Study of Correction of Somatic Pain under the Conditions of Experimental Pathology of Multiple Sclerosis

The purpose of the study was to experimentally substantiate the ways of pharmacological correction of somatic pain syndrome in conditions of the experimental equivalent of multiple sclerosis through a comparative system analysis and the use of complex methodological approaches. Materials and methods...

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Veröffentlicht in:Ukraïnsʹkij žurnal medicini, bìologìï ta sportu bìologìï ta sportu, 2021-12, Vol.6 (6), p.66-73
Hauptverfasser: Nefodov, O. O., Myasoed, Yu. P., Solomenko, M. V., Velikorodna-Tanasiychuk, O. V., Baklunov, V. V., Adegova, L. Ya, Chirkin, V. I., Malchugin, R. K.
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Sprache:eng
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Zusammenfassung:The purpose of the study was to experimentally substantiate the ways of pharmacological correction of somatic pain syndrome in conditions of the experimental equivalent of multiple sclerosis through a comparative system analysis and the use of complex methodological approaches. Materials and methods. To study multiple sclerosis, we used an experimental model with autoimmune mechanisms of inflammatory demyelination – a model of experimental allergic encephalomyelitis. To assess the antinociceptive activity of painkillers, we used the method of electrical stimulation of the rats’ tail root. The activity of the enzyme prostaglandin H-synthetase was also determined. Results and discussion. A comparative analysis of the analgesic activity indicators of combinations of methylprednisolone with analgesics under the condition of the formed experimental allergic encephalomyelitis showed that their antinociceptive potential (taking into account the basic therapy with methylprednisolone) decreased in the series meloxicam > lornoxicam ≈ ketorolac ≈ paracetamol > celecofenacoxib ≈ sodium diclofupene ≈ diclofupene ≈ diclofupene. Accordingly, the maximum effect on the threshold of nociception under these experimental conditions was exerted by meloxicam and lornoxicam. The combined administration of methylprednisolone with diclofenac sodium, celecoxib and meloxicam reduced the activity of prostaglandin N-synthetase in the brain structures by 49.8% (p
ISSN:2415-3060
2522-4972
DOI:10.26693/jmbs06.06.066