Hydrochlorothiazide Potentiates Contractile Activity of Mouse Cavernosal Smooth Muscle

• Published in: Sexual medicine Vol. 4; no. 2; pp. e115 - e125
• Main Authors: Gagliano-Jucá, Thiago, Napolitano, Mauro, Del Grossi Ferraz Carvalho, Fernanda, Campos, Rafael, Mónica, Fabíola Zakia, Claudino, Mário Angelo, Antunes, Edson, Lopes, Anibal Gil, De Nucci, Gilberto
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.06.2016; Elsevier; Oxford University Press
• Subjects: Adrenergic Mechanism; Corpus Cavernosum; Diuretics; Erectile Dysfunction; Original Research; Erectile Dysfunction; Diuretics; Adrenergic Mechanism; Corpus Cavernosum
• ISSN: 2050-1161; 2050-1161
• DOI: 10.1016/j.esxm.2016.02.003

Hydrochlorothiazide has a negative influence on penile erection but little is known about the mechanism(s) involved. To characterize the effects of this diuretic on mouse corpus cavernosum (CC) smooth muscle in vitro and ex vivo. CC strips of C57BL/6 mice (12–16 weeks old) were mounted in organ baths containing Krebs-Henseleit solution and tissue reactivity was evaluated. Expression of genes encoding diuretic targets and enzymes involved in penile erection were evaluated by polymerase chain reaction. Stimulation-response curves to phenylephrine (10 nmol/L–100 μmol/L) or to electrical field stimulation (1–32 Hz) were constructed, with or without hydrochlorothiazide. Strips of CC from mice after long-term hydrochlorothiazide treatment (6 mg/kg/day for 4 weeks) with or without amiloride (0.6 mg/kg/day for 4 weeks) in vivo also were studied. Nitric oxide and Rho-kinase pathways were evaluated. Hydrochlorothiazide (100 μmol/L) increased the maximum response to phenylephrine by 64% in vitro. This effect was unaffected by the addition of indomethacin (5 μmol/L) but was abolished by N(ω)-nitro-L-arginine methyl ester (100 μmol/L). Hydrochlorothiazide (100 μmol/L) potentiated electrical field stimulation-induced contraction in vitro, but not ex vivo. Long-term treatment with hydrochlorothiazide increased the maximum response to phenylephrine by 60% and resulted in a plasma concentration of 500 ± 180 nmol/L. Amiloride (100μmol/L) caused rightward shifts in concentration-response curves to phenylephrine in vitro. Long-term treatment with hydrochlorothiazide plus amiloride did not significantly increase the maximum response to phenylephrine (+13%). Reverse transcriptase polymerase chain reaction did not detect the NaCl cotransporter in mouse CC. Hydrochlorothiazide did not change Rho-kinase activity, whereas amiloride decreased it in vitro and ex vivo (approximately 18% and 24% respectively). A 40% decrease in Rock1 expression also was observed after long-term treatment with hydrochlorothiazide plus amiloride. Hydrochlorothiazide potentiates contraction of smooth muscle from mouse CC. These findings could explain why diuretics such as hydrochlorothiazide are associated with erectile dysfunction.