Threonine modulates the STAT3-SCD1 pathway to reduce fatty acid metabolism in duck hepatocytes.

Poult Sci

Key Laboratory for Animal Genetics & Molecular Breeding of Jiangsu Province, College of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China. Electronic address:

Published: December 2024

AI Article Synopsis

  • Dietary threonine (Thr) affects fat storage in ducks, possibly by regulating hepatic lipid metabolism through the STAT3 protein.
  • Research involved isolating duck liver cells and treating them with various doses of Thr or a STAT3 overexpression plasmid to study fatty acid and triglyceride levels.
  • Findings showed that both Thr and overexpressed STAT3 reduce fat deposition in liver cells by inhibiting specific fatty acid and triglyceride metabolism pathways, particularly targeting the SCD1 gene.

Article Abstract

Dietary threonine (Thr) is known to influence fat deposition in poultry, but the precise mechanisms behind its regulatory effects on hepatic lipid metabolism remain elusive. Prior research indicated that including supplemental Thr in the feed may influence STAT3 (Signal Transducer and Activator of Transcription 3) levels in the liver of meat ducks. Numerous studies have recorded the function of STAT3 in regulating fatty acid (FA) metabolism in mammals. The primary objective of this study was to investigate whether Thr influences FA metabolism and triglycerides (TG) deposition in duck liver by regulating STAT3 expression. Primary hepatocytes were isolated from duck embryos and treated for 36 h with different doses of Thr (0, 10, 25, 50, 200 μM) in vitro or with a constructed STAT3 overexpression plasmid to examine the content of FAs and TG. RNA-seq was used to detect changes in gene expression in hepatocytes following STAT3 overexpression. The results demonstrated that both the exogenous addition of Thr and the overexpression of STAT3 significantly suppressed the capacity of hepatocytes for FAs deposition (P < 0.05). The overexpression of STAT3 also inhibited TG accumulation under conditions in response to Thr deficiency (P < 0.01). Transcriptomic analyses indicated that the overexpression of STAT3 inhibits the activity of triglyceride metabolism and unsaturated fatty acid biosynthesis (P < 0.01). Finally, a dual-luciferase reporter test demonstrated that STAT3 may systematically target and inhibit SCD1 transcription (P < 0.01). The present study indicates that supplemental Thr (50 μM) inhibits hepatic FA deposition via the STAT3-SCD1 pathway. This work enhances our comprehension of the functional roles of Thr and STAT3 in modulating lipid metabolism within duck livers. Moreover, it provides a partial theoretical foundation for the nutritional prevention and pharmacological intervention of lipid metabolism disorders in poultry.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11564961PMC
http://dx.doi.org/10.1016/j.psj.2024.104444DOI Listing

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