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A new approach to recording the electromyographic activity of detrusor smooth muscle.

机译:一种记录逼尿肌平滑肌肌电活动的新方法。

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PURPOSE: Extracellular recordings from the whole intact mammalian bladder of the electrical events leading to contraction of the organ have been elusive for almost 50 years despite the widespread potential applications of such a technique. The principal problem is the need to isolate the small real signals reflecting membrane depolarization from the large electromechanical artifact generated as the organ contracts. In this preliminary study we determined whether electrical signals may be isolated and verified as biological using extracellular bipolar reversible suction electrodes. MATERIALS AND METHODS: Six whole excised guinea pig bladders were mounted in an especially constructed organ bath. Electrical activity resulting from nerve stimulation of the organ was recorded using a novel 10 bipolar Pt/PtCl suction electrode simultaneously with changes in intravesical pressure. Mechanical and pharmacological control experiments were performed to determine the true origin of these signals. RESULTS: A predominantly biphasic electrical signal of a mean amplitude plus or minus standard deviation of 647 plus or minus 301 microV. and a mean duration of 293 plus or minus 51 milliseconds was consistently recorded from the serosal surface of all guinea pig bladders. In all cases the electrical signal and mechanical response to stimulation were completely abolished by 1 microM. tetrodotoxin. The signal always preceded any change in intravesical pressure. It was sensitive to changes in the CaCl2 concentration of the superfusate, abolished by purinergic but not cholinergic neuromuscular blockade and independent of electromechanical artifact. CONCLUSIONS: In this preliminary report we describe a novel technique by which nerve mediated detrusor electrical activity leading to contraction of the whole intact guinea pig bladder may be isolated from artifact and verified as real. We hope that development of this technique may enable its application to the in situ human bladder. However, to our knowledge whether electromyographic activity may be recorded from human detrusor remains to be determined.
机译:目的:尽管这种技术具有广泛的潜在应用前景,但从整个完整的哺乳动物膀胱中导致器官收缩的电事件的细胞外记录已难以捉摸。主要问题是需要将反映膜去极化的小真实信号与随着器官收缩而产生的大机电伪像隔离开来。在这项初步研究中,我们确定了是否可以使用细胞外双极可逆吸引电极来隔离电信号并将其验证为生物学信号。材料与方法:将六个完整切除的豚鼠膀胱安装在特别构造的器官浴中。使用新颖的10双极Pt / PtCl吸引电极同时记录膀胱内压力的变化,记录由器官的神经刺激引起的电活动。进行了机械和药理控制实验,以确定这些信号的真实来源。结果:主要为双相电信号,平均振幅为正负647微弱或301微伏的标准差。并且从所有豚鼠膀胱的浆膜表面持续记录的平均持续时间为293±51毫秒。在所有情况下,对电刺激的电信号和机械响应均被1 microM完全消除。河豚毒素。信号总是在任何膀胱内压力变化之前发生。它对超融合物中CaCl2浓度的变化敏感,而嘌呤能而非胆碱能神经肌肉阻滞消除了该作用,并且与机电伪影无关。结论:在这份初步报告中,我们描述了一种新技术,通过该技术,可以从人工制品中分离出导致整个完整豚鼠膀胱收缩的神经介导的逼尿肌电活动,并将其验证为真实的。我们希望这项技术的发展可以使其应用于原位人类膀胱。然而,据我们所知,是否可以从人类逼尿肌记录肌电活动尚待确定。

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