Santicioli P, Maggi C A
Pharmacology Department, Menarini Ricerche s.p.a., Via Rismondo 12A, 50131, Florence Italy.
Br J Pharmacol. 2000 Jan;129(1):163-9. doi: 10.1038/sj.bjp.0703004.
We have tested the effect of the gap junction inhibitor, 18beta-glycyrrhetinic acid (18betaGA) on electromechanical coupling in the guinea-pig renal pelvis and ureter by the sucrose gap technique. In the ureter 18betaGA (3 - 30 microM) produced a concentration-dependent inhibition of the spike component of the action potential (AP) and reduced contraction evoked by electrical stimulation. Neurokinin A (NKA) produced a slow depolarization with superimposed APs and phasic contractions of the ureter. 18betaGA (30 microM) markedly inhibited the depolarization and APs evoked by NKA. However the contractile response was more sustained in the presence than in the absence of 18betaGA. At 100 microM, 18betaGA inhibited the mechanical responses to NKA. KCl (80 mM) produced APs and phasic contractions followed by sustained depolarization and tonic contraction. At 30 microM 18betaGA markedly inhibited the KCl-evoked APs and phasic contractions without affecting the sustained responses. At 100 microM 18betaGA inhibited the tonic contraction to KCl. In the renal pelvis 18betaGA (30 microM) inhibited the amplitude of pacemaker potentials and accompanying contractions and induced the appearance of low-amplitude APs not associated with contraction. We conclude that, up to 30 microM, the action of 18betaGA is consistent with an inhibition of cell-to-cell electrical coupling via gap junctions. The single-unit character of smooth muscles in the guinea-pig upper urinary tract is partly converted to a multi-unit pattern. At high concentrations 18betaGA possesses non specific effects which limit its usefulness as a tool for studying the role of gap junctions in smooth muscles. British Journal of Pharmacology (2000) 129, 163 - 169
我们通过蔗糖间隙技术,测试了缝隙连接抑制剂18β-甘草次酸(18βGA)对豚鼠肾盂和输尿管机电耦联的影响。在输尿管中,18βGA(3 - 30微摩尔)对动作电位(AP)的锋电位成分产生浓度依赖性抑制,并减弱电刺激诱发的收缩。神经激肽A(NKA)使输尿管产生缓慢去极化,并伴有叠加的AP和相性收缩。18βGA(30微摩尔)显著抑制NKA诱发的去极化和AP。然而,与不存在18βGA时相比,存在18βGA时收缩反应更持久。在100微摩尔时,18βGA抑制对NKA的机械反应。氯化钾(80毫摩尔)产生AP和相性收缩,随后是持续去极化和强直性收缩。在30微摩尔时,18βGA显著抑制氯化钾诱发的AP和相性收缩,而不影响持续反应。在100微摩尔时,18βGA抑制对氯化钾的强直性收缩。在肾盂中,18βGA(30微摩尔)抑制起搏电位的幅度和伴随的收缩,并诱导出现与收缩无关的低幅度AP。我们得出结论,在高达30微摩尔时,18βGA的作用与通过缝隙连接抑制细胞间电耦联一致。豚鼠上尿路平滑肌的单单位特性部分转变为多单位模式。在高浓度时,18βGA具有非特异性作用,这限制了其作为研究缝隙连接在平滑肌中作用工具的实用性。《英国药理学期刊》(2000年)129卷,163 - 169页