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Study of the Activity of Newly Synthesized 1,2,3-Triazole Derivatives in Various Inflammation Models

Aytmuratova Urkhiya Kallibekovna1Department of Pharmacology and Toxicology of the Institute Chemistry of Plant Substances, Academy of Sciences of the Republic of UzbekistanAzizbek Azamatov1Department of Pharmacology and Toxicology of the Institute Chemistry of Plant Substances, Academy of Sciences of the Republic of UzbekistanTursunkhodzhaeva Firuza Muratovna1Department of Pharmacology and Toxicology of the Institute Chemistry of Plant Substances, Academy of Sciences of the Republic of UzbekistanAshurmetov Rustam Isayevich1Department of Pharmacology and Toxicology of the Institute Chemistry of Plant Substances, Academy of Sciences of the Republic of UzbekistanOrtikov Ilhomjon Sobirovich2Department of Pharmacology and Chemistry, Alfraganus University, Tashkent, Uzbekistan
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Аннотация

Inflammation is a universal protective mechanism of the body that occurs in response to pathological changes caused by phlogogenic agents. The progression of the inflammatory process depends on the balance between pro-inflammatory and anti-inflammatory cytokines, primarily on the level of anti-inflammatory cytokine synthesis. The anti-inflammatory effect of triazole derivatives is based on the inhibition of the cyclooxygenase-2 enzyme, which enhances the synthesis of inflammatory mediators such as prostaglandins, bradykinin, and serotonin from arachidonic acid. In the study of the anti-inflammatory effects of 13 newly synthesized derivatives of 1,4-disubstituted 1H-1,2,3-triazole on the models of «formalin-induced paw edema», «carrageenan-induced paw edema» and «serotonin-induced aseptic arthritis» compound 5 at a dose of 100.0 mg/kg demonstrated the highest anti-inflammatory activity - 78%, 77.4%, and 79.8%, respectively. The study of the effect of this compound on the cytokine dynamics in blood serum revealed that, compared to the control group animals, it increased the level of IL-4 by 3.25 times, decreased the level of IL-6 by 5.16 times and reduced the level of TNF-α by 3.48 times.

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