A Toll‐Like Receptor 1/2 Agonist Augments Contractility in Rat Corpus Cavernosum
Activation of the innate immune Toll‐like receptor 2 (TLR2) initiates inflammation and has been implicated in vascular dysfunction. Increased contraction and decreased relaxation responses in the penile vasculature lead to erectile dysfunction, a condition associated with inflammation. However, whet...
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Veröffentlicht in: | Journal of sexual medicine 2015-08, Vol.12 (8), p.1722-1731 |
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creator | Stallmann‐Jorgensen, Inger Ogbi, Safia Szasz, Theodora Webb, R. Clinton |
description | Activation of the innate immune Toll‐like receptor 2 (TLR2) initiates inflammation and has been implicated in vascular dysfunction. Increased contraction and decreased relaxation responses in the penile vasculature lead to erectile dysfunction, a condition associated with inflammation. However, whether TLR2 activation plays a role in penile vascular function has not been established.
We hypothesized that activation of the TLR 1/2 heterodimer (TLR1/2) augments contractile and impairs relaxation responses of corpus cavernosum and that these perturbations of vascular function are mediated by low nitric oxide (NO) availability and enhanced activity of the RhoA/Rho‐kinase pathway.
Contraction and relaxation responses were measured in rat cavernosal strips using a myograph after incubation with a TLR1/2‐activating ligand Pam3CSK4 (Pam3), the TLR1/2 inhibitor CuCPT 22 (CuCPT), and inhibitors of NO synthase (LNAME) and Rho‐kinase (Y27632). TLR2 protein expression was assessed by immunohistochemistry.
Cumulative concentration response curves, sensitivity (pEC50), and maximal response (Emax) of cavernosal strips to vasodilatory and vasocontractile agonists were compared between treatments.
Pam3‐treated cavernosal strips exhibited greater pEC50 and higher Emax to phenylephrine (PE) than control tissues. Inhibition of NO synthase increased Emax to PE in Pam3‐treated cavernosal strips. Pam3 treatment reduced relaxation to Y27632 compared with control tissues. Inhibition of TLR1/2 activation with CuCPT returned the augmented contraction to PE and the decreased relaxation to Y27632 of Pam3‐treated cavernosal strips to control values.
The TLR1/2 heterodimer mediates augmented contraction and reduced relaxation in rat cavernosal strips. Thus, TLR1/2 activation antagonizes vascular responses crucial for normal erectile function and implicates immune activation in vasculogenic erectile dysfunction. Immune signaling via TLR2 may offer novel targets for treating inflammation‐mediated vascular dysfunction in the penis. Stallmann‐Jorgensen I, Ogbi S, Szasz T, and Webb RC. A Toll‐like receptor 1/2 agonist augments contractility in rat corpus cavernosum. J Sex Med 2015;12:1722–1731. |
doi_str_mv | 10.1111/jsm.12960 |
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We hypothesized that activation of the TLR 1/2 heterodimer (TLR1/2) augments contractile and impairs relaxation responses of corpus cavernosum and that these perturbations of vascular function are mediated by low nitric oxide (NO) availability and enhanced activity of the RhoA/Rho‐kinase pathway.
Contraction and relaxation responses were measured in rat cavernosal strips using a myograph after incubation with a TLR1/2‐activating ligand Pam3CSK4 (Pam3), the TLR1/2 inhibitor CuCPT 22 (CuCPT), and inhibitors of NO synthase (LNAME) and Rho‐kinase (Y27632). TLR2 protein expression was assessed by immunohistochemistry.
Cumulative concentration response curves, sensitivity (pEC50), and maximal response (Emax) of cavernosal strips to vasodilatory and vasocontractile agonists were compared between treatments.
Pam3‐treated cavernosal strips exhibited greater pEC50 and higher Emax to phenylephrine (PE) than control tissues. Inhibition of NO synthase increased Emax to PE in Pam3‐treated cavernosal strips. Pam3 treatment reduced relaxation to Y27632 compared with control tissues. Inhibition of TLR1/2 activation with CuCPT returned the augmented contraction to PE and the decreased relaxation to Y27632 of Pam3‐treated cavernosal strips to control values.
