin pathway. In conclusion, all of these results indicate that high-dose NEFAs (2.4 mM) can activate the TLR4/NF-kappa B inflammatory signaling pathway and reduce the sensitivity of the insulin pathway through the TLR4/PI3K/AKT metabolic axis.

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