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Hydrogen sulfide as a mediator of human corpus cavernosum smooth-muscle relaxation
Author(s) -
Roberta d’Emmanuele di Villa Bianca,
Raffaella Sorrentino,
Pasquale Maffia,
Vincenzo Mirone,
Ciro Imbimbo,
Ferdinando Fusco,
Raffaele De Palma,
Louis J. Ignarro,
Giuseppe Cirino
Publication year - 2009
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0807974105
Subject(s) - cysteine , hydrogen sulfide , chemistry , aminooxyacetic acid , cystathionine beta synthase , stimulation , biochemistry , cystathionine gamma lyase , enzyme , relaxation (psychology) , endocrinology , medicine , biophysics , biology , sulfur , organic chemistry
Hydrogen sulfide (H(2)S) 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 H(2)S. Human penile tissue possesses both CBS and CSE, and tissue homogenates efficiently convert L-Cys to H(2)S. 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 H(2)S [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/H(2)S pathway mediates human corpus cavernosum smooth-muscle relaxation.

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