Autonomic Neuroscience Centre, Royal Free and University College Medical School, Rowland Hill Street, London, UK.
Br J Pharmacol. 2012 Sep;167(2):238-55. doi: 10.1111/j.1476-5381.2012.02008.x.
There has been a remarkable growth of papers published about purinergic signalling via ATP since 1972. I am most grateful to the wonderful PhD students and postdoctoral fellows who have worked with me over the years to pursue the purinergic hypothesis despite early opposition and to the many outstanding scientists around the world who are currently extending the story. Recently, therapeutic approaches to pathological disorders include the development of selective P1 and P2 receptor subtype agonists and antagonists, as well as of inhibitors of extracellular ATP breakdown and of ATP transport enhancers and inhibitors. Medicinal chemists are starting to develop small molecule purinergic drugs that are orally bioavailable and stable in vivo.
自 1972 年以来,有关通过 ATP 进行嘌呤能信号传递的论文数量显著增长。我非常感谢多年来与我一起研究嘌呤能假说的出色的博士生和博士后研究员,尽管他们早期曾遭遇反对,也要感谢世界各地目前正在拓展这一领域的众多杰出科学家。最近,针对病理疾病的治疗方法包括开发选择性 P1 和 P2 受体亚型激动剂和拮抗剂,以及抑制细胞外 ATP 分解、ATP 转运增强剂和抑制剂。药物化学家开始开发口服生物利用度高且体内稳定的小分子嘌呤能药物。