Key result
High-dose NEFAs activate TLR4 inflammatory signaling and reduce insulin sensitivity in vitro.
Why the study?
The relationship between negative energy balance, insulin resistance, and inflammation in dairy cows during the perinatal period was unclear.
Do nonesterified fatty acids (NEFAs) influence the NF-κB inflammatory and insulin signaling pathways through TLR4 in bovine hepatocytes?
Do nonesterified fatty acids (NEFAs) influence the NF-κB inflammatory and insulin signaling pathways through TLR4 in bovine hepatocytes?
p-value: p=<0.05
High-dose NEFAs induce inflammation and insulin resistance in bovine hepatocytes via the TLR4 pathway, providing mechanistic insight into perinatal metabolic diseases in dairy cows.
In vitro bovine data suggest NEFA-TLR4 links to insulin resistance; leaves open in vivo or clinical translation.
Dairy cows are often in a state of negative energy balance (NEB), because of decreased dry matter intake and increased energy requirements, initiating lipid mobilization and leading to high serum β-hydroxybutyrate and nonesterified fatty acid (NEFA) levels, which can induce ketosis and fatty liver in dairy cows. We all have known that inflammation and insulin resistance are also common diseases in perinatal period of dairy cows. So what is the relationship between negative energy balance, insulin resistance and inflammation in cow? In order to study the role of NEFAs in the NF-κB inflammatory and insulin signaling pathways through TLR4, we cultured bovine primary hepatocytes and added different concentrations of NEFAs to test the mRNA and protein levels of inflammatory and insulin signaling pathways. Our experiments indicated that NEFAs could activate the NF-κB 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 can activate the TLR4/NF-κB inflammatory signaling pathway, and reduce the sensitivity of the insulin pathway through the TLR4/PI3K/AKT metabolic axis.
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Deng et al. (2021) studied Ketosis and fatty liver in dairy cows (in vitro model). Nonesterified fatty acids (NEFAs) vs. DMSO or blank control was evaluated on Protein and mRNA levels of inflammatory and insulin signaling pathways (p=<0.05). High-dose NEFAs activated the TLR4/NF-κB inflammatory signaling pathway and reduced the sensitivity of the insulin pathway through the TLR4/PI3K/AKT metabolic axis in bovine hepatocytes in vitro.
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