Adenosine receptors as drug targets - what are the challenges?

被引:721
作者
Chen, Jiang-Fan [1 ]
Eltzschig, Holger K. [2 ]
Fredholm, Bertil B. [3 ]
机构
[1] Boston Univ, Dept Neurol & Pharmacol, Sch Med, Boston, MA 02118 USA
[2] Univ Colorado, Dept Anesthesiol, Mucosal Inflammat Program, Sch Med, Aurora, CO 80045 USA
[3] Karolinska Inst, Dept Physiol & Pharmacol, S-17177 Stockholm, Sweden
基金
美国国家卫生研究院;
关键词
PROTEIN-COUPLED RECEPTOR; ACUTE HEART-FAILURE; ISCHEMIA-REPERFUSION INJURY; MARROW-DERIVED CELLS; BLOOD-BRAIN-BARRIER; INDUCIBLE FACTOR-I; FIND-ME SIGNAL; A(2A) RECEPTOR; PARKINSONS-DISEASE; A(1) RECEPTOR;
D O I
10.1038/nrd3955
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Adenosine signalling has long been a target for drug development, with adenosine itself or its derivatives being used clinically since the 1940s. In addition, methylxanthines such as caffeine have profound biological effects as antagonists at adenosine receptors. Moreover, drugs such as dipyridamole and methotrexate act by enhancing the activation of adenosine receptors. There is strong evidence that adenosine has a functional role in many diseases, and several pharmacological compounds specifically targeting individual adenosine receptors - either directly or indirectly - have now entered the clinic. However, only one adenosine receptor-specific agent - the adenosine A(2A) receptor agonist regadenoson (Lexiscan; Astellas Pharma) - has so far gained approval from the US Food and Drug Administration (FDA). Here, we focus on the biology of adenosine signalling to identify hurdles in the development of additional pharmacological compounds targeting adenosine receptors and discuss strategies to overcome these challenges.
引用
收藏
页码:265 / 286
页数:22
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