Effects of sn-2 Palmitic Triacylglycerols and the Ratio of OPL to OPO in Human Milk Fat Substitute on Metabolic Regulation in Sprague-Dawley Rats

Nutrients. 2024 Apr 26;16(9):1299. doi: 10.3390/nu16091299.

Abstract

In this study, the influence of total sn-2 palmitic triacylglycerols (TAGs) and ratio of 1-oleoyl-2-palmitoyl-3-linoleoylglycerol (OPL) to 1,3-dioleoyl-2-palmitoylglycerol (OPO) in human milk fat substitute (HMFS) on the metabolic changes were investigated in Sprague-Dawley rats. Metabolomics and lipidomics profiling analysis indicated that increasing the total sn-2 palmitic TAGs and OPL to OPO ratio in HMFS could significantly influence glycine, serine and threonine metabolism, glycerophospholipid metabolism, glycerolipid metabolism, sphingolipid metabolism, bile acid biosynthesis, and taurine and hypotaurine metabolism pathways in rats after 4 weeks of feeding, which were mainly related to lipid, bile acid and energy metabolism. Meanwhile, the up-regulation of taurine, L-tryptophan, and L-cysteine, and down-regulations of lysoPC (18:0) and hypoxanthine would contribute to the reduction in inflammatory response and oxidative stress, and improvement of immunity function in rats. In addition, analysis of targeted biochemical factors also revealed that HMFS-fed rats had significantly increased levels of anti-inflammatory factor (IL-4), immunoglobulin A (IgA), superoxide dismutase (SOD), and glutathione peroxidase (GSH-px), and decreased levels of pro-inflammatory factors (IL-6 and TNF-α) and malondialdehyde (MDA), compared with those of the control fat-fed rats. Collectively, these observations present new in vivo nutritional evidence for the metabolic regulatory effects of the TAG structure and composition of human milk fat substitutes on the host.

Keywords: human milk fat substitute; lipidomics; metabolomics; sn-2 palmitic triacylglycerols.

MeSH terms

  • Animals
  • Fat Substitutes* / pharmacology
  • Female
  • Glycerides / metabolism
  • Glycerides / pharmacology
  • Humans
  • Lipid Metabolism / drug effects
  • Lipidomics
  • Male
  • Metabolomics / methods
  • Milk, Human* / chemistry
  • Oxidative Stress / drug effects
  • Rats
  • Rats, Sprague-Dawley*
  • Triglycerides* / metabolism

Substances

  • Triglycerides
  • Fat Substitutes
  • Glycerides

Grants and funding

This work was supported by a grant from the Wilmar (Shanghai) Biotechnology Research and Development Center Co., Ltd.