The TLR1/2 heterodimer mediates augmented contraction and reduced relaxation in rat cavernosal strips. Thus, TLR1/2 activation antagonizes vascular responses crucial for normal erectile function and implicates immune activation in vasculogenic erectile dysfunction. Immune signaling via TLR2 may offer novel targets for treating inflammation‐mediated vascular dysfunction in the penis. Stallmann‐Jorgensen I, Ogbi S, Szasz T, and Webb RC. A Toll‐like receptor 1/2 agonist augments contractility in rat corpus cavernosum. J Sex Med 2015;12:1722–1731.</description><identifier>ISSN: 1743-6095</identifier><identifier>EISSN: 1743-6109</identifier><identifier>DOI: 10.1111/jsm.12960</identifier><identifier>PMID: 26234560</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Animals ; Corpus Cavernosum ; Disease Models, Animal ; Endothelium, Vascular - metabolism ; Erectile Dysfunction - pathology ; Erectile Dysfunction - physiopathology ; Erectile Function ; Humans ; Male ; Muscle Contraction - drug effects ; Muscle Contraction - physiology ; Myography ; Nitric Oxide ; Nitric Oxide - metabolism ; Penile Erection - drug effects ; Penile Erection - physiology ; Penis - blood supply ; Penis - innervation ; Penis - pathology ; Rats ; rho-Associated Kinases - metabolism ; Rho‐Kinase ; Toll-Like Receptor 1 ; Toll-Like Receptor 2 ; Vascular Dysfunction</subject><ispartof>Journal of sexual medicine, 2015-08, Vol.12 (8), p.1722-1731</ispartof><rights>2015 International Society for Sexual Medicine</rights><rights>2015 International Society for Sexual Medicine.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3690-f749379c668690b9245eb2b7abd0b144422142bb83013bdf7d50380f77c398e93</citedby><cites>FETCH-LOGICAL-c3690-f749379c668690b9245eb2b7abd0b144422142bb83013bdf7d50380f77c398e93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjsm.12960$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjsm.12960$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26234560$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stallmann‐Jorgensen, Inger</creatorcontrib><creatorcontrib>Ogbi, Safia</creatorcontrib><creatorcontrib>Szasz, Theodora</creatorcontrib><creatorcontrib>Webb, R. Clinton</creatorcontrib><title>A Toll‐Like Receptor 1/2 Agonist Augments Contractility in Rat Corpus Cavernosum</title><title>Journal of sexual medicine</title><addtitle>J Sex Med</addtitle><description>Activation of the innate immune Toll‐like receptor 2 (TLR2) initiates inflammation and has been implicated in vascular dysfunction. Increased contraction and decreased relaxation responses in the penile vasculature lead to erectile dysfunction, a condition associated with inflammation. However, whether TLR2 activation plays a role in penile vascular function has not been established.
We hypothesized that activation of the TLR 1/2 heterodimer (TLR1/2) augments contractile and impairs relaxation responses of corpus cavernosum and that these perturbations of vascular function are mediated by low nitric oxide (NO) availability and enhanced activity of the RhoA/Rho‐kinase pathway.
Contraction and relaxation responses were measured in rat cavernosal strips using a myograph after incubation with a TLR1/2‐activating ligand Pam3CSK4 (Pam3), the TLR1/2 inhibitor CuCPT 22 (CuCPT), and inhibitors of NO synthase (LNAME) and Rho‐kinase (Y27632). TLR2 protein expression was assessed by immunohistochemistry.
Cumulative concentration response curves, sensitivity (pEC50), and maximal response (Emax) of cavernosal strips to vasodilatory and vasocontractile agonists were compared between treatments.
Pam3‐treated cavernosal strips exhibited greater pEC50 and higher Emax to phenylephrine (PE) than control tissues. Inhibition of NO synthase increased Emax to PE in Pam3‐treated cavernosal strips. Pam3 treatment reduced relaxation to Y27632 compared with control tissues. Inhibition of TLR1/2 activation with CuCPT returned the augmented contraction to PE and the decreased relaxation to Y27632 of Pam3‐treated cavernosal strips to control values.
