β3 Relaxant Effect in Human Bladder Involves Cystathionine γ-Lyase-Derived Urothelial Hydrogen Sulfide

It is now well established that the urothelium does not act as a passive barrier but contributes to bladder homeostasis by releasing several signaling molecules in response to physiological and chemical stimuli. Here, we investigated the potential contribution of the hydrogen sulfide (H2S) pathway in regulating human urothelium function in beta(3) adrenoceptor-mediated relaxation. The relaxant effect of BRL 37344 (0.1-300 mu M), a selective beta(3) adrenoceptor agonist, was evaluated in isolated human bladder strips in the presence or absence of the urothelium. The relaxant effect of BRL 37344 was significantly reduced by urothelium removal. The inhibition of cystathionine-gamma-lyase (CSE), but not cystathionine-beta-synthase (CBS), significantly reduced the BRL 37344 relaxing effect to the same extent as that given by urothelium removal, suggesting a role for CSE-derived H2S. beta(3) adrenoceptor stimulation in the human urothelium or in T24 urothelial cells markedly increased H2S and cAMP levels that were reverted by a blockade of CSE and beta(3) adrenoceptor antagonism. These findings demonstrate a key role for urothelium CSE-derived H2S in the beta(3) effect on the human bladder through the modulation of cAMP levels. Therefore, the study establishes the relevance of urothelial beta(3) adrenoceptors in the regulation of bladder tone, supporting the use of beta(3) agonists in patients affected by an overactive bladder.

Automated summary

The urothelium plays an important role in bladder homeostasis through the hydrogen sulfide pathway and beta(3) adrenoceptor-mediated relaxation. The study demonstrates the relevance of urothelial beta(3) adrenoceptors in regulating bladder tone and supports the use of beta(3) agonists in patients with an overactive bladder.