Treatment of the overactive bladder: possible central nervous system drug targets.
(2002) In Urology 59(5 Suppl 1). p.18-24- Abstract
- The well-known side effects of antimuscarinic drugs have focused interest on other modalities of treatment of the overactive bladder. To effectively control bladder activity, identification of suitable targets for pharmacologic intervention is necessary. Such targets may be found in the central nervous system (CNS) or peripherally. Several CNS transmitters may modulate voiding, but few drugs with a defined CNS site of action have been developed for treatment of voiding disorders. Drugs affecting gamma-aminobutyric acid, opioid, serotonin, noradrenaline, dopamine, or glutamatergic receptors and mechanisms are known to influence micturition, and potentially such drugs could be developed for clinical use. However, a selective action on the... (More)
- The well-known side effects of antimuscarinic drugs have focused interest on other modalities of treatment of the overactive bladder. To effectively control bladder activity, identification of suitable targets for pharmacologic intervention is necessary. Such targets may be found in the central nervous system (CNS) or peripherally. Several CNS transmitters may modulate voiding, but few drugs with a defined CNS site of action have been developed for treatment of voiding disorders. Drugs affecting gamma-aminobutyric acid, opioid, serotonin, noradrenaline, dopamine, or glutamatergic receptors and mechanisms are known to influence micturition, and potentially such drugs could be developed for clinical use. However, a selective action on the lower urinary tract may be difficult to obtain. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/108195
- author
- Andersson, Karl-Erik LU
- organization
- publishing date
- 2002
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Bladder Diseases : physiopathology, Bladder Diseases : drug therapy, Dopamine : physiology, Human, Muscarinic Antagonists : therapeutic use, Norepinephrine : physiology, Support, Serotonin : physiology, Non-U.S. Gov't, gamma-Aminobutyric Acid : physiology
- in
- Urology
- volume
- 59
- issue
- 5 Suppl 1
- pages
- 18 - 24
- publisher
- Elsevier
- external identifiers
-
- wos:000175489900004
- pmid:12007518
- scopus:0036234254
- ISSN
- 1527-9995
- DOI
- 10.1016/S0090-4295(01)01634-X
- language
- English
- LU publication?
- yes
- id
- 9287ff12-51a2-4e7a-af6f-fd3ec59df315 (old id 108195)
- alternative location
- http://www.ncbi.nlm.nih.gov:80/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12007518&dopt=Abstract
- date added to LUP
- 2016-04-01 11:48:21
- date last changed
- 2022-01-26 18:30:12
@article{9287ff12-51a2-4e7a-af6f-fd3ec59df315, abstract = {{The well-known side effects of antimuscarinic drugs have focused interest on other modalities of treatment of the overactive bladder. To effectively control bladder activity, identification of suitable targets for pharmacologic intervention is necessary. Such targets may be found in the central nervous system (CNS) or peripherally. Several CNS transmitters may modulate voiding, but few drugs with a defined CNS site of action have been developed for treatment of voiding disorders. Drugs affecting gamma-aminobutyric acid, opioid, serotonin, noradrenaline, dopamine, or glutamatergic receptors and mechanisms are known to influence micturition, and potentially such drugs could be developed for clinical use. However, a selective action on the lower urinary tract may be difficult to obtain.}}, author = {{Andersson, Karl-Erik}}, issn = {{1527-9995}}, keywords = {{Bladder Diseases : physiopathology; Bladder Diseases : drug therapy; Dopamine : physiology; Human; Muscarinic Antagonists : therapeutic use; Norepinephrine : physiology; Support; Serotonin : physiology; Non-U.S. Gov't; gamma-Aminobutyric Acid : physiology}}, language = {{eng}}, number = {{5 Suppl 1}}, pages = {{18--24}}, publisher = {{Elsevier}}, series = {{Urology}}, title = {{Treatment of the overactive bladder: possible central nervous system drug targets.}}, url = {{http://dx.doi.org/10.1016/S0090-4295(01)01634-X}}, doi = {{10.1016/S0090-4295(01)01634-X}}, volume = {{59}}, year = {{2002}}, }