EFFECT OF RESVERATROL ON CYTOLYTIC PROCESSES IN RATS POISONING WITH SODIUM BENZOATE

Authors

  • N. R. Nechai IVAN HORBACHEVSKY TERNOPIL NATIONAL MEDICAL UNIVERSITY OF THE MINISTRY OF HEALTH OF UKRAINE
  • L. S. Fira IVAN HORBACHEVSKY TERNOPIL NATIONAL MEDICAL UNIVERSITY OF THE MINISTRY OF HEALTH OF UKRAINE

DOI:

https://doi.org/10.11603/mcch.2410-681X.2026.i3.16796

Keywords:

sodium benzoate; resveratrol; cytolytic processes; organ-specific enzymes; white rats

Abstract

Introduction. Today, the food industry widely uses a range of chemical additives, among which one of the most common preservatives is E211 – sodium benzoate (sodium salt of benzoic acid). The permissible daily intake for humans is < 5 mg/kg of body weight. When the permissible intake is exceeded, sodium benzoate has a toxic effect on the liver and kidneys, and provokes exacerbation of asthma symptoms. The aim of the study. To study the influence of resveratrol on the permeability of cell membranes after poisoning rats with sodium benzoate. Research Methods. The study was conducted on 42 white sexually mature non-linear male rats in compliance with all the rules of the European Convention for the Protection of Vertebrate Animals. The experimental rats were divided into 3 groups. The first group consisted of intact rats, the rats of the second group received daily sodium benzoate at a dose of 30 mg/kg of body weight. The third group of rats, on the background of sodium benzoate poisoning, was intragastrically injected with resverazine (active ingredient resveratrol) at a dose of 20 mg/kg of body weight. The animals were euthanized under thiopental anesthesia (60 mg/kg). The rats were removed from the experiment 14, 21 and 28 days after the start of the administration of sodium benzoate and resveratrol. Cytolytic processes in rats were assessed by the activity of alanine and aspartate aminotransferase, gammaglutamyl transpeptidase, and erythrocyte intoxication index. Statistical processing of the results was carried out using the STATISTICA 13 program. The significance of the difference between independent quantitative values was determined by the Mann–Whitney test. Results and Discussion. Poisoning of rats with sodium benzoate at a dose of 30 mg/kg of body weight led to a progressive increase in the activity of ALT, AST and GGTP in the blood serum throughout the experiment. The highest activity was recorded 28 days after the start of poisoning (ALT by 1.6 times, AST and GGTP by 2.4 times exceeded this indicator in intact rats). The use of resveratrol led to a decrease in the activity of these enzymes in the blood serum. In the liver of rats, a decrease in the activity of ALT, AST and GGTP was noted after poisoning with sodium benzoate. Resveratrol showed an effective effect on these indicators, increasing them in the liver, almost to the normal level. Under the influence of sodium benzoate, the permeability of erythrocyte membranes increased (by 47 % at the end of the experiment). A positive effect of resveratrol on this indicator was noted; after its application, EII gradually decreased and 28 days after the start of BN poisoning, it was 2 times lower than that in poisoned rats. Conclusions. The results of the study showed that poisoning of rats with sodium benzoate at a dose of 30 mg/kg led to changes in the permeability of the plasma membranes of hepatocytes and erythrocytes. A positive effect of resveratrol on the permeability of cytoplasmic membranes in rats poisoned with sodium benzoate was noted, as indicated by the normalization of the activity of organ-specific enzymes in both the blood serum and the liver of experimental animals, as well as a decrease in the permeability of the erythrocyte membrane. The data obtained are the basis for further studies of this antioxidant under the conditions of poisoning of rats with various toxicants.

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Published

2026-09-30

Issue

Section

ORIGINAL INVESTIGATIONS

How to Cite

EFFECT OF RESVERATROL ON CYTOLYTIC PROCESSES IN RATS POISONING WITH SODIUM BENZOATE. (2026). Medical and Clinical Chemistry, 3, 65-72. https://doi.org/10.11603/mcch.2410-681X.2026.i3.16796