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Long-Lasting Anti-Inflammatory and Antinociceptive Effects of Acute Ammonium Glycyrrhizinate Administration: Pharmacological Biochemical and Docking Studies

机译:急性甘草酸铵铵的持久抗炎和镇痛作用:药理生化和对接研究

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摘要

The object of the study was to estimate the long-lasting effects induced by ammonium glycyrrhizinate (AG) after a single administration in mice using animal models of pain and inflammation together with biochemical and docking studies. A single intraperitoneal injection of AG was able to produce anti-inflammatory effects in zymosan-induced paw edema and peritonitis. Moreover, in several animal models of pain, such as the writhing test, the formalin test, and hyperalgesia induced by zymosan, AG administered 24 h before the tests was able to induce a strong antinociceptive effect. Molecular docking studies revealed that AG possesses higher affinity for microsomal prostaglandin E synthase type-2 compared to type-1, whereas it seems to locate better in the binding pocket of cyclooxygenase (COX)-2 compared to COX-1. These results demonstrated that AG induced anti-inflammatory and antinociceptive effects until 24–48 h after a single administration thanks to its ability to bind the COX/mPGEs pathway. Taken together, all these findings highlight the potential use of AG for clinical treatment of pain and/or inflammatory-related diseases.
机译:该研究的目的是使用疼痛和炎症的动物模型以及生化和对接研究,评估在小鼠中单次施用甘草酸铵(AG)诱导的持久作用。一次腹膜内注射AG能够在酵母聚糖诱导的爪水肿和腹膜炎中产生抗炎作用。此外,在几种动物疼痛模型中,如扭体试验,福尔马林试验和由酵母聚糖诱导的痛觉过敏,试验前24小时施用AG能够诱导强烈的镇痛作用。分子对接研究表明,与1型相比,AG对2型微粒体前列腺素E合酶具有更高的亲和力,而与COX-1相比,它似乎在环氧合酶(COX)-2的结合口袋中定位更好。这些结果表明,由于AG具有结合COX / mPGEs途径的能力,因此在单次给药后直至24-48 h都具有抗炎和镇痛作用。综上所述,所有这些发现强调了AG在疼痛和/或炎症相关疾病的临床治疗中的潜在用途。

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