Abstract

Botulinum neurotoxin (BoNT) can counteract the highly frequent involuntary muscle contractions and the uncontrolled micturition events that characterize the neurogenic detrusor overactivity (NDO) due to supra-sacral spinal cord lesions. The ability of the toxin to block the neurotransmitter vesicular release causes the reduction of contractions and improves the compliance of the muscle and the bladder filling. BoNT is the second-choice treatment for NDO once the anti-muscarinic drugs have lost their effects. However, the toxin shows a time-dependent efficacy reduction up to a complete loss of activity. The cellular mechanisms responsible for BoNT effects exhaustion are not yet completely defined. Similarly, also the sites of its action are still under identification. A growing amount of data suggest that BoNT, beyond the effects on the efferent terminals, would act on the sensory system recently described in the bladder mucosa. The specimens from NDO patients no longer responding to BoNT treatment displayed a significant increase of the afferent terminals, likely excitatory, and signs of a chronic neurogenic inflammation in the mucosa. In summary, beyond the undoubted benefits in ameliorating the NDO symptomatology, BoNT treatment might bring to alterations in the bladder sensory system able to shorten its own effectiveness.

Highlights

  • Botulinum neurotoxin (BoNT) represents one of the most powerful and versatile drugs currently available in the pharmaceutical market

  • The perception of the bladder state is ensured by an integrated system encompassing the urothelium, the underlying lamina propria (LP), namely the connective tissue between the transition epithelium and the detrusor, and the local afferent terminals (Figure 2A) including the entire mucosa [16,17,18,19,20]

  • All these results indicate the urothelium as a second site of BoNT subtype A (BoNT/A)

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Summary

Introduction

Botulinum neurotoxin (BoNT) represents one of the most powerful and versatile drugs currently available in the pharmaceutical market. It is effective and safe in the treatment of several disorders spanning among numerous medical specialties such as ophthalmology, orthopedy, dermatology, urology, pain medicine and plastic surgery [1,2,3,4,5,6]. As in the other fields of application, the BoNT/A treatment needs to be periodically repeated in NDO This necessity could depend on the compensatory nerve sprouting employed by the neurons to overcome the block of synaptic vesicular release caused by the toxin [12,13]. Emphasis will be placed on the changes observed in the sensory system in bladder specimens of NDO patients in which BoNT was no longer effective

Bladder Innervation
Sensory System
The Urothelium
The Lamina Propria
Bladder
Pathophysiology
First-Choice Therapy
Second-Choice Therapy
Toxins
Afferent Nerve Terminals
Urothelium
Lamina Propria
Cyclic BoNT Treatments Generate Substantial Changes in the Bladder Wall
Sprouting and Chronic Neurogenic Inflammation
Findings
Conclusions
Full Text
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