Nutritional ingredients modulate adipokine secretion and inflammation in human primary adipocytes

Nutrients. 2015 Jan 26;7(2):865-86. doi: 10.3390/nu7020865.

Abstract

Nutritional factors such as casein hydrolysates and long chain polyunsaturated fatty acids have been proposed to exert beneficial metabolic effects. We aimed to investigate how a casein hydrolysate (eCH) and long chain polyunsaturated fatty acids could affect human primary adipocyte function in vitro. Incubation conditions with the different nutritional factors were validated by assessing cell vitality with lactate dehydrogenase (LDH) release and neutral red incorporation. Intracellular triglyceride content was assessed with Oil Red O staining. The effect of eCH, a non-peptidic amino acid mixture (AA), and long-chain polyunsaturated fatty acids (LC-PUFAs) on adiponectin and leptin secretion was determined by enzyme-linked immunosorbent assay (ELISA). Intracellular adiponectin expression and nuclear factor-κB (NF-κB) activation were analyzed by Western blot, while monocyte chemoattractant protein-1 (MCP-1) release was explored by ELISA. The eCH concentration dependently increased adiponectin secretion in human primary adipocytes through its intrinsic peptide bioactivity, since the non-peptidic mixture, AA, could not mimic eCH's effects on adiponectin secretion. Eicosapentaenoic acid (EPA), docosahexaenoic acid (DHA), and DHA combined with arachidonic acid (ARA) upregulated adiponectin secretion. However, only DHA and DHA/ARA exerted a potentanti-inflammatory effect reflected by prevention of tumor necrosis factor-α (TNF-α) induced NF-κB activation and MCP-1 secretion in human adipocytes. eCH and DHA alone or in combination with ARA, may hold the key for nutritional programming through their anti-inflammatory action to prevent diseases with low-grade chronic inflammation such as obesity or diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / drug effects
  • Adipocytes / metabolism*
  • Adipokines / metabolism*
  • Caseins / metabolism*
  • Cell Culture Techniques
  • Chemokine CCL2 / metabolism
  • Docosahexaenoic Acids / metabolism
  • Eicosapentaenoic Acid / metabolism
  • Fatty Acids, Unsaturated / metabolism*
  • Humans
  • Inflammation / metabolism*
  • L-Lactate Dehydrogenase / metabolism
  • Leptin / metabolism
  • Milk Proteins / metabolism*
  • NF-kappa B / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Adipokines
  • CCL2 protein, human
  • Caseins
  • Chemokine CCL2
  • Fatty Acids, Unsaturated
  • Leptin
  • Milk Proteins
  • NF-kappa B
  • Tumor Necrosis Factor-alpha
  • Docosahexaenoic Acids
  • casein hydrolysate
  • Eicosapentaenoic Acid
  • L-Lactate Dehydrogenase