Diabetes attenuates urothelial modulation of detrusor contractility and spontaneous activity. (20th May 2014)
- Record Type:
- Journal Article
- Title:
- Diabetes attenuates urothelial modulation of detrusor contractility and spontaneous activity. (20th May 2014)
- Main Title:
- Diabetes attenuates urothelial modulation of detrusor contractility and spontaneous activity
- Authors:
- Wang, Yi
Tar, Moses T
Fu, Shibo
Melman, Arnold
Davies, Kelvin P - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="iju12491-sec-0001" sec-type="section"> <title>Objectives</title> <p>To investigate the effect of diabetes on urothelial modulation of bladder contractility.</p> </sec> <sec id="iju12491-sec-0002" sec-type="section"> <title>Methods</title> <p>Bladder strips (urothelium intact or denuded) were prepared from 8‐week‐old streptozotocin‐induced diabetic (<italic>n</italic> = 19) and non‐diabetic control rats (<italic>n</italic> = 10). The effect of modulators of MaxiK (iberiotoxin and tetraethylammonium) and Kv7 (XE991 and retigabine) potassium channel activity were investigated for their effects on both carbachol‐induced force generation and spontaneous contractile activity.</p> </sec> <sec id="iju12491-sec-0003" sec-type="section"> <title>Results</title> <p>In bladder strips from non‐diabetic animals, the presence of the urothelium resulted in marked sensitivity to carbachol‐induced force generation by modulators of MaxiK and Kv7 channel activity, whereas in the diabetic animal urothelial sensitivity to these agents was significantly diminished. Urothelial‐intact bladder strips from non‐diabetic animals were more sensitive to modulators of Kv7 activity in reducing the amplitude of spontaneous phasic contractions than urothelial‐denuded bladder strips, whereas in diabetic animals the presence or absence of the urothelium did not alter the sensitivity to modulators of Kv7 activity.<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="iju12491-sec-0001" sec-type="section"> <title>Objectives</title> <p>To investigate the effect of diabetes on urothelial modulation of bladder contractility.</p> </sec> <sec id="iju12491-sec-0002" sec-type="section"> <title>Methods</title> <p>Bladder strips (urothelium intact or denuded) were prepared from 8‐week‐old streptozotocin‐induced diabetic (<italic>n</italic> = 19) and non‐diabetic control rats (<italic>n</italic> = 10). The effect of modulators of MaxiK (iberiotoxin and tetraethylammonium) and Kv7 (XE991 and retigabine) potassium channel activity were investigated for their effects on both carbachol‐induced force generation and spontaneous contractile activity.</p> </sec> <sec id="iju12491-sec-0003" sec-type="section"> <title>Results</title> <p>In bladder strips from non‐diabetic animals, the presence of the urothelium resulted in marked sensitivity to carbachol‐induced force generation by modulators of MaxiK and Kv7 channel activity, whereas in the diabetic animal urothelial sensitivity to these agents was significantly diminished. Urothelial‐intact bladder strips from non‐diabetic animals were more sensitive to modulators of Kv7 activity in reducing the amplitude of spontaneous phasic contractions than urothelial‐denuded bladder strips, whereas in diabetic animals the presence or absence of the urothelium did not alter the sensitivity to modulators of Kv7 activity. Spontaneous activity in the presence of tetraethylammonium was not affected by the urothelium in bladder strips from either diabetic or non‐diabetic animals.</p> </sec> <sec id="iju12491-sec-0004" sec-type="section"> <title>Conclusions</title> <p>The presence of the urothelium in bladders from non‐diabetic animals modulates the activity of potassium blockers to affect bladder contractility, whereas in the diabetic bladder this effect is attenuated. These findings could help to explain the lack of success of pharmaceutical treatments targeting potassium channels to treat bladder pathology in patients with diseases imparing urothelial function.</p> </sec> </abstract> … (more)
- Is Part Of:
- International journal of urology. Volume 21:Number 10(2014)
- Journal:
- International journal of urology
- Issue:
- Volume 21:Number 10(2014)
- Issue Display:
- Volume 21, Issue 10 (2014)
- Year:
- 2014
- Volume:
- 21
- Issue:
- 10
- Issue Sort Value:
- 2014-0021-0010-0000
- Page Start:
- 1059
- Page End:
- 1064
- Publication Date:
- 2014-05-20
- Subjects:
- Urology -- Periodicals
Genitourinary organs -- Periodicals
Urologic Diseases -- Periodicals
616.6005 - Journal URLs:
- http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=iju ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/iju.12491 ↗
- Languages:
- English
- ISSNs:
- 0919-8172
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4542.697100
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3559.xml