The TLR1/2 heterodimer mediates augmented contraction and reduced relaxation in rat cavernosal strips. Thus, TLR1/2 activation antagonizes vascular responses crucial for normal erectile function and implicates immune activation in vasculogenic erectile dysfunction. Immune signaling via TLR2 may offer novel targets for treating inflammation‐mediated vascular dysfunction in the penis. Stallmann‐Jorgensen I, Ogbi S, Szasz T, and Webb RC. A Toll‐like receptor 1/2 agonist augments contractility in rat corpus cavernosum. J Sex Med 2015;12:1722–1731.</description><subject>Animals</subject><subject>Corpus Cavernosum</subject><subject>Disease Models, Animal</subject><subject>Endothelium, Vascular - metabolism</subject><subject>Erectile Dysfunction - pathology</subject><subject>Erectile Dysfunction - physiopathology</subject><subject>Erectile Function</subject><subject>Humans</subject><subject>Male</subject><subject>Muscle Contraction - drug effects</subject><subject>Muscle Contraction - physiology</subject><subject>Myography</subject><subject>Nitric Oxide</subject><subject>Nitric Oxide - metabolism</subject><subject>Penile Erection - drug effects</subject><subject>Penile Erection - physiology</subject><subject>Penis - blood supply</subject><subject>Penis - innervation</subject><subject>Penis - pathology</subject><subject>Rats</subject><subject>rho-Associated Kinases - metabolism</subject><subject>Rho‐Kinase</subject><subject>Toll-Like Receptor 1</subject><subject>Toll-Like Receptor 2</subject><subject>Vascular Dysfunction</subject><issn>1743-6095</issn><issn>1743-6109</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEtOwzAQhi0E4r3gAihLWLT1I4njZVXxVBFSgbUVO5PKkMTFdkDdcQTOyEkwlLKC2Yw9_uaX9SF0RPCQxBo9-nZIqMjxBtolPGWDnGCxuT5jke2gPe8fMWax6DbaoTllaZbjXTQbJ_e2aT7e3qfmCZIZaFgE6xIyosl4bjvjQzLu5y10wScT2wVX6mAaE5aJ6ZJZGeLQLfr4Vr6A66zv2wO0VZeNh8Ofvo8ezs_uJ5eD6e3F1WQ8HWiWCzyoeSoYFzrPi3hVgqYZKKp4qSqsSJqmlJKUKlUwTJiqal5lmBW45lwzUYBg--hklbtw9rkHH2RrvIamKTuwvZeE44wzVnAe0dMVqp313kEtF860pVtKguWXQhkVym-FkT3-ie1VC9UvuXYWgdEKeDUNLP9Pktd3N-tIttqAqOPFgJNeG-g0VMaBDrKy5o-PfAImM4tN</recordid><startdate>201508</startdate><enddate>201508</enddate><creator>Stallmann‐Jorgensen, Inger</creator><creator>Ogbi, Safia</creator><creator>Szasz, Theodora</creator><creator>Webb, R. Clinton</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201508</creationdate><title>A Toll‐Like Receptor 1/2 Agonist Augments Contractility in Rat Corpus Cavernosum</title><author>Stallmann‐Jorgensen, Inger ; Ogbi, Safia ; Szasz, Theodora ; Webb, R. Clinton</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3690-f749379c668690b9245eb2b7abd0b144422142bb83013bdf7d50380f77c398e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Corpus Cavernosum</topic><topic>Disease Models, Animal</topic><topic>Endothelium, Vascular - metabolism</topic><topic>Erectile Dysfunction - pathology</topic><topic>Erectile Dysfunction - physiopathology</topic><topic>Erectile Function</topic><topic>Humans</topic><topic>Male</topic><topic>Muscle Contraction - drug effects</topic><topic>Muscle Contraction - physiology</topic><topic>Myography</topic><topic>Nitric Oxide</topic><topic>Nitric Oxide - metabolism</topic><topic>Penile Erection - drug effects</topic><topic>Penile Erection - physiology</topic><topic>Penis - blood supply</topic><topic>Penis - innervation</topic><topic>Penis - pathology</topic><topic>Rats</topic><topic>rho-Associated Kinases - metabolism</topic><topic>Rho‐Kinase</topic><topic>Toll-Like Receptor 1</topic><topic>Toll-Like Receptor 2</topic><topic>Vascular Dysfunction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stallmann‐Jorgensen, Inger</creatorcontrib><creatorcontrib>Ogbi, Safia</creatorcontrib><creatorcontrib>Szasz, Theodora</creatorcontrib><creatorcontrib>Webb, R. Clinton</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of