Küthe Andrea, Reinecke Manfred, Uckert Stefan, Becker Armin, David Ivana, Heitland Aleksandra, Stief Christian G, Forssmann Wolf-Georg, Mägert Hans-Jürgen
Department of Urology, Hannover Medical School and IPF PharmaCeuticals, Hannover, Germany.
J Urol. 2003 May;169(5):1918-22. doi: 10.1097/01.ju.0000055602.35858.8f.
The induction of penile erection depends on the depletion of free intracellular Ca2+ from the cytosol into the sarcoplasmic reticulum of smooth muscle cells of the corpus cavernosum. This process is regulated by a complex system of signal transduction pathways. In this context guanylyl and adenylyl cyclases as well as cyclic nucleotide monophosphate degrading phosphodiesterases have essential roles and represent important target molecules for the development of drugs for erectile dysfunction. Sildenafil, which is an inhibitor of phosphodiesterase 5, is frequently used for this application but, unfortunately, it has undesirable side effects. Therefore, we investigated the suitability of membrane bound guanylyl cyclases as alternative target proteins.
We determined mRNA transcripts specific for guanylyl cyclase B, a receptor of the peptide hormone C-type natriuretic polypeptide, in human corpus cavernosum. We performed immunohistochemistry to evaluate the presence of guanylyl cyclase B in corpus cavernosum and helical artery smooth muscle cells. We further investigated whether C-type natriuretic polypeptide increases intracellular cyclic guanosine monophosphate and performed organ bath studies using corpus cavernosum muscle strips and C-type natriuretic polypeptide at concentrations of 1 to 1 microM.
mRNA transcripts were detected encoding for guanylyl cyclase-B, a receptor of the peptide hormone C-type natriuretic polypeptide, in human corpus cavernosum. This finding was verified at the protein level by immunohistochemistry that demonstrated guanylyl cyclase B in corpus cavernosum and helical artery smooth muscle cells. We further noted that C-type natriuretic polypeptide increased intracellular cyclic guanosine monophosphate. In organ bath studies with corpus cavernosum muscle strips C-type natriuretic polypeptide at concentrations of 1 to 1 microM. led to smooth muscle relaxation from 5% to 40%.
The results indicate a role for C-type natriuretic polypeptide and its receptor in the induction of penile erection and its possible future therapeutic use for erectile dysfunction.
阴茎勃起的诱导依赖于海绵体平滑肌细胞胞质溶胶中游离细胞内Ca2+向肌浆网的耗竭。这一过程由复杂的信号转导通路系统调节。在这种情况下,鸟苷酸环化酶和腺苷酸环化酶以及环核苷酸单磷酸降解磷酸二酯酶起着至关重要的作用,并且是勃起功能障碍药物开发的重要靶分子。西地那非是磷酸二酯酶5的抑制剂,常用于此用途,但不幸的是,它有不良副作用。因此,我们研究了膜结合鸟苷酸环化酶作为替代靶蛋白的适用性。
我们测定了人海绵体中鸟苷酸环化酶B(一种肽激素C型利钠肽的受体)的特异性mRNA转录本。我们进行了免疫组织化学,以评估海绵体和螺旋动脉平滑肌细胞中鸟苷酸环化酶B的存在。我们进一步研究了C型利钠肽是否会增加细胞内环磷酸鸟苷,并使用海绵体肌条和浓度为1至1微摩尔的C型利钠肽进行了器官浴研究。
在人海绵体中检测到编码鸟苷酸环化酶-B(一种肽激素C型利钠肽的受体)的mRNA转录本。免疫组织化学在蛋白质水平上证实了这一发现,该技术在海绵体和螺旋动脉平滑肌细胞中显示了鸟苷酸环化酶B。我们还注意到C型利钠肽增加了细胞内环磷酸鸟苷。在使用海绵体肌条的器官浴研究中,浓度为1至1微摩尔的C型利钠肽导致平滑肌松弛从5%至40%。
结果表明C型利钠肽及其受体在阴茎勃起诱导中起作用,并且其在未来可能用于治疗勃起功能障碍。