Authors
Malygin A. S.
Resident Physician, Chair for Pharmacology and Clinical Pharmacology1
1 - Tver State Medical University, Tver, Russia
Corresponding author
Malygin A.S.; E-mail: dr.a.s.m@yandex.ru
Conflict of interests
None declared.
Funding
The study had no sponsorship.
Abstract
Aim: Experimental evaluation of the acute toxicity and neurotoxicity of a new amide derivative of valproic acid and 1,3,4-thiadiazole. Materials and Methods: The acute toxicity of N-(5-ethyl-1,3,4-thiadiazol-2-yl)-2-propylpentanamide (valprazolamide) was evaluated by probit analysis in experiments in mice. Neurotoxicity was determined in a rotating rod test and pull-up bar test in mice. The effect of valprazolamide on the exploratory behavior of mice in «open field» test and in a «dark/light transition» test was evaluated. Results: The DL 50 and TD50 values of valprazolamide (intraperitoneally) for mice were 924.8 (756.9-1063.7) mg/kg and 456.7 (325.4–603.6) mg/kg, respectively. Conclusion: A new amide derivative of valproic acid and 1,3,4-thiadiazole (valprazolamide) belongs to the group of low-toxic substances.
Key words
antiepileptic drugs, valproic acid, 1,3,4-thiadiazole, acute toxicity, neurotoxicity
DOI
References
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