Objectives: Previous studies have shown the role of oxidative stress in methanol (MeOH) neurotoxicity. In clinical practice ethanol
(EtOH) was used for the treatment of MeOH intoxication. Treatment with EtOH results in depression of the central nervous system,
which may occur even at therapeutic doses. It also induces oxidative stress. Antioxidant and neuroprotective effects of thymoquinone
(TQ) are known in different models of neurotoxicity. There are no studies investigating the protective effect of TQ against acute
MeOH intoxication. We aimed to evaluate the effect of TQ administration on serum thiobarbituric acid reactive substances (TBARS)
and Brain-Derived Neurotrophic Factor (BDNF) levels in rats with experimentally-induced MeOH intoxication.
Materials and Methods: Six groups were constituted. Methotrexate (Mtx) treatment (0.3 mg/kg/day) intraperitoneally (i.p.) was given
for 7 days to slow down the formate metabolism of all rats except controls in order to create a MeOH intoxication similar to that in
humans. On the 8th day of the experiment, 3 g/kg MeOH was injected i.p. in MeOH, EtOH and TQ groups. Four hours after MeOH
administration, 0.5 g/kg EtOH was injected i.p. in EtOH group and 30 mg/kg TQ was administered i.p. in TQ1 and TQ2 groups. In
addition, a total of 5 doses of 30 mg/kg TQ was injected i.p. 24, 48, 72 and 96 hours after the first dose in TQ2 group. Saline solution
was given i.p. in the other groups. Blood samples were obtained for evaluating serum TBARS and BDNF levels.
Results: The highest TBARS level was found in MeOH+MTx group and this increase was statistically significant as compared to
control and Mtx groups (p<0.001) . A statistically significant reduction was detected in serum TBARS levels in MeOH+Mtx+EtOH,
MeOH+Mtx+TQ1 and MeOH+Mtx+TQ2 groups (p<0.001). Maximum serum BDNF level elevation was found in MeOH+Mtx group
and this increase was statistically significant as compared to control and Mtx groups (p<0.001). Serum BDNF levels were higher in
MeOH+Mtx+EtOH, MeOH+Mtx+TQ1 and MeOH+Mtx+TQ2 groups and the difference was statistically significant (p<0.001).
Conclusions: Thymoquinone could suppress proinflammation and lipid peroxidation in MeOH intoxication, lead to rapid toxicity
adaptation, and play the role of neuroprotection more effectively than EtOH. These results may suggest that TQ could be used as an
alternative treatment option in MeOH intoxication.
Primary Language | English |
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Subjects | Clinical Sciences |
Journal Section | Original Articles |
Authors | |
Publication Date | May 30, 2022 |
Published in Issue | Year 2022 |