Effects of hydroxytyrosol on cardiovascular biomarkers in experimental diabetes mellitus

J Nutr Biochem. 2016 Nov:37:94-100. doi: 10.1016/j.jnutbio.2016.07.015. Epub 2016 Aug 26.

Abstract

The aim of this study was to assess the influence of hydroxytyrosol (HT) on cardiovascular biomarkers and morphometric parameters of the arterial wall in streptozotocin-diabetic rats. Seven groups of rats (N=10 per group) were studied for 2 months: nondiabetic rats (NDR), diabetic rats treated with saline (DR) and DR treated with HT (0.5, 1, 2.5, 5 and 10 mg kg-1 day-1 p.o.). DR had higher platelet aggregation values, higher thromboxane B2, plasma lipid peroxidation, 3-nitrotyrosine, oxidized LDL (oxLDL), myeloperoxidase, vascular cell adhesion molecule 1 (VCAM-1) and interleukin-1β (IL-1β) concentrations, and lower aortic 6-keto-prostaglandin F and nitric oxide production than NDR. Aortic wall area and smooth muscle cell count were also higher in DR than in NDR. HT significantly reduced both oxidative and nitrosative stress, oxLDL concentration, VCAM-1 and inflammatory mediators, platelet aggregation and thromboxane B2 production. Morphometric values in the aortic wall were reduced to values near those in NDR. In conclusion, HT influenced the major biochemical processes leading to diabetic vasculopathy, and reduced cell proliferation in the vascular wall in this experimental model.

Keywords: Diabetes; Hydroxytyrosol; Inflammatory mediators; Oxidative stress; Platelets; Vasculopathy.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / administration & dosage
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
  • Antioxidants / administration & dosage
  • Antioxidants / therapeutic use*
  • Aorta, Abdominal
  • Biomarkers / blood
  • Biomarkers / metabolism
  • Cardiovascular Diseases / complications
  • Cardiovascular Diseases / immunology
  • Cardiovascular Diseases / prevention & control*
  • Diabetes Mellitus, Experimental / complications
  • Diabetes Mellitus, Experimental / diet therapy*
  • Diabetes Mellitus, Experimental / metabolism
  • Diabetes Mellitus, Experimental / pathology
  • Diabetic Angiopathies / immunology
  • Diabetic Angiopathies / prevention & control*
  • Diabetic Cardiomyopathies / immunology
  • Diabetic Cardiomyopathies / prevention & control*
  • Dietary Supplements*
  • Endothelium, Vascular / immunology
  • Endothelium, Vascular / metabolism
  • Endothelium, Vascular / pathology
  • Inflammation Mediators / antagonists & inhibitors
  • Inflammation Mediators / blood
  • Inflammation Mediators / metabolism
  • Lipid Peroxidation
  • Lipoproteins, LDL / blood
  • Male
  • Muscle, Smooth, Vascular / immunology
  • Muscle, Smooth, Vascular / metabolism
  • Muscle, Smooth, Vascular / pathology
  • Oxidative Stress
  • Phenylethyl Alcohol / administration & dosage
  • Phenylethyl Alcohol / analogs & derivatives*
  • Phenylethyl Alcohol / therapeutic use
  • Platelet Aggregation
  • Rats, Wistar
  • Reactive Nitrogen Species / antagonists & inhibitors
  • Reactive Nitrogen Species / blood
  • Reactive Nitrogen Species / metabolism
  • Streptozocin

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Antioxidants
  • Biomarkers
  • Inflammation Mediators
  • Lipoproteins, LDL
  • Reactive Nitrogen Species
  • oxidized low density lipoprotein
  • 3,4-dihydroxyphenylethanol
  • Streptozocin
  • Phenylethyl Alcohol