Protein Digests and Pure Peptides from Chia Seed Prevented Adipogenesis and Inflammation by Inhibiting PPARγ and NF-κB Pathways in 3T3L-1 Adipocytes

Nutrients. 2021 Jan 8;13(1):176. doi: 10.3390/nu13010176.

Abstract

The objective was to evaluate the mechanisms of digested total proteins (DTP), albumin, glutelin, and pure peptides from chia seed (Salvia hispanica L.) to prevent adipogenesis and its associated inflammation in 3T3-L1 adipocytes. Preadipocytes (3T3-L1) were treated during differentiation with either DTP or digested albumin or glutelin (1 mg/mL) or pure peptides NSPGPHDVALDQ and RMVLPEYELLYE (100 µM). Differentiated adipocytes also received DTP, digested albumin or glutelin (1 mg/mL), before (prevention) or after (inhibition) induced inflammation by addition of conditioned medium (CM) from inflamed macrophages. All treatments prevented adipogenesis, reducing more than 50% the expression of PPARγ and to a lesser extent lipoprotein lipase (LPL), fatty acid synthase (FAS), sterol regulatory element-binding protein 1 (SREBP1), lipase activity and triglycerides. Inflammation induced by CM was reduced mainly during prevention, while DTP decreased expression of NF-κB (-48.4%), inducible nitric oxide synthase (iNOS) (-46.2%) and COX-2 (-64.5%), p < 0.05. Secretions of nitric oxide, PGE2 and TNFα were reduced by all treatments, p < 0.05. DTP reduced expressions of iNOS (-52.1%) and COX-2 (-66.4%). Furthermore, digested samples and pure peptides prevented adipogenesis by modulating PPARγ and additionally, preventing and even inhibiting inflammation in adipocytes by inhibition of PPARγ and NF-κB expression. These results highlight the effectiveness of digested total proteins and peptides from chia seed against adipogenesis complications in vitro.

Keywords: Salvia hispanica L.; adipocytes; bioactive peptides; digested proteins; inflammation; obesity.

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / drug effects
  • Adipocytes / immunology
  • Adipocytes / physiology*
  • Adipogenesis / drug effects*
  • Albumins / pharmacology
  • Animals
  • Fatty Acid Synthases / metabolism
  • Glutens / pharmacology
  • Inflammation / prevention & control*
  • Lipid Metabolism
  • Mice
  • Monoacylglycerol Lipases / metabolism
  • NF-kappa B / metabolism
  • PPAR gamma / metabolism
  • Peptides / pharmacology*
  • Plant Proteins / pharmacology*
  • RAW 264.7 Cells
  • Salvia / chemistry*
  • Seed Storage Proteins / pharmacology
  • Seeds / chemistry*
  • Signal Transduction / drug effects

Substances

  • Albumins
  • NF-kappa B
  • PPAR gamma
  • Peptides
  • Plant Proteins
  • Seed Storage Proteins
  • Glutens
  • Fatty Acid Synthases
  • Monoacylglycerol Lipases