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Resiniferatoxin and botulinum toxin type A for treatment of lower urinary tract symptoms
Author(s) -
Cruz Francisco,
Dinis Paulo
Publication year - 2007
Publication title -
neurourology and urodynamics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 90
eISSN - 1520-6777
pISSN - 0733-2467
DOI - 10.1002/nau.20479
Subject(s) - resiniferatoxin , medicine , interstitial cystitis , overactive bladder , urinary urgency , botulinum toxin , urinary incontinence , urology , urinary system , urinary bladder , detrusor muscle , trpv1 , receptor , anesthesia , transient receptor potential channel , pathology , alternative medicine
Resiniferatoxin (RTX) and botulinum toxin subtype A (BTX‐A) are increasingly viewed as potential treatments for lower urinary tract symptoms (LUTS) refractory to conventional therapy. RTX, a capsaicin analogue devoid of severe pungent properties, acts by desensitizing the transient receptor potential vanilloid type 1 (TRPV1) receptor and inactivating C‐fibers. BTX‐A cleaves soluble N‐ethylmaleimide‐sensitive factor attachment protein receptor (SNARE) proteins in afferent and efferent nerve endings, therefore impeding the fusion of synaptic vesicles with the neuronal membrane necessary for the release of neurotransmitters. In patients with neurogenic and idiopathic detrusor overactivity, RTX and BTX‐A have been shown to increase the volume to first detrusor contraction, increase bladder capacity, and improve urinary incontinence and quality of life. Recent data also suggest a role for these neurotoxins in treating urgency, the primary symptom in overactive bladder (OAB) syndrome. Furthermore, experimental data strongly support the use of both neurotoxins in the treatment of pain and frequency in patients with interstitial cystitis/painful bladder syndrome (IC/PBS), although the results from available clinical trials for this use are still inconclusive. In spite of promising results overall, it should be made clear that the administration of these neurotoxins is still considered an experimental procedure and that more clinical studies are necessary before a license for their use will be issued by health authorities. Neurourol. Urodynam. 26:920–927, 2007. © 2007 Wiley‐Liss, Inc.