Abstract

The recent surge in research on cannabinoids may have been fueled by changes in legislation in several jurisdictions, and by approval for the use of cannabinoids for treatment of some chronic diseases. Endocannabinoids act largely, but not exclusively on cannabinoid receptors 1 and 2 (CBR1 and CBR2) which are expressed in the bladder mainly by the urothelium and the axons and endings of motor and sensory neurons. A growing body of evidence suggests that endocannabinoid system constitutively downregulates sensory bladder function during urine storage and micturition, under normal physiological conditions. Similarly, exogenous cannabinoid agonists have potent modulatory effects, as do inhibitors of endocannabinoid inactivation. Results suggest a high potential of cannabinoids to therapeutically ameliorate lower urinary tract symptoms in overactive bladder and painful bladder syndromes. At least part of this may be mediated via effects on sensory nerves, although actions on efferent nerves complicate interpretation. The sensory innervation of bladder is complex with at least eight classes identified. There is a large gap in our knowledge of the effects of endocannabinoids and synthetic agonists on different classes of bladder sensory neurons. Future studies are needed to reveal the action of selective cannabinoid receptor 2 agonists and/or peripherally restricted synthetic cannabinoid receptor 1 agonists on bladder sensory neurons in animal models of bladder diseases. There is significant potential for these novel therapeutics which are devoid of central nervous system psychotropic actions, and which may avoid many of the side effects of current treatments for overactive bladder and painful bladder syndromes.

Highlights

  • The endocannabinoid system (ECS) consists of several endocannabinoids and their G-protein coupled receptors (GPCRs) together with synthetizing and degradation enzymes which are present in nearly every bodily tissue including bladder and dorsal root ganglion (DRG) neurons (Merriam et al, 2011; Strittmatter et al, 2012; Bakali et al, 2013; Izzo et al, 2015; Hedlund and Gratzke, 2016; Bjorling and Wang, 2018)

  • Despite some discrepancies in the expression of CBR1/CBR2 and the effects of exogenous and endogenous cannabinoids on sensory neurons and micturition in naive bladders and in animal models of overactive bladder (OAB) and painful bladder syndromes (PBS), preclinical research has identified the significant potential of cannabinoids as novel treatments for common bladder disorders

  • Use of fatty acid amide hydrolase (FAAH) and other inhibitors to elevate the level of endogenous endocannabinoids currently appears less attractive since the action of endocannabinoids is complicated by off-target effects on ligand and voltage-gated channels, low efficacy, and possible side effects

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Summary

Introduction

The endocannabinoid system (ECS) consists of several endocannabinoids and their G-protein coupled receptors (GPCRs) together with synthetizing and degradation enzymes which are present in nearly every bodily tissue including bladder and dorsal root ganglion (DRG) neurons (Merriam et al, 2011; Strittmatter et al, 2012; Bakali et al, 2013; Izzo et al, 2015; Hedlund and Gratzke, 2016; Bjorling and Wang, 2018). The non-selective CBR1/CBR2 agonist AZ12646915 reduces distension-evoked firing of high-threshold pelvic afferents in mouse bladder via CBR1 (Walczak et al, 2009). A non-selective cannabinoid agonist, ajulemic acid, reduces ATP- and capsaicin-evoked release of CGRP in the rat bladder; an effect reversed by both CB1 and CB2 antagonists, AM252 and AM630 (Hayn et al, 2008).

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