High-intensity interval training induces lactylation of fatty acid synthase to inhibit lipid synthesis

The aim of study was to observe the effect of increased lactate levels during high-intensity interval training (HIIT) on protein lactylation, identify the target protein, and investigate the regulatory effect of lactylation on the function of the protein. C57B/L6 mice were divided into 3 groups: the...

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Published in:BMC biology Vol. 21; no. 1; pp. 1 - 196
Main Authors: Chen, Xuefei, Huang, Wenhua, Zhang, Jingbo, Li, Yanjun, Xing, Zheng, Guo, Lanlan, Jiang, Hongfeng, Zhang, Jing
Format: Journal Article
Language:English
Published: London BioMed Central Ltd 19-09-2023
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Summary:The aim of study was to observe the effect of increased lactate levels during high-intensity interval training (HIIT) on protein lactylation, identify the target protein, and investigate the regulatory effect of lactylation on the function of the protein. C57B/L6 mice were divided into 3 groups: the control group, HIIT group, and dichloroacetate injection + HIIT group (DCA + HIIT). The HIIT and DCA + HIIT groups underwent 8 weeks of HIIT treatment, and the DCA + HIIT group was injected DCA before HIIT treatment. The expression of lipid metabolism-related genes was determined. Protein lactylation in subcutaneous adipose tissue was identified and analyzed using 4D label-free lactylation quantitative proteomics and bioinformatics analyses. The fatty acid synthase (FASN) lactylation and activity was determined. HIIT had a significant effect on fat loss; this effect was weakened when lactate production was inhibited. HIIT significantly upregulated the protein lactylation while lactate inhibition downregulated in iWAT. FASN had the most modification sites. Lactate treatment increased FASN lactylation levels, inhibited FASN activity, and reduced palmitate and triglyceride synthesis in 3T3-L1 cells. This investigation revealed that lactate produced by HIIT increased protein pan-lactylation levels in iWAT. FASN lactylation inhibited de novo lipogenesis, which may be an important mechanism in HIIT-induced fat loss.
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ISSN:1741-7007
1741-7007
DOI:10.1186/s12915-023-01698-9