Magura I S
Br J Pharmacol. 1986 Jul;88(3):523-30. doi: 10.1111/j.1476-5381.1986.tb10232.x.
The effects of local anaesthetic tertiary amines (procaine, lignocaine and tetracaine) as well as neutral (benzocaine) and permanently charged (QX-314) local anaesthetics were studied on the evoked electrical and mechanical activity of the ureter smooth muscle. 'Low' concentrations of procaine and lignocaine (0.1-1mM) at pH 7.4 increased the duration of the slow plateau component of the evoked action potentials. The amplitude of the phasic contraction was consequently increased within the first 5 min of exposure. Tetracaine 0.1 mM caused a transient increase in the duration of the plateau and amplitude of the phasic contraction within the first 1-2 min only. The stimulant action of the local anaesthetics was greatly reduced in the presence of tetraethylammonium (TEA). All the tertiary local anaesthetics caused depolarization of the membrane accompanied by an increase in the size of the electronic potentials. Lignocaine normally initiated the discharge of spontaneous action potentials. High concentrations of lignocaine (5 mM) and tetracaine (0.5 mM) caused complete inhibition of the evoked action potentials and phasic contractions. Procaine 5 mM predominantly inhibited the contractile responses. The permanently charged local anaesthetic QX-314 (1 mM) caused an increase in the duration and amplitude of the plateau, increasing the number of spikes and the amplitude and duration of the phasic contraction. It also depolarized the ureter smooth muscle cells increasing the size of electronic potentials. The neutral local anaesthetic benzocaine at 1 mM caused a reversible selective blockade of the plateau component of the evoked action potential and a gradual reduction in the amplitude of the phasic contraction. No change in either the membrane potential or the membrane conductance was observed. 7 High pH. (pH 9) significantly increased while low pH0 (pH 6) decreased the inhibitory action of procaine and lignocaine but did not alter the effects of benzocaine and QX-314. 8 Benzocaine caused a relaxation of the high-K-induced contraction, preferentially blocking the tonic component, whereas QX-314 had no effect on the KC1-contracture of the ureter muscle. 9 Two sites of action in the ureter smooth muscle cell membrane for local anaesthetics are suggested. One site interacts with local anaesthetics in a charged form, while the other one interacts with those in a lipid-soluble neutral form. The charged form of local anaesthetics has a TEA-like action, while the neutral form predominantly causes blockade of 'slow' Na/Ca channels.
研究了局部麻醉叔胺类药物(普鲁卡因、利多卡因和丁卡因)以及中性(苯佐卡因)和带永久电荷(QX - 314)的局部麻醉药对输尿管平滑肌诱发的电活动和机械活动的影响。在pH 7.4条件下,“低”浓度的普鲁卡因和利多卡因(0.1 - 1 mM)可增加诱发动作电位缓慢平台期的持续时间。因此,在暴露的前5分钟内,相性收缩的幅度增加。0.1 mM的丁卡因仅在最初1 - 2分钟内使平台期持续时间和相性收缩幅度短暂增加。在四乙铵(TEA)存在的情况下,局部麻醉药的刺激作用大大降低。所有叔胺类局部麻醉药均引起膜去极化,同时伴随电紧张电位大小增加。利多卡因通常引发自发动作电位的发放。高浓度的利多卡因(5 mM)和丁卡因(0.5 mM)可完全抑制诱发的动作电位和相性收缩。5 mM的普鲁卡因主要抑制收缩反应。带永久电荷的局部麻醉药QX - 314(1 mM)使平台期的持续时间和幅度增加,增加了峰电位数量以及相性收缩的幅度和持续时间。它还使输尿管平滑肌细胞去极化,增加电紧张电位的大小。1 mM的中性局部麻醉药苯佐卡因可对诱发动作电位的平台期成分产生可逆性选择性阻断,并使相性收缩幅度逐渐降低。未观察到膜电位或膜电导的变化。7高pH(pH 9)显著增强而低pH(pH 6)降低普鲁卡因和利多卡因的抑制作用,但不改变苯佐卡因和QX - 314的作用。8苯佐卡因可使高钾诱导的收缩松弛,优先阻断紧张性成分,而QX - 314对输尿管肌肉的氯化钾挛缩无影响。9提出了局部麻醉药在输尿管平滑肌细胞膜上的两个作用位点。一个位点与带电荷形式的局部麻醉药相互作用,而另一个位点与脂溶性中性形式的局部麻醉药相互作用。局部麻醉药的带电荷形式具有类似TEA的作用,而中性形式主要导致“慢”钠/钙通道的阻断。