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IEM-1460 and Spermine Potentiate the Analgesic Actions of Fentanyl and Analgin in Rats

机译:IEM-1460和精胺增强芬太尼和安乃近在大鼠中的镇痛作用

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Intramuscular administration of the minimum effective doses (MED) of the central analgesics fentanyl and Analgin [translator's note: metamizole], the NMDA receptor polyamine site agonist spermine, and IEM- 1460, an AMPA receptor blocker and agonist of the NMDA receptor polyamine site, induced maximal analgesic effects in the tailfl ick test in rats. Combined intramuscular administration of Analgin and IEM-1460 and spermine at threshold doses inactive when given alone (1/5 MED) allowed the MED of Analgin to be reduced by a factor of 120 when given in combination with IEM-1460 and by a factor of 10 when given in combination with spermine. Combined intramuscular administration of fentanyl with IEM-1460 and spermine at these threshold doses decreased the MED of fentanyl by a factor of 150 when used with IEM-1460 and a factor of 15 when used with spermine.
机译:肌内注射中央镇痛药芬太尼和Analgin的最小有效剂量(MED)[译者注:metamizole],NMDA受体多胺位点激动剂精胺和IEM-1460,AMPA受体阻滞剂和NMDA受体多胺位点激动剂,在大鼠的甩尾试验中具有最大的镇痛作用。单独肌注Analgin和IEM-1460和精胺的肌肉联合给药(单独给药时无效)(1/5 MED)可使与IEM-1460联合给药时Analgin的MED降低120倍,与精胺结合使用时为10。在这些阈值剂量下联合肌内注射芬太尼与IEM-1460和精胺,与IEM-1460一起使用时芬太尼的MED降低150倍,与精胺一起时降低15倍。

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