Jorm C M, Stamford J A
Anaesthetics Unit, London Hospital Medical College, Royal London Hospital, Whitechapel.
Br J Anaesth. 1993 Sep;71(3):447-9. doi: 10.1093/bja/71.3.447.
We have examined the effects of the highly selective alpha 2-adrenoceptor agonist, dexmedetomidine, on noradrenaline release and cell firing in isolated, superfused slices of rat locus coeruleus. Dexmedetomidine decreased both noradrenaline release and cell firing rate in a concentration-dependent fashion, with an EC50 of 3.97 (SEM 0.97) x 10(-9) mol litre-1 for noradrenaline release and 0.92 (0.53) x 10(-9) mol litre-1 for unit activity. Both effects were reversed completely by the selective alpha 2 antagonist, atipamezole 10(-6) mol litre-1. These results suggest that cell firing and noradrenaline release are under alpha 2 receptor control and that dexmedetomidine potently stimulates these receptors. We conclude that these effects are consistent with the locus coeruleus being a major site of action of the hypnotic anaesthetic alpha 2 agonists.
我们研究了高选择性α2-肾上腺素能受体激动剂右美托咪定对大鼠蓝斑离体灌流切片中去甲肾上腺素释放和细胞放电的影响。右美托咪定以浓度依赖性方式降低去甲肾上腺素释放和细胞放电率,去甲肾上腺素释放的EC50为3.97(标准误0.97)×10−9mol/L,单位活动的EC50为0.92(0.53)×10−9mol/L。这两种作用均被选择性α2拮抗剂阿替美唑10−6mol/L完全逆转。这些结果表明,细胞放电和去甲肾上腺素释放受α2受体控制,且右美托咪定能有效刺激这些受体。我们得出结论,这些作用与蓝斑是催眠麻醉性α2激动剂的主要作用部位一致。