Omega-3 Fatty Acids Supplementation Differentially Modulates the SDF-1/CXCR-4 Cell Homing Axis in Hypertensive and Normotensive Rats

Nutrients. 2017 Aug 1;9(8):826. doi: 10.3390/nu9080826.

Abstract

Background: We assessed the effect of acute and chronic dietary supplementation of ω-3 on lipid metabolism and cardiac regeneration, through its influence on the Stromal Derived Factor-1 (SDF-1) and its receptor (CXCR4) axis in normotensive and hypertensive rats.

Methods: Male Wistar Kyoto (WKY) and spontaneously hypertensive rats (SHR) were allocated in eight groups (of eight animals each), which received daily orogastric administration of ω-3 (1 g) for 24 h, 72 h or 2 weeks. Blood samples were collected for the analysis of the lipid profile and SDF-1 systemic levels (ELISA). At the end of the treatment period, cardiac tissue was collected for CXCR4 expression analysis (Western blot).

Results: The use of ω-3 caused a reduction in total cholesterol levels (p = 0.044), and acutely activated the SDF-1/CXCR4 axis in normotensive animals (p = 0.037). In the presence of the ω-3, after 72 h, SDF-1 levels decreased in WKY and increased in SHR (p = 0.017), and tissue expression of the receptor CXCR4 was higher in WKY than in SHR (p = 0.001).

Conclusion: The ω-3 fatty acid supplementation differentially modulates cell homing mediators in normotensive and hypertensive animals. While WKY rats respond acutely to omega-3 supplementation, showing increased release of SDF-1 and CXCR4, SHR exhibit a weaker, delayed response.

Keywords: CXCR4 receptor; Stromal Derived Factor-1; Wistar Kyoto rats; cell homing; hypertension; spontaneously hypertensive rats; ω-3 fatty acid.

MeSH terms

  • Animals
  • Blood Pressure / drug effects
  • Chemokine CXCL12 / genetics
  • Chemokine CXCL12 / metabolism*
  • Dietary Supplements
  • Fatty Acids, Omega-3 / pharmacology
  • Gene Expression Regulation / drug effects*
  • Hypertension / physiopathology*
  • Male
  • Rats
  • Rats, Inbred SHR
  • Rats, Inbred WKY
  • Receptors, CXCR4 / genetics
  • Receptors, CXCR4 / metabolism*

Substances

  • CXCL12 protein, rat
  • Chemokine CXCL12
  • Cxcr4 protein, rat
  • Fatty Acids, Omega-3
  • Receptors, CXCR4