Department of Pathology, LSU Health Sciences Center-Shreveport, LA, USA.
Cardiovasc Res. 2012 Jul 1;95(1):7-18. doi: 10.1093/cvr/cvs143. Epub 2012 Apr 5.
Although an abundant amount of research has been devoted to the study of angiogenesis, its precise mechanisms are incompletely understood. Numerous clinical trials focused on therapeutic angiogenesis for the treatment of tissue ischaemia have not been as successful as those of preclinical studies. Thus, additional studies are needed to better understand critical molecular mechanisms regulating ischaemic neovascularization to identify novel therapeutic agents. Nitric oxide (NO) plays a central role in ischaemic neovascularization through the generation of cyclic guanosine monophosphate (cGMP) and the activation of several other signalling responses. Accumulated evidence suggests that endothelial protein kinase A/endothelial NO synthase (PKA/eNOS) signalling may play an important role in ischaemic disorders by promoting neovascularization. This review highlights recent advances in the role of the PKA/eNOS and NO-cGMP-kinase cascade pathway in ischaemic neovascularization. We also discuss molecular relationships of PKA/eNOS with other angiogenic pathways and explore the possibility of activation of the NO/nitrite endocrine system as potential therapeutic targets for ischaemic angiogenesis.
尽管已经有大量研究致力于研究血管生成,但它的确切机制仍不完全清楚。许多专注于治疗性血管生成以治疗组织缺血的临床试验并没有像临床前研究那样成功。因此,需要进一步的研究来更好地了解调节缺血性血管新生的关键分子机制,以确定新的治疗剂。一氧化氮 (NO) 通过生成环鸟苷酸 (cGMP) 和激活其他几种信号反应,在缺血性血管新生中发挥核心作用。越来越多的证据表明,内皮蛋白激酶 A/内皮一氧化氮合酶 (PKA/eNOS) 信号可能通过促进血管新生在缺血性疾病中发挥重要作用。这篇综述强调了 PKA/eNOS 和 NO-cGMP-激酶级联途径在缺血性血管新生中的作用的最新进展。我们还讨论了 PKA/eNOS 与其他血管生成途径的分子关系,并探讨了激活 NO/亚硝酸盐内分泌系统作为缺血性血管生成潜在治疗靶点的可能性。