Wali F A, Suer A H, Greenidge E, Tugwell A C, Hayter A
Gen Pharmacol. 1987;18(4):351-5. doi: 10.1016/0306-3623(87)90090-5.
The effects of 5 different local anaesthetics, lignocaine, prilocaine, etidocaine, mepivacaine, bupivacaine, on uptake of Ca2+, Na+ and K+ were studied, using a Kone Microlyte Analyzer, into 3 different types of muscle fibres, the rat ileum, rat diaphragm and human isolated saphenous vein. The aim of the present experiments was to see if local anaesthetics had a calcium antagonistic activity, like that produced by calcium antagonists, e.g. verapamil. The results showed that local anaesthetics in moderate and high concentrations (more than 100 microM) depressed uptake of Ca2+, as well as the Na+ and K+, although the depression of the uptake of Ca2+ was 7 and 2 times less than those of Na+ and K+. In low concentrations (1-10 microM), the local anaesthetics had no or little effect on Ca2+ uptake, although they still significantly reduced Na+ and K+ uptake. It was concluded that the effect of local anaesthetics on uptake of Ca2+, Na+ and K+ into rat ileum, diaphragm and human saphenous vein, is concentration-dependent, and that only at high concentrations do they have a calcium antagonistic activity in muscle. Furthermore, there was no clear evidence that the effect of local anaesthetics was species-dependent, since the uptake of Ca2+ was depressed by only about 17% more in smooth muscle than in skeletal muscle.
使用Kone微量电解质分析仪,研究了5种不同的局部麻醉药,即利多卡因、丙胺卡因、依替卡因、甲哌卡因、布比卡因,对3种不同类型肌纤维(大鼠回肠、大鼠膈肌和人离体隐静脉)摄取Ca2+、Na+和K+的影响。本实验的目的是观察局部麻醉药是否具有钙拮抗活性,类似于钙拮抗剂(如维拉帕米)所产生的活性。结果表明,中等浓度和高浓度(超过100微摩尔)的局部麻醉药会抑制Ca2+以及Na+和K+的摄取,尽管Ca2+摄取的抑制程度比Na+和K+摄取的抑制程度分别低7倍和2倍。在低浓度(1 - 10微摩尔)时,局部麻醉药对Ca2+摄取没有或几乎没有影响,尽管它们仍然显著降低了Na+和K+的摄取。得出的结论是,局部麻醉药对大鼠回肠、膈肌和人隐静脉摄取Ca2+、Na+和K+的影响是浓度依赖性的,并且只有在高浓度时它们在肌肉中才具有钙拮抗活性。此外,没有明确的证据表明局部麻醉药的作用具有种属依赖性,因为平滑肌中Ca2+摄取的抑制程度仅比骨骼肌中高约17%。