脊髓损伤后下尿路功能障碍的最新知识和新领域:基础研究观点。

IF 0.8 Q4 UROLOGY & NEPHROLOGY Urological Science Pub Date : 2022-07-01 Epub Date: 2022-08-25 DOI:10.4103/uros.uros_31_22
Naoki Wada, Sergei Karnup, Katsumi Kadekawa, Nobutaka Shimizu, Joonbeom Kwon, Takahiro Shimizu, Daisuke Gotoh, Hidehiro Kakizaki, William C de Groat, Naoki Yoshimura
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引用次数: 15

摘要

本文综述了骶部以上脊髓损伤(SCI)后下尿路功能障碍(LUTD)的基础研究进展。我们特别关注控制下尿路(LUT)功能的神经生理机制以及SCI诱导的SCI动物模型排尿控制的变化。LUT有两个主要功能,尿液的储存和排泄,由一个复杂的神经控制系统调节。该神经系统协调LUT中两个功能单元的活动:膀胱和出口,包括膀胱颈、尿道和盆底横纹肌。在储尿期,出口关闭,膀胱处于静止状态,以维持膀胱内低压力和节制;在排尿期,出口放松,膀胱收缩,促进尿液有效释放。脊髓损伤损害了排尿的自主控制以及协调膀胱和括约肌功能的正常反射通路。脊髓损伤后,膀胱最初是反射性的,但随后由于脊髓排尿反射通路的出现而变得高反射性。然而,由于膀胱和尿道括约肌之间的协调丧失,膀胱不能有效排空。在脊髓损伤动物模型中,沉默c纤维膀胱传入神经的高兴奋性是神经源性LUTD的主要病理生理基础,尤其是逼尿肌过度活动。反射可塑性与神经肽、神经营养因子或传入神经元化学受体的特性变化有关。除c -纤维外,a -纤维也可能参与脊髓损伤后逼尿肌括约肌协同障碍等神经源性LUTD的发生。使用疾病模型的动物研究有助于我们发现脊髓损伤所致LUTD的不同影响因素,并找到新治疗的潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Current Knowledge and Novel Frontiers in Lower Urinary Tract Dysfunction after Spinal Cord Injury: Basic Research Perspectives.

This review article aims to summarize the recent advancement in basic research on lower urinary tract dysfunction (LUTD) following spinal cord injury (SCI) above the sacral level. We particularly focused on the neurophysiologic mechanisms controlling the lower urinary tract (LUT) function and the SCI-induced changes in micturition control in animal models of SCI. The LUT has two main functions, the storage and voiding of urine, that are regulated by a complex neural control system. This neural system coordinates the activity of two functional units in the LUT: the urinary bladder and an outlet including bladder neck, urethra, and striated muscles of the pelvic floor. During the storage phase, the outlet is closed and the bladder is quiescent to maintain a low intravesical pressure and continence, and during the voiding phase, the outlet relaxes and the bladder contracts to promote efficient release of urine. SCI impairs voluntary control of voiding as well as the normal reflex pathways that coordinate bladder and sphincter function. Following SCI, the bladder is initially areflexic but then becomes hyperreflexic due to the emergence of a spinal micturition reflex pathway. However, the bladder does not empty efficiently because coordination between the bladder and urethral sphincter is lost. In animal models of SCI, hyperexcitability of silent C-fiber bladder afferents is a major pathophysiological basis of neurogenic LUTD, especially detrusor overactivity. Reflex plasticity is associated with changes in the properties of neuropeptides, neurotrophic factors, or chemical receptors of afferent neurons. Not only C-fiber but also Aδ-fiber could be involved in the emergence of neurogenic LUTD such as detrusor sphincter dyssynergia following SCI. Animal research using disease models helps us to detect the different contributing factors for LUTD due to SCI and to find potential targets for new treatments.

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来源期刊
Urological Science
Urological Science UROLOGY & NEPHROLOGY-
CiteScore
1.20
自引率
0.00%
发文量
26
审稿时长
6 weeks
期刊最新文献
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