New targets for overactive bladder-ICI-RS 2109.


Journal

Neurourology and urodynamics
ISSN: 1520-6777
Titre abrégé: Neurourol Urodyn
Pays: United States
ID NLM: 8303326

Informations de publication

Date de publication:
07 2020
Historique:
received: 14 09 2019
accepted: 31 10 2019
pubmed: 19 11 2019
medline: 22 12 2020
entrez: 19 11 2019
Statut: ppublish

Résumé

To review evidence for novel drug targets that can manage overactive bladder (OAB) symptoms. A think tank considered evidence from the literature and their own research experience to propose new drug targets in the urinary bladder to characterize their use to treat OAB. Five classes of agents or cellular pathways were considered. (a) Cyclic nucleotide-dependent (cyclic adenosine monophosphate and cyclic guanosine monophosphate) pathways that modulate adenosine triphosphate release from motor nerves and urothelium. (b) Novel targets for β The specificity of action remains a consideration if particular classes of agents can be considered for future development as receptors or pathways that mediate actions of the above mentioned potential agents are distributed among most organ systems. The tasks are to determine more detail of the pathological changes that occur in the OAB and how the specificity of potential drugs may be directed to bladder pathological changes. An important conclusion was that the storage, not the voiding, phase in the micturition cycle should be investigated and potential targets lie in the whole range of tissue in the bladder wall and not just detrusor.

Identifiants

pubmed: 31737931
doi: 10.1002/nau.24228
pmc: PMC8114459
mid: NIHMS1699942
doi:

Substances chimiques

Urological Agents 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

S113-S121

Subventions

Organisme : Medical Research Council
ID : MR/M012425/1
Pays : United Kingdom
Organisme : NIDDK NIH HHS
ID : R01 DK098361
Pays : United States

Informations de copyright

© 2019 Wiley Periodicals, Inc.

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Auteurs

Christopher Henry Fry (CH)

School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, UK.

Basu Chakrabarty (B)

School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, UK.

Hikaru Hashitani (H)

Department of Cell Physiology, Nagoya City University, Nagoya, Japan.

Karl-Erik Andersson (KE)

Institute of Laboratory Medicine, Lund University, Lund, Sweden.
Institute for Regenerative Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina.

Karen McCloskey (K)

School of Medicine, Dentistry and Biomedical Sciences, Queens University Belfast, Belfast, UK.

Rita I Jabr (RI)

Division of Biochemical Sciences, Faculty of Health and Biomedical Sciences, University of Surrey, Guildford, UK.

Marcus J Drake (MJ)

Bristol Medical School, University of Bristol, Bristol, UK.

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Classifications MeSH