Abstract

Relaxation and contraction of the urinary bladder smooth muscle, also known as the detrusor smooth muscle (DSM), facilitate the micturition cycle. DSM contractility depends on cell excitability, which is established by the synchronized activity of multiple diverse ion channels. K+ channels, the largest family of channels, control DSM excitability by maintaining the resting membrane potential and shaping the action potentials that cause the phasic contractions. Among the members of the voltage-gated K+ (KV) channel superfamily, KV type 7 (KV7) channels — KV7.1–KV7.5 members encoded by KCNQ1–KCNQ5 genes — have been recently identified as functional regulators in various cell types including vascular, cardiac, and neuronal cells. Their regulatory roles in DSM, however, are just now emerging and remain to be elucidated. To address this gap, our research group has initiated the systematic investigation of human DSM KV7 channels in collaboration with clinical urologists. In this comprehensive review, we summarize the current understanding of DSM Kv7 channels and highlight recent discoveries in the field. We describe KV7 channel expression profiles at the mRNA and protein levels, and further elaborate on functional effects of KV7 channel selective modulators on DSM excitability, contractility, and intracellular Ca2+ dynamics in animal species along with in vivo studies and the limited data on human DSM. Within each topic, we highlight the main observations, current gaps in knowledge, and most pressing questions and concepts in need of resolution. We emphasize the lack of systematic studies on human DSM KV7 channels that are now actively ongoing in our laboratory.

Highlights

  • The urinary bladder smooth muscle, referred to as the detrusor smooth muscle (DSM) forms the bladder wall and determines the two fundamental functions of the organ: urine storage and voiding (Andersson and Arner, 2004; Andersson and Wein, 2004)

  • We summarize the expression profiles for KV type 7 (KV7) channel subtypes in DSM whole-tissue and single-cell preparations, electrophysiological findings for KV7 channel modulators in DSM cell patch-clamp and tissue conventional microelectrode electrophysiological experiments, and how KV7 channel pharmacological modulators affect intracellular Ca2+ concentrations and DSM contractility

  • We found that intracellular Ca2+ concentration in DSM tissue and cells, imaged by Fura-2AM, was decreased following the application of two subtype-preferential KV7 channel activators, ICA-069673 (Provence et al, 2015) and ML213 (Provence et al, 2018)

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Summary

Introduction

The urinary bladder smooth muscle, referred to as the detrusor smooth muscle (DSM) forms the bladder wall and determines the two fundamental functions of the organ: urine storage and voiding (Andersson and Arner, 2004; Andersson and Wein, 2004). Elevation of extracellular K+ from 5 or 20 to 60 mM reduced retigabine-, ICA-069673-, and ML213-induced relaxation in rat or guinea pig DSM strips, consistent with a K+ conductance underlying the effect of these KV7 channel activators on DSM contractility (Argentieri and Sheldon, 2006; Rode et al, 2010; Provence et al, 2015).

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