Grape juice attenuates left ventricular hypertrophy in dyslipidemic mice

PLoS One. 2020 Sep 3;15(9):e0238163. doi: 10.1371/journal.pone.0238163. eCollection 2020.

Abstract

Objective: We evaluated the effects of grape juice (Vitis labrusca L.) on dyslipidemia, resistance to insulin, and left ventricular hypertrophy (LVH) in mice homozygous for the absence of the LDL receptor gene (LDLr -/-) under a hyperlipidemic diet.

Methodology: We divided 30 male mice (3 months old) into three groups (n = 10); the HL group was fed a high-fat diet, the HLU group received a high-fat diet and 2 g/kg/day of grape juice, and the HLS group was fed a high-fat diet and simvastatin (20 mg/kg/day). We assessed the blood pressure profile of the mice. We also determined the levels of C-reactive protein (CRP) and lipid profile, glycemic and insulinemic profiles, and calculated the HOMA-IR. Cardiomyocyte hypertrophy, interstitial collagen deposit, and the expression of CD40 ligand (CD40L) and metalloproteinases 2 and 9 were assessed immunohistologically.

Results: After 60 days, the mice treated with grape juice showed similar results as those of the group treated with simvastatin. The use of grape fruit attenuated dyslipidemia and insulin resistance and significantly increased the levels of high cholesterol density lipoproteins (HDLc). The antioxidant potential of phenolic compounds associated with the increase in HDLc levels in the mice of the HLU group prevented the development of LVH and arterial hypertension since it inhibited the inflammatory response induced by the CD40 pathway and its ligand CD40L. Consequently, there was a lower expression of MMP-2 and MMP-9 and lower serum levels of CRP.

Conclusion: Grape juice has a hypolipidemic and cardiac protective potential, presenting a similar effect as that of simvastatin through a direct antioxidant action of phenolic compounds, or indirectly, via antioxidant action and anti-inflammatory activity of the HDLc. These results suggest that grape juice is a functional food possessing a high potential to prevent cardiovascular diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Pressure / drug effects
  • C-Reactive Protein / analysis
  • CD40 Ligand / genetics
  • CD40 Ligand / metabolism
  • Collagen / metabolism
  • Diet, High-Fat
  • Dyslipidemias / drug therapy
  • Dyslipidemias / pathology*
  • Fruit and Vegetable Juices* / analysis
  • Heart Ventricles / pathology
  • Hypertrophy, Left Ventricular / pathology
  • Hypertrophy, Left Ventricular / prevention & control*
  • Male
  • Matrix Metalloproteinase 2 / genetics
  • Matrix Metalloproteinase 2 / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Protective Agents / chemistry
  • Protective Agents / therapeutic use
  • Receptors, LDL / deficiency
  • Receptors, LDL / genetics
  • Simvastatin / therapeutic use
  • Vitis / chemistry*
  • Vitis / metabolism

Substances

  • Protective Agents
  • Receptors, LDL
  • CD40 Ligand
  • Collagen
  • C-Reactive Protein
  • Simvastatin
  • Matrix Metalloproteinase 2

Grants and funding

To CNPq and FAPEMIG for financial support, and to the Federal Institute of Education, Science and Technology of the South of Minas Gerais and to Universidade José do Rosário Vellano for support in carrying out the study. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.