Willdeck-Lund G, Nilsson B A
Acta Anaesthesiol Scand. 1979 Feb;23(1):78-88. doi: 10.1111/j.1399-6576.1979.tb01424.x.
Four local anaesthetic agents, lidocaine, prilocaine, bupivacaine and etidocaine with and without adrenaline, were tested regarding their influence on the contraction amplitude, tone and frequency of contractions of human myometrium in vitro. All four drugs had a dose-related inhibitory effect on the amplitude. This was enhanced by adrenaline. The two short-acting and the two long-acting agents were tested in equianalgesic doses in a crossover test. Lidocaine and etidocaine had a significantly greater inhibitory effect on the spontaneous myometrial contractions than prilocaine and bupivacaine. With all drugs, except etidocaine, the tone increased with increasing drug concentrations in the bath. The changes in frequency were inconsistent. Based on the concentrations required to produce 50% inhibition, lidocaine, bupivacaine and etidocaine were, respectively, 1.3, 6.5 and 8.3 times more potent than prilocaine; the corresponding figures for the anaesthetic effect on isolated nerves are reported to be 1.5, 5.3, and 5.3. The inhibitory effect of etidocaine declined with time, in contrast to the other local anaesthetic agents tested.
对四种局部麻醉剂,即利多卡因、丙胺卡因、布比卡因和依替卡因,分别在添加和不添加肾上腺素的情况下,测试了它们对体外人子宫肌层收缩幅度、张力和收缩频率的影响。所有四种药物对幅度均有剂量相关的抑制作用。肾上腺素可增强这种作用。在交叉试验中,以等效镇痛剂量对两种短效和两种长效药物进行了测试。利多卡因和依替卡因对子宫肌层自发性收缩的抑制作用明显大于丙胺卡因和布比卡因。除依替卡因外,所有药物均使浴槽中药物浓度增加时张力升高。频率变化不一致。根据产生50%抑制所需的浓度,利多卡因、布比卡因和依替卡因的效力分别比丙胺卡因高1.3倍、6.5倍和8.3倍;据报道,它们对离体神经的麻醉作用的相应倍数分别为1.5、5.3和5.3。与其他测试的局部麻醉剂不同,依替卡因的抑制作用随时间下降。