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首页> 外文期刊>Neurourology and urodynamics. >Impaired micturition reflex caused by acute selective dorsal or ventral root(s) rhizotomy in anesthetized rats.
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Impaired micturition reflex caused by acute selective dorsal or ventral root(s) rhizotomy in anesthetized rats.

机译:麻醉大鼠急性选择性背侧或腹侧根部切开术引起的排尿反射受损。

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摘要

PURPOSE: To clarify the contributions of parasympathetic inputs and outputs to the micturition reflex. MATERIALS AND METHODS: Intra-vesical pressure (IVP), external urethral sphincter electromyogram (EMG), pelvic afferent nerve activities (PANA), and pelvic efferent nerve activities (PENA) as well as the time-derived IVP (dIVP, an index of bladder contractility) were evaluated in intact and acute dorsal or ventral root(s) rhizotomized (DRX and VRX, respectively) rats. RESULTS: In DRX rats, when compared with that in intact stage, the voiding frequency was decreased (75 +/- 15% of intact, P < 0.05, n = 8), while the threshold pressure to trigger voiding contractions was significantly increased (187 +/- 75% of intact, P < 0.05, n = 8). In addition, several insufficient contractions (5.3 +/- 3.5 contractions/voiding, P < 0.05, n = 8) occurred in ahead of each voiding contraction. On the other hand, in VRX rats, the peak and rebound IVP were significantly decreased (90 +/- 3.5% and 75 +/- 11.3% of intact, P < 0.01, n = 8), while the threshold pressure was not affected (102 +/- 11% of intact, P = NS, n = 8). The time-derived parameters were significantly decreased in VRX (peak dIVP, 78 +/- 10.2%, rebound dIVP, 75 +/- 15.6%, minimal dIVP, 68 +/- 14% of intact, P < 0.01, n = 8) but only peak dIVP was decreased (85 +/- 11% of intact, P < 0.01, n 8) in DRX rats. CONCLUSION: Acute selective DRX and VRX rat can be an animal model to investigate peripheral neural control in micturition functions.
机译:目的:阐明副交感神经输入和输出对排尿反射的贡献。材料与方法:膀胱内压(IVP),尿道外括约肌肌电图(EMG),盆腔传入神经活动(PANA)和盆腔传入神经活动(PENA)以及时间衍生的IVP(dIVP,指数在完整的和急性的背根或腹根切开的大鼠(分别为DRX和VRX)中评估了膀胱的收缩能力)。结果:与完整期相比,DRX大鼠的排尿频率降低(完整期的75 +/- 15%,P <0.05,n = 8),而触发排尿收缩的阈值压力显着增加(完整的187 +/- 75%,P <0.05,n = 8)。此外,在每次排尿收缩之前,出现了几次不充分的收缩(5.3 +/- 3.5收缩/无效,P <0.05,n = 8)。另一方面,在VRX大鼠中,峰值和反弹IVP显着降低(完整的90 +/- 3.5%和75 +/- 11.3%,P <0.01,n = 8),而阈值压力不受影响(完整的102 +/- 11%,P = NS,n = 8)。 VRX中时间参数显着降低(峰值dIVP,78 +/- 10.2%,回弹dIVP,75 +/- 15.6%,最小dIVP,完整的68 +/- 14%,P <0.01,n = 8 ),但在DRX大鼠中只有dIVP峰值降低(完整的85 +/- 11%,P <0.01,n 8)。结论:急性选择性DRX和VRX大鼠可以作为研究排尿功能周围神经控制的动物模型。

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