sexual medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stallmann‐Jorgensen, Inger</au><au>Ogbi, Safia</au><au>Szasz, Theodora</au><au>Webb, R. Clinton</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Toll‐Like Receptor 1/2 Agonist Augments Contractility in Rat Corpus Cavernosum</atitle><jtitle>Journal of sexual medicine</jtitle><addtitle>J Sex Med</addtitle><date>2015-08</date><risdate>2015</risdate><volume>12</volume><issue>8</issue><spage>1722</spage><epage>1731</epage><pages>1722-1731</pages><issn>1743-6095</issn><eissn>1743-6109</eissn><abstract>Activation of the innate immune Toll‐like receptor 2 (TLR2) initiates inflammation and has been implicated in vascular dysfunction. Increased contraction and decreased relaxation responses in the penile vasculature lead to erectile dysfunction, a condition associated with inflammation. However, whether TLR2 activation plays a role in penile vascular function has not been established.
We hypothesized that activation of the TLR 1/2 heterodimer (TLR1/2) augments contractile and impairs relaxation responses of corpus cavernosum and that these perturbations of vascular function are mediated by low nitric oxide (NO) availability and enhanced activity of the RhoA/Rho‐kinase pathway.
Contraction and relaxation responses were measured in rat cavernosal strips using a myograph after incubation with a TLR1/2‐activating ligand Pam3CSK4 (Pam3), the TLR1/2 inhibitor CuCPT 22 (CuCPT), and inhibitors of NO synthase (LNAME) and Rho‐kinase (Y27632). TLR2 protein expression was assessed by immunohistochemistry.
Cumulative concentration response curves, sensitivity (pEC50), and maximal response (Emax) of cavernosal strips to vasodilatory and vasocontractile agonists were compared between treatments.
Pam3‐treated cavernosal strips exhibited greater pEC50 and higher Emax to phenylephrine (PE) than control tissues. Inhibition of NO synthase increased Emax to PE in Pam3‐treated cavernosal strips. Pam3 treatment reduced relaxation to Y27632 compared with control tissues. Inhibition of TLR1/2 activation with CuCPT returned the augmented contraction to PE and the decreased relaxation to Y27632 of Pam3‐treated cavernosal strips to control values.
The TLR1/2 heterodimer mediates augmented contraction and reduced relaxation in rat cavernosal strips. Thus, TLR1/2 activation antagonizes vascular responses crucial for normal erectile function and implicates immune activation in vasculogenic erectile dysfunction. Immune signaling via TLR2 may offer novel targets for treating inflammation‐mediated vascular dysfunction in the penis. Stallmann‐Jorgensen I, Ogbi S, Szasz T, and Webb RC. A Toll‐like receptor 1/2 agonist augments contractility in rat corpus cavernosum. J Sex Med 2015;12:1722–1731.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>26234560</pmid><doi>10.1111/jsm.12960</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Corpus Cavernosum Disease Models, Animal Endothelium, Vascular - metabolism Erectile Dysfunction - pathology Erectile Dysfunction - physiopathology Erectile Function Humans Male Muscle Contraction - drug effects Muscle Contraction - physiology Myography Nitric Oxide Nitric Oxide - metabolism Penile Erection - drug effects Penile Erection - physiology Penis - blood supply Penis - innervation Penis - pathology Rats rho-Associated Kinases - metabolism Rho‐Kinase Toll-Like Receptor 1 Toll-Like Receptor 2 Vascular Dysfunction |
title | A Toll‐Like Receptor 1/2 Agonist Augments Contractility in Rat Corpus Cavernosum |
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