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Interaction between neurotransmitter antagonists and effects of sacral neuromodulation in rats with chronically hyperactive bladder.

机译:神经递质拮抗剂之间的相互作用和chronic亢性慢性大鼠rats神经调节的影响。

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OBJECTIVE To investigate to what extent antagonists of spinal neurotransmitters interact with the effects of sacral neuromodulation in a rat model of a chronically hyperactive urinary bladder. MATERIALS AND METHODS In female rats the urinary bladder was instilled with turpentine oil 2.5% to induce cystitis. After surviving for 10 days the rats were anaesthetized with urethane, the bladder catheterized and connected to a pressure transducer. Stimulating electrodes were placed in the sacral foramina bilaterally. The spinal cord was exposed by a laminectomy, and a small pool was placed on the cord for intrathecal administration of neurotransmitter antagonists. Sacral neuromodulation was applied before and after administering the antagonists. The antagonists used were: memantine, an antagonist for N-methyl- d-aspartate (NMDA) receptors; CNQX, an antagonist for non-NMDA receptors, and L-NAPNA, a blocker of nitric oxide synthase. RESULTS With no electrical neuromodulation, memantine and L-NAPNA abolished thecystitis-induced bladder contractions for approximately 4 and approximately 37 min, respectively. The effect of CNQX was similar to that of artificial cerebrospinal fluid. Electrical sacral modulation with no antagonists also transiently abolished the bladder contractions; at the highest intensity used, the pause was 2-3 min. Superfusion of the spinal cord with CNQX reduced this effect of neuromodulation significantly, whereas memantine had no influence, and L-NAPNA increased the neuromodulation-induced pause. CONCLUSIONS The results suggest that non-NMDA receptors are involved in the effects of sacral neuromodulation, whereas NMDA receptors appear to have no role. Nitric oxide is essential for maintaining the chronic hyperactive state of the urinary bladder.
机译:目的探讨在慢性膀胱过度活动症大鼠模型中,脊髓神经递质拮抗剂在多大程度上与神经调节作用相互作用。材料与方法在雌性大鼠的膀胱中,向其注入2.5%松节油以诱发膀胱炎。存活10天后,用氨基甲酸乙酯麻醉大鼠,将其导尿并连接到压力传感器。将刺激电极两侧置于bilateral骨孔中。通过椎板切除术暴露脊髓,并在脊髓上放置一小池用于鞘内施用神经递质拮抗剂。在施用拮抗剂之前和之后均进行神经调节。使用的拮抗剂是:美金刚,N-甲基-d-天冬氨酸(NMDA)受体的拮抗剂;美金刚。 CNQX是非NMDA受体的拮抗剂,L-NAPNA是一氧化氮合酶的阻滞剂。结果在没有电神经调节的情况下,美金刚和L-NAPNA分别消除了由膀胱炎引起的膀胱收缩约4分钟和约37分钟。 CNQX的作用类似于人工脑脊液。没有拮抗剂的骨电调制也可以暂时消除膀胱收缩。在使用的最高强度下,暂停时间为2-3分钟。脊髓与CNQX的融合显着降低了这种神经调节作用,而美金刚没有影响,而L-NAPNA则增加了神经调节引起的停顿。结论结果提示非NMDA受体参与神经调节的作用,而NMDA受体似乎没有作用。一氧化氮对于维持膀胱的慢性过度活跃状态至关重要。

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