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
Hauptverfasser: Stallmann‐Jorgensen, Inger, Ogbi, Safia, Szasz, Theodora, Webb, R. Clinton
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container_end_page 1731
container_issue 8
container_start_page 1722
container_title Journal of sexual medicine
container_volume 12
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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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. 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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. 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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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