Hydrogen sulfide as a mediator of human corpus cavernosum smooth-muscle relaxation

Bianca, R.D.D. and Sorrentino, R. and Maffia, Pasquale and Mirone, V. and Imbimbo, C. and Fusco, F. and De Palma, R. and Ignarro, L.J. (2009) Hydrogen sulfide as a mediator of human corpus cavernosum smooth-muscle relaxation. Proceedings of the National Academy of Sciences, 106 (11). pp. 4513-4518. ISSN 0027-8424

Full text not available in this repository.Request a copy from the Strathclyde author

Abstract

Hydrogen sulfide (H2S) is synthesized by 2 enzymes, cystathionine beta-synthase (CBS) and cystathionine gamma-lyase (CSE). L-Cysteine (L-Cys) acts as a natural substrate for the synthesis of H2S. Human penile tissue possesses both CBS and CSE, and tissue homogenates efficiently convert L-Cys to H2S. CBS and CSE are localized in the muscular trabeculae and the smooth-muscle component of the penile artery, whereas CSE but not CBS is also expressed in peripheral nerves. Exogenous H2S [sodium hydrogen sulfide (NaHS)] or L-Cys causes a concentration-dependent relaxation of strips of human corpus cavernosum. L-Cys relaxation is inhibited by the CBS inhibitor, aminoxyacetic acid (AOAA). Electrical field stimulation of human penile tissue, under resting conditions, causes an increase in tension that is significantly potentiated by either propargylglycine (PAG; CSE inhibitor) or AOAA. In rats, NaHS and L-Cys promote penile erection, and the response to L-Cys is blocked by PAG. Our data demonstrate that the L-Cys/H2S pathway mediates human corpus cavernosum smooth-muscle relaxation.