Effects of Endopeptidase Inhibition on the Contraction–Relaxation Response of Isolated Human Vaginal Tissue. (24th January 2013)
- Record Type:
- Journal Article
- Title:
- Effects of Endopeptidase Inhibition on the Contraction–Relaxation Response of Isolated Human Vaginal Tissue. (24th January 2013)
- Main Title:
- Effects of Endopeptidase Inhibition on the Contraction–Relaxation Response of Isolated Human Vaginal Tissue
- Authors:
- Rahardjo, Harrina E.
Ückert, Stefan
Taher, Akmal
Sonnenberg, Joachim E.
Kauffels, Wolfgang
Rahardjo, Djoko
Kuczyk, Markus A. - Abstract:
- <abstract abstract-type="main"> <title>Abstract</title> <sec id="jsm12064-sec-0001" sec-type="section"> <title>Introduction.</title> <p>Vasoactive peptides, such as bradykinin, C‐type natriuretic peptide (CNP), vasoactive intestinal polypeptide (VIP), and endothelin 1 (ET‐1), are assumed to be involved in the control of female genital vascular and nonvascular smooth muscle. Tissue levels of said peptides are controlled by the activity of endopeptidase enzymes. Theoretically, in female genital tissues, inhibiting the degradation of bradykinin, CNP, and VIP, or the conversion of Big ET‐1 into ET‐1 should result in an enhancement in smooth muscle relaxation and, thus, an improvement in sexual response.</p> </sec> <sec id="jsm12064-sec-0002" sec-type="section"> <title>Aim.</title> <p>Elucidate the effects of the endopeptidase inhibitor KC 12615 on the contraction/relaxation response of isolated human vaginal smooth muscle to Big ET‐1, bradykinin, CNP, or VIP.</p> </sec> <sec id="jsm12064-sec-0003" sec-type="section"> <title>Methods.</title> <p>Tissue bath experiments were carried out to ascertain the responses of human vaginal tissue challenged by ET‐1 (0.1 μM) to increasing concentrations of bradykinin, CNP, and VIP (0.01 μM, 0.1 μM, and 1 μM, respectively). The effects were also evaluated following preexposure to KC 12615 (10 μM, for 20 minutes).</p> </sec> <sec id="jsm12064-sec-0004" sec-type="section"> <title>Main Outcome Measures.</title> <p>Measure the effects of KC 12615<abstract abstract-type="main"> <title>Abstract</title> <sec id="jsm12064-sec-0001" sec-type="section"> <title>Introduction.</title> <p>Vasoactive peptides, such as bradykinin, C‐type natriuretic peptide (CNP), vasoactive intestinal polypeptide (VIP), and endothelin 1 (ET‐1), are assumed to be involved in the control of female genital vascular and nonvascular smooth muscle. Tissue levels of said peptides are controlled by the activity of endopeptidase enzymes. Theoretically, in female genital tissues, inhibiting the degradation of bradykinin, CNP, and VIP, or the conversion of Big ET‐1 into ET‐1 should result in an enhancement in smooth muscle relaxation and, thus, an improvement in sexual response.</p> </sec> <sec id="jsm12064-sec-0002" sec-type="section"> <title>Aim.</title> <p>Elucidate the effects of the endopeptidase inhibitor KC 12615 on the contraction/relaxation response of isolated human vaginal smooth muscle to Big ET‐1, bradykinin, CNP, or VIP.</p> </sec> <sec id="jsm12064-sec-0003" sec-type="section"> <title>Methods.</title> <p>Tissue bath experiments were carried out to ascertain the responses of human vaginal tissue challenged by ET‐1 (0.1 μM) to increasing concentrations of bradykinin, CNP, and VIP (0.01 μM, 0.1 μM, and 1 μM, respectively). The effects were also evaluated following preexposure to KC 12615 (10 μM, for 20 minutes).</p> </sec> <sec id="jsm12064-sec-0004" sec-type="section"> <title>Main Outcome Measures.</title> <p>Measure the effects of KC 12615 on the relaxation of isolated human vaginal smooth muscle brought about by bradykinin, CNP, or VIP and the contraction mediated by Big ET‐1.</p> </sec> <sec id="jsm12064-sec-0005" sec-type="section"> <title>Results.</title> <p>The tension induced by ET‐1 was reversed by bradykinin, CNP, or VIP (−25 ± 6.6%, −13.3 ± 2.2%, and −17.6 ± 10%, respectively). Big ET‐1 induced contraction of the vaginal tissue. Preexposure of the tissue to KC 12615 increased the relaxation exerted by bradykinin, CNP, or VIP (to −39.2 ± 5.8%, −40.7 ± 7.3%, and −44.6 ± 19%, respectively). The contraction induced by Big ET‐1 was attenuated in the presence of KC 12615 (to approximately 25% of the initial response).</p> </sec> <sec id="jsm12064-sec-0006" sec-type="section"> <title>Conclusion.</title> <p>Inhibition of endopeptidase activity can antagonize the contraction of human vaginal tissue induced by Big ET‐1 and increase the relaxation induced by vasoactive endogenous peptides.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of sexual medicine. Volume 10:Number 4(2013:Apr.)
- Journal:
- Journal of sexual medicine
- Issue:
- Volume 10:Number 4(2013:Apr.)
- Issue Display:
- Volume 10, Issue 4 (2013)
- Year:
- 2013
- Volume:
- 10
- Issue:
- 4
- Issue Sort Value:
- 2013-0010-0004-0000
- Page Start:
- 951
- Page End:
- 959
- Publication Date:
- 2013-01-24
- Subjects:
- Sexual disorders -- Periodicals
Sex -- Periodicals
Sexual health -- Periodicals
616.69005 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1743-6109 ↗
http://www.blackwell-synergy.com/openurl?genre=journal&eissn=1743-6109 ↗
http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=jsm ↗
https://academic.oup.com/jsm ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/jsm.12064 ↗
- Languages:
- English
- ISSNs:
- 1743-6095
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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