Discovery of purinergic signalling, the initial resistance and current explosion of interest

被引:65
作者
Burnstock, G. [1 ]
机构
[1] Royal Free & Univ Coll Med, Auton Neurosci Ctr, Sch Med, London NW3 2PF, England
关键词
ATP; adenosine; purinoceptors; pain; stroke; cancer; FAST SYNAPTIC-TRANSMISSION; CENTRAL-NERVOUS-SYSTEM; PIG URINARY-BLADDER; GUINEA-PIG; ATP RECEPTOR; TAENIA-COLI; EXTRACELLULAR ATP; SMOOTH MUSCLE; P2X RECEPTOR; ADENOSINE TRIPHOSPHATE;
D O I
10.1111/j.1476-5381.2012.02008.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:238 / 255
页数:18
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