028 Hydrogen Sulfide has a Role as an Endogenous Relaxation Factor in the Rat Prostate. (1st May 2022)

• Record Type: Journal Article
• Authors: Shimizu, T.; Zou, S.; Shimizu, S.; Aratake, T.; Higashi, Y.; Yamamoto, M.; Saito, M.
• Is Part Of: Journal of sexual medicine. Volume 19(2022)Supplement 2
• Page Start: S136
• Page End: S136
• Publication Date: 2022-05-01
• Subjects: Sexual disorders -- Periodicals; Sex -- Periodicals; Sexual health -- Periodicals; 616.69005
• DOI: 10.1016/j.jsxm.2022.03.564
• Languages: English
• ISSNs: 1743-6095

Abstract

ABSTRACT: Introduction: Hydrogen sulfide (H2 S) is the third endogenous gasotransmitter besides carbon monoxide and nitric oxide, and has a wide range of physiological functions such as neuromodulation, vasorelaxation and cytoprotection. Although in human prostate cancer cells, NaHS (a H2 S donor) treatment was reported to inhibit proliferation and to elevate secretory function, physiological functions of H2 S in the prostate tissue had not been investigated yet. Endogenous H2 S is biosynthesized from L-cysteine by cystathionine β-synthase (CBS) and cystathionine γ-lyase (CSE). In addition, 3-mercaptopyruvate sulfurtransferase (MPST) synthesizes H2 S from 3-mercaptopyruvate (3MP), which is produced from L-cysteine by cysteine aminotransferase (CAT) (CAT/MPST pathway). Recently, a new pathway for endogenous H2 S biosynthesis is reported; D-cysteine is metabolized by D-amino acid oxidase (DAO) to 3MP, which is a substrate for MPST to synthesize H2 S. Objective: We investigated (1) tissue distribution of CBS, CSE, MPST, CAT and DAO, (2) endogenous H2 S levels, and (3) effects of NaHS on contractility in the rat prostate. Methods: Dorsolateral and ventral prostate (PR-D and PR-V), liver and cerebellum (L and C) were prepared from male Wistar rats (300-400 g) sacrificed with an overdose of sodium pentobarbital (80 mg/kg, ip). (1) Tissue distributions of 5 enzymes were investigated by real-time PCR, western blot and immunohistochemistry. L and C were used for positive controls. (2) H2 S contents in the prostate tissues were measured by methylene blue method. (3) By using 1 x 5 mm strips of the prostate tissues, effects of NaHS (1 x 10 -9 to 3 x 10 -4 M) were evaluated on pre-contracted prostate strips by noradrenaline (10 -5 M). Prostate strips were pretreated with propranolol (10 -6 M) 30 min before the pre-contraction. Results: (1) CBS, MPST and CAT were detected in the prostate. Expression levels of CBS in the PR-D were lower than those in the PR-V, and the levels of MPST in the PR-D were higher than those in the PR-V. In expression levels of CAT, there was no significant difference between two prostate tissues. On the other hand, CSE or DAO was not detected in these tissues. Immunoreactvities of these enzymes were mainly detected in the prostate glandular epithelium. (2) H2 S was detected in the prostate tissues. (3) NaHS dose-dependently induced relaxation of pre-contracted PR-D and PR-V strips. There were no significant differences of the EC50 values or relaxation rate against the pre-contractions between two prostate tissues. Conclusion: H2 S synthesized by CBS- and CAT/MPST-mediated pathways has a role as an endogenous relaxation factor in the rat prostate. Therefore, endogenous H2 S might open new avenues of therapeutic interventions for benign prostatic hyperplasia. Disclosure: Work supported by industry: no.