CoQ10 exerts hepatoprotective effect in fructose-induced fatty liver model in rats

Pharmacol Rep. 2020 Aug;72(4):922-934. doi: 10.1007/s43440-020-00075-5. Epub 2020 Mar 10.

Abstract

Background: Excess dietary sugar is associated with deleterious metabolic effects, liver injury, and coenzyme-Q10 (CoQ10) deficiency. This study investigates the ability of CoQ10 to protect against fructose-induced hepatic damage.

Methods: Rats were fed tap water or 30% fructose for 12 weeks with or without CoQ10 (10 mg/kg, po). An additional group of rats were allowed to feed on either water or 30% fructose for 12 weeks, followed by four weeks of treatment with either the vehicle or CoQ10.

Results: Fructose-fed rats showed lower CoQ10 levels, increased systolic pressure, increased body weight, higher liquid consumption, decreased food intake and hyperglycemia. Fructose-fed rats also showed deteriorated serum and liver lipid profiles, impaired liver function tests and oxidative status, and lower expression of adiponectin receptor 1 and 2 along with higher GLUT-2 levels. Furthermore, following fructose treatment, tyrosine kinase-PI3K pathway was inhibited. Additionally, there was an increase in the levels of apoptotic markers and serum visfatin and a decrease in the levels of adiponectin and soluble receptor of the advanced glycated end product. Consequently, several histopathological changes were detected in the liver. Concurrent or three months post-exposure administration of CoQ10 in fructose rats significantly reversed or attenuated all the measured parameters and hepato-cytoarchitecture alterations.

Conclusion: This study suggests CoQ10 supplement as a possible prophylaxis or treatment candidate for fructose-induced liver injury.

Keywords: Adiponectin; Lipid profile; PI3K; Tyrosine kinase.

MeSH terms

  • Animals
  • Fatty Liver / chemically induced
  • Fatty Liver / metabolism*
  • Fatty Liver / prevention & control*
  • Fructose / toxicity*
  • Liver / drug effects
  • Liver / enzymology*
  • Male
  • Oxidative Stress / drug effects
  • Oxidative Stress / physiology
  • Protective Agents / administration & dosage
  • Rats
  • Rats, Wistar
  • Ubiquinone / administration & dosage
  • Ubiquinone / analogs & derivatives*
  • Ubiquinone / metabolism

Substances

  • Protective Agents
  • Ubiquinone
  • Fructose
  • coenzyme Q10