Quercetin decreases the activity of matrix metalloproteinase-2 and ameliorates vascular remodeling in renovascular hypertension

Atherosclerosis. 2018 Mar:270:146-153. doi: 10.1016/j.atherosclerosis.2018.01.031. Epub 2018 Jan 31.

Abstract

Background and aims: Increased activity of matrix metalloproteinase (MMP)-2 is observed in aortas of different models of hypertension, and its activation is directly mediated by oxidative stress. As quercetin is an important flavonoid with significant antioxidant effects, the hypothesis here is that quercetin will reduce increased MMP-2 activity by decreasing oxidative stress in aortas of hypertensive rats and then ameliorate hypertension-induced vascular remodeling.

Methods: Male two-kidney one-clip (2K1C) hypertensive Wistar rats and controls were treated with quercetin (10 mg/kg/day) or its vehicle for three weeks by gavage. Rats were then analyzed at five weeks of hypertension. Systolic blood pressure (SBP) was determined by tail-cuff plethysmography. Aortas were used to determine MMP activity by in situ zymography and reactive oxygen species (ROS) levels by dihydroethidium. Western blot was performed to detect focal adhesion kinase (FAK) and phosphorylated-FAK levels.

Results: SBP was increased in 2K1C rats and only a borderline reduction in SBP was observed after treating 2K1C rats with quercetin. Cross-sectional area and the number of vascular smooth muscle cells were significantly increased in aortas of hypertensive rats, and quercetin reduced them. Quercetin reduced ROS levels in aortas of 2K1C rats and the increased activity of gelatinases in situ. However, quercetin did not affect the levels of tissue inhibitor of MMP (TIMP)-2 and did not interfere with FAK and p-FAK levels in aortas of hypertensive rats. Furthermore, different concentrations of quercetin did not directly reduce the activity of human recombinant MMP-2 in vitro.

Conclusions: Quercetin reduces hypertension-induced vascular remodeling, oxidative stress and MMP-2 activity in aortas.

Keywords: Antioxidant; Hypertension; Matrix metalloproteinase; Oxidative stress; Vascular remodeling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / pharmacology*
  • Aorta / drug effects*
  • Aorta / enzymology
  • Aorta / pathology
  • Aorta / physiopathology
  • Disease Models, Animal
  • Focal Adhesion Kinase 1 / metabolism
  • Hypertension, Renovascular / drug therapy*
  • Hypertension, Renovascular / enzymology
  • Hypertension, Renovascular / pathology
  • Hypertension, Renovascular / physiopathology
  • Male
  • Matrix Metalloproteinase 2 / metabolism*
  • Oxidative Stress / drug effects*
  • Phosphorylation
  • Quercetin / pharmacology*
  • Rats, Wistar
  • Reactive Oxygen Species / metabolism
  • Signal Transduction / drug effects
  • Vascular Remodeling / drug effects*

Substances

  • Antioxidants
  • Reactive Oxygen Species
  • Quercetin
  • Focal Adhesion Kinase 1
  • Ptk2 protein, rat
  • Matrix Metalloproteinase 2
  • Mmp2 protein, rat