Involvement of Large‐Conductance Ca2+‐Activated K+ Channels in both Nitric Oxide and Endothelium‐Derived Hyperpolarization‐Type Relaxation in Human Penile Small Arteries. (21st March 2013)
- Record Type:
- Journal Article
- Title:
- Involvement of Large‐Conductance Ca2+‐Activated K+ Channels in both Nitric Oxide and Endothelium‐Derived Hyperpolarization‐Type Relaxation in Human Penile Small Arteries. (21st March 2013)
- Main Title:
- Involvement of Large‐Conductance Ca2+‐Activated K+ Channels in both Nitric Oxide and Endothelium‐Derived Hyperpolarization‐Type Relaxation in Human Penile Small Arteries
- Authors:
- Király, István
Pataricza, János
Bajory, Zoltán
Simonsen, Ulf
Varro, András
Papp, Julius Gy.
Pajor, Lászlo
Kun, Attila - Abstract:
- <abstract abstract-type="main" xml:lang="en" id="bcpt12059-abs-0001"> <title>Abstract</title> <p>Large‐conductance Ca<sup>2+</sup>‐activated K<sup>+</sup> channels (BK<sub>C</sub><sub>a</sub>), located on the vascular smooth muscle, play an important role in regulation of vascular tone. In penile corpus cavernosum tissue, opening of BK<sub>C</sub><sub>a</sub> channels leads to relaxation of corporal smooth muscle, which is essential during erection; however, there is little information on the role of BK<sub>C</sub><sub>a</sub> channels located in penile vascular smooth muscle. This study was designed to investigate the involvement of BK<sub>C</sub><sub>a</sub> channels in endothelium‐dependent and endothelium‐independent relaxation of human intracavernous penile arteries. In human intracavernous arteries obtained in connection with transsexual operations, change in isometric force was recorded in microvascular myographs, and endothelium‐dependent [nitric oxide (NO) and endothelium‐derived hyperpolarization (EDH)‐type] and endothelium‐independent (NO‐donor) relaxations were measured in contracted arteries. In penile small arteries contracted with phenylephrine, acetylcholine evoked NO‐ and EDH‐type relaxations, which were sensitive to iberiotoxin (IbTX), a selective blocker of BK<sub>C</sub><sub>a</sub> channels. Iberiotoxin also inhibited relaxations induced by a NO‐donor, sodium nitroprusside. NS11021, a selective opener of BK<sub>C</sub><sub>a</sub> channels, evoked<abstract abstract-type="main" xml:lang="en" id="bcpt12059-abs-0001"> <title>Abstract</title> <p>Large‐conductance Ca<sup>2+</sup>‐activated K<sup>+</sup> channels (BK<sub>C</sub><sub>a</sub>), located on the vascular smooth muscle, play an important role in regulation of vascular tone. In penile corpus cavernosum tissue, opening of BK<sub>C</sub><sub>a</sub> channels leads to relaxation of corporal smooth muscle, which is essential during erection; however, there is little information on the role of BK<sub>C</sub><sub>a</sub> channels located in penile vascular smooth muscle. This study was designed to investigate the involvement of BK<sub>C</sub><sub>a</sub> channels in endothelium‐dependent and endothelium‐independent relaxation of human intracavernous penile arteries. In human intracavernous arteries obtained in connection with transsexual operations, change in isometric force was recorded in microvascular myographs, and endothelium‐dependent [nitric oxide (NO) and endothelium‐derived hyperpolarization (EDH)‐type] and endothelium‐independent (NO‐donor) relaxations were measured in contracted arteries. In penile small arteries contracted with phenylephrine, acetylcholine evoked NO‐ and EDH‐type relaxations, which were sensitive to iberiotoxin (IbTX), a selective blocker of BK<sub>C</sub><sub>a</sub> channels. Iberiotoxin also inhibited relaxations induced by a NO‐donor, sodium nitroprusside. NS11021, a selective opener of BK<sub>C</sub><sub>a</sub> channels, evoked pronounced relaxations that were inhibited in the presence of IbTX. NS13558, a BK<sub>C</sub><sub>a</sub>‐inactive analogue of NS11021, failed to relax human penile small arteries. Our results show that BK<sub>C</sub><sub>a</sub> channels are involved in both NO‐ and EDH‐type relaxation of intracavernous penile arteries obtained from healthy men. The effect of a selective opener of BK<sub>C</sub><sub>a</sub> channels also suggests that direct activation of the channel may be an advantageous approach for treatment of impaired endothelium‐dependent relaxation often associated with erectile dysfunction.</p> </abstract> … (more)
- Is Part Of:
- Basic & clinical pharmacology & toxicology. Volume 113:Number 1(2013)
- Journal:
- Basic & clinical pharmacology & toxicology
- Issue:
- Volume 113:Number 1(2013)
- Issue Display:
- Volume 113, Issue 1 (2013)
- Year:
- 2013
- Volume:
- 113
- Issue:
- 1
- Issue Sort Value:
- 2013-0113-0001-0000
- Page Start:
- 19
- Page End:
- 24
- Publication Date:
- 2013-03-21
- Subjects:
- Pharmacology -- Periodicals
Toxicology -- Periodicals
Pharmacology -- Periodicals
Toxicology -- Periodicals
Pharmacology, Clinical -- Periodicals
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Electronic journals
615.1 - Journal URLs:
- http://firstsearch.oclc.org/journal=1742-7835;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1742-7843 ↗
http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=pto ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/bcpt.12059 ↗
- Languages:
- English
- ISSNs:
- 1742-7835
- Deposit Type:
- Legaldeposit
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