Horm Metab Res. 2012 Sep;44(10):713-5. doi: 10.1055/s-0031-1301327. Epub 2012 Sep 5.
Cyclic nucleotides cAMP and cGMP are part of almost all major cellular signaling pathways. Phosphodiesterases (PDEs) are enzymes that regulate the intracellular levels of cAMP and cGMP. Protein kinase A or cAMP-dependent protein kinase mediates most cAMP effects in the cell. Over the last 25 years, various components of this group of molecules have been involved in human diseases, both genetic and acquired. Lately, the PDEs attract more attention. The pharmacological exploitation of the PDE's ability to regulate cGMP and cAMP, and through them, a variety of signaling pathways, has led to a number of new drugs for diverse applications from the treatment of erectile dysfunction to heart failure, asthma, and chronic obstructive pulmonary disease. We present the abstracts (available online) and selected articles from the proceedings of a meeting that took place at the National Institutes of Health (NIH), Bethesda, MD, June 8-10, 2011.
环核苷酸 cAMP 和 cGMP 几乎是所有主要细胞信号通路的组成部分。磷酸二酯酶 (PDEs) 是调节细胞内 cAMP 和 cGMP 水平的酶。蛋白激酶 A 或 cAMP 依赖性蛋白激酶介导细胞中大多数 cAMP 效应。在过去的 25 年中,该分子群的各种成分都与遗传和获得性人类疾病有关。最近,PDEs 引起了更多的关注。通过药理学利用 PDE 调节 cGMP 和 cAMP 的能力,以及通过它们调节各种信号通路,已经开发出许多用于从治疗勃起功能障碍到心力衰竭、哮喘和慢性阻塞性肺疾病等多种用途的新药。我们展示了 2011 年 6 月 8 日至 10 日在马里兰州贝塞斯达的美国国立卫生研究院 (NIH) 举行的会议的摘要(可在线获取)和精选文章。