HEPATOPROTECTIVE ACTIVITY OF EXOGENOUS RNA

Ukr Biochem J. 2015 Jul-Aug;87(4):37-44. doi: 10.15407/ubj87.04.037.

Abstract

Hepatoprotective activity of Nuclex, a pharmaceutical composed of low-molecular yeast RNA, was investigated during acute and chronic thioacetamide-induced hepatotoxicity. It is demonstrated, that Nuclex administration at a dose of 200 mg/kg during acute and chronic liver injury produces hepatoprotective effect, which is associated with decrease in liver parenchyma lesions and in its inflammatory infiltration. Nuclex application attenuates thioacetamide-induced free radical damage of hepatic biopolymers, expressed in the reduction of TBA-reactive products, carbonyl derivatives, and recovery of protein thiol groups and reduced glutathione levels.

MeSH terms

  • Administration, Oral
  • Animals
  • Chemical and Drug Induced Liver Injury / drug therapy*
  • Chemical and Drug Induced Liver Injury / metabolism
  • Chemical and Drug Induced Liver Injury / pathology
  • Chemical and Drug Induced Liver Injury, Chronic / drug therapy*
  • Chemical and Drug Induced Liver Injury, Chronic / metabolism
  • Chemical and Drug Induced Liver Injury, Chronic / pathology
  • Dipeptides / pharmacology
  • Free Radicals / antagonists & inhibitors
  • Free Radicals / metabolism
  • Glutathione / metabolism
  • Injections, Intraperitoneal
  • Liver / drug effects*
  • Liver / metabolism
  • Liver / pathology
  • Mice
  • Mice, Inbred C57BL
  • Molecular Weight
  • Neutrophil Infiltration / drug effects
  • Protective Agents / pharmacology*
  • RNA, Fungal / pharmacology*
  • Sulfhydryl Compounds / metabolism
  • Thioacetamide
  • Thiobarbiturates / chemistry

Substances

  • Dipeptides
  • Free Radicals
  • Protective Agents
  • RNA, Fungal
  • Sulfhydryl Compounds
  • Thiobarbiturates
  • Thioacetamide
  • Glutathione
  • thiobarbituric acid
  • arginine glutamate