Török J, Sartoris M, Bauer V
Drugs Exp Clin Res. 1986;12(9-10):799-807.
The effect of carbamate local anaesthetics (pentacaine and heptacaine) on contractile responses induced by transmural nerve stimulation, exogenous noradrenaline (NA) and KCl, as well as on noradrenaline-induced Ca2+ mobilization, were investigated in isolated rabbit blood vessels under isometric conditions. Pentacaine and heptacaine inhibited the neurogenic contractions and those elicited by exogenous NA and KCl. The neurogenic contractions were more sensitive to the local anaesthetics than those evoked by exogenous NA. The onset of inhibition was slow and developed gradually. This inhibition was concentration-dependent and continued for several hours in spite of repeated washings of the vessels. Pretreatment of the vascular preparations with pentacaine and heptacaine reduced NA- and Ca2+-induced contractions in Ca2+-free K+-depolarizing solution. The Ca2+-contracted vessels were also relaxed by the anaesthetics studied. It is suggested that carbamate local anaesthetics inhibit not only neuronal conductance but also Ca2+ entry into the vascular smooth muscle cells and NA-induced release of intracellular Ca2+.
在等长条件下,研究了氨基甲酸酯类局部麻醉药(喷他卡因和庚卡因)对离体兔血管中经壁神经刺激、外源性去甲肾上腺素(NA)和氯化钾诱导的收缩反应以及对去甲肾上腺素诱导的Ca2+动员的影响。喷他卡因和庚卡因抑制神经源性收缩以及外源性NA和氯化钾引起的收缩。神经源性收缩比外源性NA引起的收缩对局部麻醉药更敏感。抑制的起效缓慢且逐渐发展。这种抑制是浓度依赖性的,尽管对血管进行了反复冲洗,但仍持续数小时。用喷他卡因和庚卡因预处理血管制剂可降低无钙K+去极化溶液中NA和Ca2+诱导的收缩。所研究的麻醉药也使Ca2+收缩的血管舒张。提示氨基甲酸酯类局部麻醉药不仅抑制神经元传导,还抑制Ca2+进入血管平滑肌细胞以及NA诱导的细胞内Ca2+释放。