Abstract
Increased voiding frequency and urgency are among the most prevalent storage lower urinary tract symptoms (LUTS), often diagnosed as part of overactive bladder syndrome (OAB). It has been suggested that these symptoms are caused by excessive sensory activation of the neural micturition circuit. It seems likely that sensory pathway remodelling is also responsible for pain perception upon bladder filling in patients with bladder pain syndrome (BPS). Neurotrophins—including nerve growth factor (NGF), brain-derived nerve factor (BDNF), neurotrophin-3 (NT-3) and neurotrophin-4 (NT-4)—represent master modulators of neural plasticity, both in peripheral and central nervous systems. Accumulating evidence points towards a role for neurotrophins in the control of neural sensory function during micturition and indicates their involvement in the emergence of OAB-related and BPS-related LUTS. Neurotrophins could potentially be used as urinary biomarkers to improve diagnostic accuracy for OAB and BPS and monitor therapy effectiveness. Proof-of-principle clinical evidence has confirmed that NGF is a potential target for treating human bladder overactivity.
Key Points
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Urgency, frequency and bladder pain are all associated with hypersensitization and remodelling of bladder peripheral afferents
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Exogenous administration of nerve growth factor (NGF) to the bladder or spinal cord induces bladder overactivity in experimental animal models
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NGF—and possibly brain-derived neurotrophic factor (BDNF)—is produced in the bladder by urothelium and smooth muscle cells upon stretch and inflammation to sensitize underlying bladder afferent C fibres
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Peripheral or central NGF sequestration reduces bladder overactivity in experimental models of spinal cord injury, bladder inflammation and outlet obstruction; local NGF delivery improves bladder underactivity in experimental diabetic cystopathy
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NGF and BDNF represent potential disease biomarkers for bladder pain syndrome/interstitial cystitis (BPS/IC) and overactive bladder syndrome; increased urinary excretion correlates with symptom severity and can be modulated by therapy
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Neurotrophin system intervention using the monoclonal NGF antibody tanezumab has been shown to improve self-reported bladder pain scores and urgency episode frequency in patients with BPS/IC
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Acknowledgements
Work in the laboratories of P. Ochodnicky, C. D. Cruz and F. Cruz is supported by the European Community's FP7, HEALTH-F2-2008-223234 InComb grant. Work in the laboratory of N. Yoshimura is supported by the National Institutes of Health (DK057267 and DK088836) and the United States Department of Defense (SC100134 and PR110326). The authors thank Martin C. Michel for his inspiration and help during the preparation of this manuscript.
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P. Ochodnicky researched data for the article. C. Cruz and P. Ochodnicky wrote the article. All authors contributed towards discussions of content, in addition to reviewing and editing the manuscript prior to submission.
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Peter Ochodnicky, Celia Cruz and Naoki Yoshimura declare no competing interests. Francisco Cruz has provided consultancy, received honoraria and research support from Allergan, Astellas, Recordati and received speakers honoraria from AMS and Pfizer.
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Ochodnicky, P., Cruz, C., Yoshimura, N. et al. Neurotrophins as regulators of urinary bladder function. Nat Rev Urol 9, 628–637 (2012). https://doi.org/10.1038/nrurol.2012.178
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DOI: https://doi.org/10.1038/nrurol.2012.178
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