Sato K, Windisch K, Matko I, Vizi E S
Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary.
Br J Anaesth. 1999 Jun;82(6):904-9. doi: 10.1093/bja/82.6.904.
We have studied the effect of non-depolarizing neuromuscular blocking agents, at concentrations present in serum during anaesthesia, on release of [3H]-norepinephrine ([3H]NE) from superfused atrial appendage obtained during cardiac surgery from 48 patients. Three of the neuromuscular blocking agents (pancuronium, gallamine and rocuronium), which are known to cause an increase in heart rate during anaesthesia, increased stimulation-evoked release of [3H]NE. In contrast, (+)tubocurarine and pipecuronium, neuromuscular blocking agents that do not cause tachycardia, did not affect release of NE. Org 9487 significantly enhanced release while SZ1677 was ineffective, even at concentrations higher than those expected after administration of a 2 x ED95 dose. Atropine enhanced release. These data suggest that the axon terminals of sympathetic nerves in human heart have muscarinic heteroreceptors whose activation by acetylcholine (ACh) released from the vagal nerve reduces release of NE. This action contributes to lowering of heart rate. Therefore, any neuromuscular blocking agent with antimuscarinic actions and capable of increasing the release of NE may produce tachycardia.
我们研究了麻醉期间血清中存在的非去极化神经肌肉阻滞剂浓度对48例心脏手术患者获取的体外灌流心耳释放[3H]-去甲肾上腺素([3H]NE)的影响。三种已知在麻醉期间会导致心率增加的神经肌肉阻滞剂(泮库溴铵、加拉明和罗库溴铵)增加了刺激诱发的[3H]NE释放。相比之下,不会引起心动过速的神经肌肉阻滞剂(+)筒箭毒碱和哌库溴铵对NE的释放没有影响。Org 9487显著增强了释放,而SZ1677即使在高于给予2倍ED95剂量后预期的浓度下也无效。阿托品增强了释放。这些数据表明,人心脏交感神经的轴突末梢具有毒蕈碱异受体,迷走神经释放的乙酰胆碱(ACh)激活这些受体可减少NE的释放。这一作用有助于降低心率。因此,任何具有抗毒蕈碱作用且能够增加NE释放的神经肌肉阻滞剂都可能导致心动过速。