Unit of Endocrinology, Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Unit of Endocrinology, Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy; International PhD School in Clinical and Experimental Medicine (CEM), University of Modena and Reggio Emilia, Modena, Italy.
Mol Cell Endocrinol. 2022 Feb 15;542:111527. doi: 10.1016/j.mce.2021.111527. Epub 2021 Dec 4.
Type 5 phosphodiesterase (PDE5) blockade by inhibitors (PDE5i) results in intracellular cyclic guanosine monophosphate (cGMP) increase and smooth muscle relaxation and are used for the treatment of men erectile dysfunction. Although they have high specificity for PDE5, these inhibitors are suspected to cross-interact also with cyclic adenosine monophosphate (cAMP)-specific PDEs, inducing the intracellular accumulation of this cyclic nucleotide and related testosterone increase, positively impacting male reproductive parameters. However, the link between the use of PDE5i and the activation of cAMP-mediated steroidogenesis is still unclear. We have investigated whether three PDE5i, sildenafil, tadalafil and vardenafil, cross-interacts with the high affinity cAMP-specific enzymes type 8A and 8B PDEs (PDE8A and PDE8B), in live, transfected mouse Leydig tumor (mLTC1) and human embryonic kidney (HEK293) cell lines in vitro. The PDE5i-induced production of cAMP-dependent testosterone and its precursor progesterone was evaluated as well. We have developed PDE8A/B biosensors and modified cyclic nucleotides confirming enzyme binding to cAMP, but not to cGMP, in our cell models. cAMP binding to PDE8A/B was displaced upon cell treatment with PDE5i, revealing that sildenafil, tadalafil and vardenafil have similar effectiveness in live cells, in vitro. The cross-interaction between PDE5i and PDE8A/B supports the gonadotropin-enhanced intracellular cAMP increase, occurring together with cGMP increase, as well as steroid synthesis. Indeed, we found that Leydig cell treatment by PDE5i increases progesterone and testosterone production triggered by gonadotropins. We demonstrated that PDE5i may interact with the cAMP-specific PDE8A and PDE8B, possibly inducing intracellular cAMP and sex steroid hormone increase. These findings support clinical data suggesting that PDE5i might increase testosterone levels in men.
5 型磷酸二酯酶 (PDE5) 抑制剂的阻断作用导致细胞内环鸟苷酸单磷酸 (cGMP) 增加和平滑肌松弛,用于治疗男性勃起功能障碍。虽然它们对 PDE5 具有高度特异性,但这些抑制剂也被怀疑与环腺苷酸 (cAMP) 特异性 PDE 交叉相互作用,导致这种环核苷酸的细胞内积累和相关睾酮增加,对男性生殖参数产生积极影响。然而,PDE5i 的使用与 cAMP 介导的类固醇生成的激活之间的联系仍不清楚。我们研究了三种 PDE5i(西地那非、他达拉非和伐地那非)是否与高亲和力 cAMP 特异性酶 8A 和 8B 磷酸二酯酶 (PDE8A 和 PDE8B) 交叉相互作用,在体外转染的小鼠莱迪希细胞瘤 (mLTC1) 和人胚肾 (HEK293) 细胞系中。还评估了 PDE5i 诱导的 cAMP 依赖性睾酮及其前体孕酮的产生。我们开发了 PDE8A/B 生物传感器并修饰了环核苷酸,在我们的细胞模型中证实了酶与 cAMP 而不是 cGMP 的结合。细胞用 PDE5i 处理后,cAMP 与 PDE8A/B 的结合被置换,表明西地那非、他达拉非和伐地那非在活细胞中的作用效果相似。PDE5i 与 PDE8A/B 的交叉相互作用支持与 cGMP 增加一起发生的促性腺激素增强的细胞内 cAMP 增加,以及类固醇合成。事实上,我们发现 PDE5i 处理莱迪希细胞会增加促性腺激素触发的孕酮和睾酮的产生。我们证明 PDE5i 可能与 cAMP 特异性 PDE8A 和 PDE8B 相互作用,可能导致细胞内 cAMP 和性激素增加。这些发现支持临床数据表明 PDE5i 可能增加男性的睾酮水平。