Mergia Evanthia, Koesling Doris, Friebe Andreas
Institut für Pharmakologie und Toxikologie, Medizinische Fakultät MA N1, Ruhr-Universität Bochum, Bochum, 44780, Germany.
Handb Exp Pharmacol. 2009(191):33-46. doi: 10.1007/978-3-540-68964-5_3.
The NO/cGMP signalling cascade has an important role in smooth muscle relaxation, inhibition of platelet aggregation and neuronal transmission. Although the function of the main NO receptor GC (NO-GC) is well established, the particular tasks of the NO receptor isoforms (NO-GC1 and NO-GC2) are unclear and NO targets other than NO-GC have been postulated. Mice deficient in either NO receptor isoform or with a complete lack of NO-GC are now available and allow new insights in NO/cGMP signalling. The first reports about the KO strains show that, outside the neuronal system, the NO-GC isoforms can substitute for each other, and that amazingly low cGMP increases are sufficient to induce smooth muscle relaxation. In the neuronal system, however, the NO-GC isoforms obviously serve distinct functions as both isoforms are required for long term potentiation. Analysis of the complete NO-GC KO provides evidence that the vasorelaxing and platelet-inhibiting effects of NO are solely mediated by NO-GC. Thus, NO-GC appears to be the only NO receptor in these two systems.
一氧化氮/环磷酸鸟苷(NO/cGMP)信号级联在平滑肌舒张、抑制血小板聚集和神经传递中发挥着重要作用。尽管主要的NO受体鸟苷酸环化酶(NO-GC)的功能已得到充分证实,但NO受体亚型(NO-GC1和NO-GC2)的具体作用仍不清楚,并且有人推测存在除NO-GC之外的NO靶点。目前已有缺乏任一NO受体亚型或完全缺乏NO-GC的小鼠,这为研究NO/cGMP信号传导提供了新的视角。关于基因敲除(KO)品系的首批报告表明,在神经系统之外,NO-GC亚型可以相互替代,而且令人惊讶的是,极低的cGMP增加量就足以诱导平滑肌舒张。然而,在神经系统中,NO-GC亚型显然发挥着不同的功能,因为长期增强作用需要这两种亚型。对完全缺失NO-GC的小鼠的分析表明,NO的血管舒张和抑制血小板作用仅由NO-GC介导。因此,在这两个系统中,NO-GC似乎是唯一的NO受体。