The Use of Chitosan-Coated Nanovesicles in Repairing Alcohol-Induced Damage of Liver Cells in Mice

Medicina (Kaunas). 2022 Jun 5;58(6):762. doi: 10.3390/medicina58060762.

Abstract

Background and Objectives In the past few decades, the studies concerning the natural polysaccharide chitosan have been centered on a new direction: its hepatoprotective action. The aim of our study was to evaluate the influence of previously designed chitosan lipid vesicles on the liver damage induced by alcohol consumption in mice. Materials and Methods The study involved the oral administration of substances in one daily dose as follows: Group 1 (control): water; Group 2 (control alcohol): 5% alcohol in water; Group 3 (CHIT): 0.1 mL/10 g body weight chitosan solution in animals treated with alcohol; Group 4 (CHIT-ves): 0.1 mL/10 g body chitosan vesicles in animals treated with alcohol; Group 5 (AcA): 200 mg/kg body ascorbic acid in animals treated with alcohol. In order to evaluate liver damage after alcohol consumption, the following hematological parameters were tested: the activity of alanine aminotransferase, aspartate aminotransferase and lactate dehydrogenase; serum values of urea and creatinine; the phagocytic capacity of polymorphonuclear neutrophilsin peripheral blood;serum opsonic capacity;bactericidal capacity of peritoneal macrophages; and the activity of malondialdehyde, glutathione peroxidase, superoxide dismutase and lactate dehydrogenase. Results and Conclusions The treatment with chitosan vesicles decreased liver enzyme activity and reduced the oxidative stress disturbances in alcoholic mice, thus repairing the hepatic functional and structural damages. These beneficial activities of chitosan vesicles were comparable with ascorbic acid effects in alcoholic mice.

Keywords: alcohol; chitosan; hepatoprotective; lipid vesicles; mice.

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Ascorbic Acid / pharmacology
  • Chitosan* / pharmacology
  • Chitosan* / therapeutic use
  • Ethanol / pharmacology
  • Lactate Dehydrogenases / metabolism
  • Liver
  • Mice
  • Oxidative Stress
  • Water / metabolism
  • Water / pharmacology

Substances

  • Antioxidants
  • Water
  • Ethanol
  • Chitosan
  • Lactate Dehydrogenases
  • Ascorbic Acid

Grants and funding

This work is part of Loredana Nicoleta Hilitanu’s PhD studies and was financially supported by The Doctoral School of “Grigore T. Popa” University of Medicine and Pharmacy, Iasi, Romania (Doctoral Grant financing approval 20.01.2021).