Hypolite Joseph A, Malykhina Anna P
Division of Urology, Department of Surgery, University of Colorado Denver, Anschutz Medical Campus, 12700 E 19th Ave. Mail Stop C317, Aurora, CO, 80045, USA.
BMC Urol. 2015 Nov 4;15:110. doi: 10.1186/s12894-015-0106-6.
Protein kinase C (PKC) is expressed in many tissues and organs including the urinary bladder, however, its role in bladder physiology and pathophysiology is still evolving. The aim of this review was to evaluate available evidence on the involvement of PKC in regulation of detrusor contractility, muscle tone of the bladder wall, spontaneous contractile activity and bladder function under physiological and pathophysiological conditions.
This is a non-systematic review of the published literature which summarizes the available animal and human data on the role of PKC signaling in the urinary bladder under different physiological and pathophysiological conditions. A wide PubMed search was performed including the combination of the following keywords: "urinary bladder", "PKC", "detrusor contractility", "bladder smooth muscle", "detrusor relaxation", "peak force", "detrusor underactivity", "partial bladder outlet obstruction", "voltage-gated channels", "bladder nerves", "PKC inhibitors", "PKC activators". Retrieved articles were individually screened for the relevance to the topic of this review with 91 citations being selected and included in the data analysis.
Urinary bladder function includes the ability to store urine at low intravesical pressure followed by a subsequent release of bladder contents due to a rapid phasic contraction that is maintained long enough to ensure complete emptying. This review summarizes the current concepts regarding the potential contribution of PKC to contractility, physiological voiding, and related signaling mechanisms involved in the control of both the storage and emptying phases of the micturition cycle, and in dysfunctional voiding. Previous studies linked PKC activation exclusively with an increase in generation of the peak force of smooth muscle contraction, and maximum force generation in the lower urinary tract. More recent data suggests that PKC presents a broader range of effects on urinary bladder function including regulation of storage, emptying, excitability of the detrusor, and bladder innervation. In this review, we evaluated the mechanisms of peripheral and local regulation of PKC signaling in the urinary bladder, and their impact on different phases of the micturition cycle under physiological and pathophysiological conditions.
蛋白激酶C(PKC)在包括膀胱在内的许多组织和器官中均有表达,然而,其在膀胱生理和病理生理中的作用仍在不断演变。本综述的目的是评估现有证据,以探讨PKC在生理和病理生理条件下对逼尿肌收缩力、膀胱壁肌张力、自发收缩活动及膀胱功能调节中的作用。
这是一篇对已发表文献的非系统性综述,总结了不同生理和病理生理条件下PKC信号在膀胱中作用的现有动物和人体数据。通过PubMed进行了广泛检索,检索词组合如下:“膀胱”、“PKC”、“逼尿肌收缩力”、“膀胱平滑肌”、“逼尿肌舒张”、“峰值力”、“逼尿肌活动低下”、“膀胱出口部分梗阻”、“电压门控通道”、“膀胱神经”、“PKC抑制剂”、“PKC激活剂”。对检索到的文章逐一筛选与本综述主题的相关性,共选择91篇引文纳入数据分析。
膀胱功能包括在膀胱内压低时储存尿液的能力,随后由于快速的阶段性收缩而排出膀胱内容物,这种收缩持续足够长的时间以确保完全排空。本综述总结了关于PKC对收缩力、生理性排尿以及参与排尿周期储存和排空阶段控制及排尿功能障碍的相关信号机制潜在贡献的当前概念。先前的研究仅将PKC激活与平滑肌收缩峰值力的增加以及下尿路最大力的产生联系起来。最近的数据表明,PKC对膀胱功能具有更广泛的影响,包括对储存、排空、逼尿肌兴奋性和膀胱神经支配的调节。在本综述中,我们评估了膀胱中PKC信号的外周和局部调节机制,以及它们在生理和病理生理条件下对排尿周期不同阶段的影响。