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首页> 外文期刊>Neurourology and urodynamics. >Effects of local anesthetics on human bladder contractility.
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Effects of local anesthetics on human bladder contractility.

机译:局麻药对人膀胱收缩力的影响。

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AIMS: We investigated the invitro effects of local anesthetics on the contractility of the human bladder. METHODS: By measuring the invitro isometric contractions of human bladder strips, we determined the effects of tetracaine, bupivacaine, lidocaine, and ropivacaine on the basal spontaneous contractions and contractions induced by various stimuli, namely, KCl (60 mM), carbachol (CCh), and electrical field stimulation (EFS). The effect of local anesthetic agents on Ca(2+)-independent sustained tonic contraction (SuTC) of the detrusor was also investigated. RESULTS: Local anesthetics increased phasic and tonic spontaneous contractile activity dose dependently in the concentration range 1-500 muM, but abolished phasic activity at higher concentrations. Local anesthetic agents inhibited nerve-mediated contraction (EFS, 0.8 msec) in a concentration-dependent manner (ropivacaine > tetracaine = bupivacaine > lidocaine), and inhibited non-nerve mediated contractions induced by KCl, long pulse EFS (direct muscle stimulation, 100 msec), and CCh. Inhibitory potency on non-nerve mediated contraction was for long pulse EFS: ropivacaine = tetracaine > bupivacaine = lidocaine and for KCl- and CCh-induced contractions: ropivacaine > tetracaine > bupivacaine = lidocaine. Higher concentrations of local anesthetics were needed to inhibit non-nerve-mediated bladder contraction than nerve-mediated contraction. SuTC was suppressed by all local anesthetics concentration dependently. CONCLUSIONS: Our study demonstrates that local anesthetics have inhibitory effects on the contraction of human bladder as induced by different stimulants and concentrations. Their effects and differences suggest that they may be considered potentially useful as diagnostic and therapeutic agents for bladder dysfunction.
机译:目的:我们研究了局部麻醉剂对人膀胱收缩性的体外影响。方法:通过测量人体膀胱条的体外等距收缩,我们确定了丁卡因,布比卡因,利多卡因和罗哌卡因对各种刺激(即KCl(60 mM),卡巴胆碱(CCh))引起的基础自发性收缩和收缩的影响。 ,以及电场刺激(EFS)。还研究了局部麻醉药对逼尿肌Ca(2+)依赖性持续性强直性收缩(SuTC)的影响。结果:局部麻醉药在1-500μM浓度范围内依赖性地增加了阶段性和强直性自发性收缩活动剂量,但在较高的浓度下取消了阶段性活动。局部麻醉药以浓度依赖性方式(罗哌卡因>丁卡因=布比卡因>利多卡因)抑制神经介导的收缩(EFS,0.8毫秒),并抑制由KCl,长脉冲EFS(直接肌肉刺激,100)引起的非神经介导的收缩毫秒)和CCh。长脉冲EFS对非神经介导的收缩的抑制作用为:罗哌卡因=丁卡因>布比卡因=利多卡因,以及KCl和CCh诱导的收缩:罗哌卡因>丁卡因>布比卡因=利多卡因。与神经介导的收缩相比,抑制非神经介导的膀胱收缩需要更高浓度的局麻药。所有局部麻醉药浓度均会抑制SuTC。结论:我们的研究表明,局部麻醉药对不同刺激物和浓度引起的人膀胱收缩具有抑制作用。它们的作用和差异表明,它们可能被视为潜在的有用的膀胱功能障碍的诊断和治疗药物。

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