Study on Physiological Roles of Stimulation of Prostaglandin E2 Receptor Subtype EP2 in Urethral Function in Rats

• Published in: Lower urinary tract symptoms Vol. 8; no. 2; pp. 125 - 129
• Main Authors: KURIHARA, Ryoko, ISHIZU, Kenichiro, TAKAMATSU, Hajime, YOSHINO, Taiji, MASUDA, Noriyuki
• Format: Journal Article
• Language: English
• Published: Australia Blackwell Publishing Asia Pty Ltd 01.05.2016; Wiley Subscription Services, Inc
• Subjects: Analysis of Variance; Animals; cAMP; CHO Cells; Cricetinae; Cricetulus; Cyclic AMP - metabolism; Dose-Response Relationship, Drug; EP2; Female; Male; Muscle Relaxation - drug effects; Pyridines - pharmacology; Rats, Sprague-Dawley; Receptors, Prostaglandin E, EP2 Subtype - agonists; Receptors, Prostaglandin E, EP2 Subtype - physiology; Receptors, Prostaglandin E, EP4 Subtype - metabolism; relaxation; urethra; Urethra - drug effects; Urethra - physiology; cAMP; urethra; EP2; relaxation
• ISSN: 1757-5664; 1757-5672
• DOI: 10.1111/luts.12077

Objectives We investigated the relaxant effect of stimulation of prostaglandin E2 (PGE2) receptor subtype EP2 as well as the involvement of a cyclic AMP (cAMP)‐dependent pathway related to stimulation of EP2 receptors in urethral function in rats by evaluating effects of PGE2 and selective EP2 receptor agonist CP‐533,536. Methods Effects of PGE2 and CP‐533,536 on cAMP accumulation were assessed in Chinese hamster ovary (CHO)‐K1 cells expressing rat EP2 or EP4 receptors. Relaxant responses to PGE2 and CP‐533,536 (0.01–10 µmol/L) in rat urethral tissue pre‐contracted with 10 µmol/L phenylephrine were evaluated, and cAMP levels in isolated rat urethral tissue treated with these compounds were determined as well. The effects of PGE2 and CP‐533,536 (0.003–0.3 mg/kg intravenously) on urethral perfusion pressure (UPP) in anesthetized rats were also evaluated. Results PGE2 concentration‐dependently increased the accumulation of cAMP in cells expressing rat EP2 (EC50 value = 1.3 nmol/L) and EP4 receptors (EC50 value = 17 nmol/L). While CP‐533,536 similarly increased the accumulation of cAMP in cells expressing rat EP2 receptors (EC50 value = 3.0 nmol/L), no such effects were noted in cells expressing rat EP4 receptors up to 10 µmol/L. Both PGE2 and CP‐533,536 produced relaxation and increased cAMP levels in urethral tissues in a concentration‐dependent manner. PGE2 and CP‐533,536 both dose‐dependently decreased UPP in anesthetized rats. Conclusions Taken together, these results suggest that stimulation of EP2 receptors induces relaxation likely via activation of cAMP‐dependent mechanisms in rat urethral tissue, leading to a reduction of UPP.