The Use of Chitosan-Coated Nanovesicles in Repairing Alcohol-Induced Damage of Liver Cells in Mice.
Loredana Nicoleta HilițanuLiliana Mititelu-TartauMaria BogdanBeatrice Rozalina BucaAna-Maria Raluca PăunaLiliana Lăcrămioara PavelAna Maria PelinAndreea-Daniela MecaGrațiela Eliza PopaPublished in: Medicina (Kaunas, Lithuania) (2022)
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.
Keyphrases
- alcohol consumption
- drug delivery
- oxidative stress
- wound healing
- hyaluronic acid
- high fat diet induced
- body weight
- peripheral blood
- induced apoptosis
- diabetic rats
- hydrogen peroxide
- type diabetes
- ischemia reperfusion injury
- nitric oxide
- dna damage
- newly diagnosed
- liver injury
- uric acid
- endothelial cells
- cell proliferation
- high glucose
- metabolic syndrome
- endoplasmic reticulum stress
- fatty acid
- stress induced
- case control
- water soluble