Effect of Cyclooxygenase Inhibitors Etoricoxib and Diclofenac Sodium and Their Combinations with Mexidol on Behavior in Rats
Ivanova Ea, A. I. Matyushkin, Анастасия Геннадьевна Васильчук, Татьяна Александровна Воронина
Abstract
Ivanova Ea, A. I. Matyushkin, Анастасия Геннадьевна Васильчук, Татьяна Александровна Воронина
Abstract
Abstract The effect of nonsteroidal anti-inflammatory drugs (NSAIDs), selective cyclooxygenase (COX)-2 inhibitor etoricoxib and nonselective COX inhibitor diclofenac sodium, on the behavior of rats was evaluated with a single oral administration at doses of 1 and 10 mg/kg individually and in combination with 2-ethyl-6-methyl-3-hydroxypyridine succinate (mexidol). Both COX inhibitors at a dose of 10 mg/kg decrease locomotor activity in the open field test, and the selective COX-2 inhibitor at a dose of 10 mg/kg also increases the duration of immobility of animals in the tail suspension test. The use of etoricoxib and diclofenac sodium at a low dose (1 mg/kg) with mexidol at a dose of 25 mg/kg, in which the latter enhances the anti-inflammatory effect of the COX inhibitors, does not lead to behavioral deviations similar to those associated with the NSAIDs at a dose of 10 mg/kg. Moreover, combinations of COX inhibitors (1 mg/kg) and mexidol (25 mg/kg) increase the locomotor activity of rats. This justifies further research into the effect of antioxidants on the severity of the main and side effects of NSAIDs, especially when administered as a course.
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Abstract The effect of nonsteroidal anti-inflammatory drugs (NSAIDs), selective cyclooxygenase (COX)-2 inhibitor etoricoxib and nonselective COX inhibitor diclofenac sodium, on the behavior of rats was evaluated with a single oral administration at doses of 1 and 10 mg/kg individually and in combination with 2-ethyl-6-methyl-3-hydroxypyridine succinate (mexidol). Both COX inhibitors at a dose of 10 mg/kg decrease locomotor activity in the open field test, and the selective COX-2 inhibitor at a dose of 10 mg/kg also increases the duration of immobility of animals in the tail suspension test. The use of etoricoxib and diclofenac sodium at a low dose (1 mg/kg) with mexidol at a dose of 25 mg/kg, in which the latter enhances the anti-inflammatory effect of the COX inhibitors, does not lead to behavioral deviations similar to those associated with the NSAIDs at a dose of 10 mg/kg. Moreover, combinations of COX inhibitors (1 mg/kg) and mexidol (25 mg/kg) increase the locomotor activity of rats. This justifies further research into the effect of antioxidants on the severity of the main and side effects of NSAIDs, especially when administered as a course.
Key concepts: Etoricoxib, Diclofenac Sodium, Cyclooxygenase, Diclofenac, Chemistry, Pharmacology, Medicine, Biochemistry