Protective effect of dietary flavonoid quercetin against lipemic-oxidative hepatic injury in hypercholesterolemic rats

Pharm Biol. 2012 Aug;50(8):1019-25. doi: 10.3109/13880209.2012.655424.

Abstract

Context: Quercetin, a dietary-derived flavonoid, is ubiquitous in fruits and vegetables and plays important roles in human health by virtue of its antioxidant activity.

Objective: This study was conducted to investigate the possible modulatory effect of quercetin against hepatic lipemic-oxidative injury in rats fed with a high cholesterol diet (HCD), and to highlight the underlying mechanisms of such effect.

Materials and methods: Different groups of male Sprague-Dawley rats were used; one group was treated by gavage with HCD cocktail (1 mL/100 g) whereas another group was orally administered HCD-enriched with quercetin (15 mg/kg). Corresponding control animals were also used.

Results: Quercetin administration significantly decreased liver triglycerides (24%), liver total cholesterol (TC) (22%), serum TC (20%), serum low-density lipoprotein cholesterol (31%), and duplicated serum high-density lipoprotein cholesterol (HDL-C). This study also revealed that quercetin administration significantly reduced the activity of serum alanine aminotransferase (41%), aspartate aminotransferase (51%), and γ-glutamyl transpeptidase (G-GT) (35%). Significant inhibition of thiobarbituric acid-reacting substances (40%), together with a valuable enhancement of reduced glutathione (GSH) content (53%) in the liver homogenates, was observed. In addition, quercetin-treated hypercholesterolemic animals exhibited a reasonable improvement of hepatic antioxidant enzymes. Moreover, serum and liver content of nitric oxide (NO) were markedly decreased in this model (26 and 25%, respectively), and were almost normalized following quercetin administration.

Discussion and conclusion: These data revealed that quercetin has the ability to ameliorate HCD-induced lipemic-oxidative injury in rat liver possibly through its antioxidant potential and/or increased NO bioavailability.

MeSH terms

  • Animals
  • Anticholesteremic Agents / therapeutic use*
  • Antioxidants / therapeutic use*
  • Cholesterol / blood
  • Cholesterol / metabolism
  • Cholesterol, Dietary / adverse effects
  • Cholesterol, HDL / blood
  • Cholesterol, LDL / blood
  • Dietary Supplements*
  • Glutathione / metabolism
  • Hypercholesterolemia / blood
  • Hypercholesterolemia / metabolism
  • Hypercholesterolemia / prevention & control*
  • Lipid Peroxides / metabolism
  • Liver / metabolism*
  • Male
  • Nitric Oxide / blood
  • Nitric Oxide / metabolism
  • Oxidation-Reduction
  • Oxidative Stress*
  • Quercetin / therapeutic use*
  • Rats
  • Rats, Sprague-Dawley
  • Triglycerides / metabolism

Substances

  • Anticholesteremic Agents
  • Antioxidants
  • Cholesterol, Dietary
  • Cholesterol, HDL
  • Cholesterol, LDL
  • Lipid Peroxides
  • Triglycerides
  • Nitric Oxide
  • Cholesterol
  • Quercetin
  • Glutathione