Abstract

Simple SummaryIncreased circulating concentrations of ceramides (Ce) in dairy cows contribute to subcutaneous adipose tissue (SAT) lipolysis and could enhance the risk of developing metabolic disorders. Dietary supply of methionine (Met) or arginine (Arg) alters cellular metabolism in key tissues including SAT. Whether Met or Arg directly affect SAT metabolism when Ce concentrations are elevated is unknown. We propose that Met or Arg could have a beneficial effect within adipose tissue in terms of alleviating potential inflammatory and pro-oxidant effects associated with the transition into lactation.The objective was to perform a proof-of-principle study to evaluate the effects of methionine (Met) and arginine (Arg) supply on protein abundance of amino acid, insulin signaling, and glutathione metabolism-related proteins in subcutaneous adipose tissue (SAT) explants under ceramide (Ce) challenge. SAT from four lactating Holstein cows was incubated with one of the following media: ideal profile of amino acid as the control (IPAA; Lys:Met 2.9:1, Lys:Arg 2:1), increased Met (incMet; Lys:Met 2.5:1), increased Arg (incArg; Lys:Arg 1:1), or incMet plus incArg (Lys:Met 2.5:1 Lys:Arg 1:1) with or without 100 μM exogenous cell-permeable Ce (N-Acetyl-d-sphingosine). Ceramide stimulation downregulated the overall abundance of phosphorylated (p) protein kinase B (AKT), p-mechanistic target of rapamycin (mTOR), and p-eukaryotic elongation factor 2 (eEF2). Without Ce stimulation, increased Met, Arg, or Met + Arg resulted in lower p-mTOR. Compared with control SAT stimulated with Ce, increased Met, Arg, or Met + Arg resulted in greater activation of mTOR (p-mTOR/total mTOR) and AKT (p-AKT/total AKT), with a more pronounced response due to Arg. The greatest protein abundance of glutathione S-transferase Mu 1 (GSTM1) was detected in response to increased Met supply during Ce stimulation. Ceramide stimulation decreased the overall protein abundance of the Na-coupled neutral amino acid transporter SLC38A1 and branched-chain alpha-ketoacid dehydrogenase kinase (BCKDK). However, compared with controls, increased Met or Arg supply attenuated the downregulation of BCKDK induced by Ce. Circulating ceramides might affect amino acid, insulin signaling, and glutathione metabolism in dairy cow adipose tissue. Further in vivo studies are needed to confirm the role of rumen-protected amino acids in regulating bovine adipose function.

Highlights

  • Alterations in subcutaneous adipose tissue (SAT) metabolism are among the key homeorhetic adaptations that characterize the peripartal period in dairy cows [1]

  • Cultures challenged with ceramide, enhanced Met or Arg supply alone or in combination resulted in greater activation of AKT (p-AKT/total AKT) and mechanistic target of rapamycin (mTOR) (p-mTOR/total mTOR) (p < 0.01; p < 0.01; Figures 1C and 2C), with a more pronounced response due to Arg (p < 0.01; Figures 1C and 2C)

  • Compared with IPAA challenged with ceramide, enhanced Met or Arg supply alone or in combination led to lower activation of eukaryotic elongation factor 2 (eEF2) (p-eEF2/total eEF2) (p < 0.01; p < 0.01; p < 0.01; Figure 2F)

Read more

Summary

Introduction

Alterations in subcutaneous adipose tissue (SAT) metabolism are among the key homeorhetic adaptations that characterize the peripartal period in dairy cows [1]. Lipolysis due to decreases in both insulin concentration and sensitivity, along with increased circulating ceramides [2], contributes to the onset of metabolic disorders [3,4,5]. C2:0-ceramide and is a suitable model to study aspects of nutrient metabolism and insulin signaling in bovine SAT. Besides its profound effect on insulin signaling in mammalian cells, downregulation of amino acid (AA) transporters by ceramides could lead to cell death [8]. A lower protein abundance of Na-dependent neutral amino acid transporter 2 (SLC38A2) along with decreased total intracellular AA concentrations were observed in rat L6 myotubes after

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call