The Botulinum Treatment of Neurogenic Detrusor Overactivity: The Double-Face of the Neurotoxin

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 vesicula...

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Main Authors: Chiara Traini, Maria Giuliana Vannucchi
Format: Article
Language:English
Published: MDPI AG 2019-10-01
Series:Toxins
Subjects:
Online Access:https://www.mdpi.com/2072-6651/11/11/614
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spelling doaj-bcbf5232e7d0436e9a3d8ef3de9b6df42020-11-25T02:28:31ZengMDPI AGToxins2072-66512019-10-01111161410.3390/toxins11110614toxins11110614The Botulinum Treatment of Neurogenic Detrusor Overactivity: The Double-Face of the NeurotoxinChiara Traini0Maria Giuliana Vannucchi1Department of Experimental and Clinical Medicine, Research Unit of Histology and Embryology, University of Florence, 50139 Florence, ItalyDepartment of Experimental and Clinical Medicine, Research Unit of Histology and Embryology, University of Florence, 50139 Florence, ItalyBotulinum 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.https://www.mdpi.com/2072-6651/11/11/614urinary bladderspinal cord lesionupper lamina propriadetrusorurotheliuminnervationsensory systemsafferent nerve endingsnerve sprouting
collection DOAJ
language English
format Article
sources DOAJ
author Chiara Traini
Maria Giuliana Vannucchi
spellingShingle Chiara Traini
Maria Giuliana Vannucchi
The Botulinum Treatment of Neurogenic Detrusor Overactivity: The Double-Face of the Neurotoxin
Toxins
urinary bladder
spinal cord lesion
upper lamina propria
detrusor
urothelium
innervation
sensory systems
afferent nerve endings
nerve sprouting
author_facet Chiara Traini
Maria Giuliana Vannucchi
author_sort Chiara Traini
title The Botulinum Treatment of Neurogenic Detrusor Overactivity: The Double-Face of the Neurotoxin
title_short The Botulinum Treatment of Neurogenic Detrusor Overactivity: The Double-Face of the Neurotoxin
title_full The Botulinum Treatment of Neurogenic Detrusor Overactivity: The Double-Face of the Neurotoxin
title_fullStr The Botulinum Treatment of Neurogenic Detrusor Overactivity: The Double-Face of the Neurotoxin
title_full_unstemmed The Botulinum Treatment of Neurogenic Detrusor Overactivity: The Double-Face of the Neurotoxin
title_sort botulinum treatment of neurogenic detrusor overactivity: the double-face of the neurotoxin
publisher MDPI AG
series Toxins
issn 2072-6651
publishDate 2019-10-01
description 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.
topic urinary bladder
spinal cord lesion
upper lamina propria
detrusor
urothelium
innervation
sensory systems
afferent nerve endings
nerve sprouting
url https://www.mdpi.com/2072-6651/11/11/614
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