En route to new blockbuster anti-histamines: surveying the offspring of the expanding histamine receptor family

被引:69
作者
Leurs, Rob [1 ]
Vischer, Henry F. [1 ]
Wijtmans, Maikel [1 ]
de Esch, Iwen J. P. [1 ]
机构
[1] Vrije Univ Amsterdam, Leiden Amsterdam Ctr Drug Res, Fac Sci, Amsterdam, Netherlands
关键词
H-3; RECEPTOR; CONSTITUTIVE ACTIVITY; THERAPEUTIC TARGET; MOLECULAR-CLONING; INVERSE AGONISM; SPLICE VARIANTS; BRAIN HISTAMINE; ANTAGONISTS; H-3-RECEPTOR; POTENT;
D O I
10.1016/j.tips.2011.02.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
With the recognition of two new histamine receptors at the start of the new millennium, the field of histamine research has seen a clear revival. In the last 10 years, many academic and industrial groups have taken up the challenge to target these new members of the aminergic G-protein-coupled receptor (GPCR) family. Histamine receptor research nicely illustrates how GPCR research has changed in the post-genomic era. There is a growing understanding of GPCR structure, function and modulation at a molecular level. Emerging concepts such as receptor isoforms, GPCR oligomerization and ligand-biased signaling are all being studied, but their clinical relevance remains to be determined. The histamine H-3 and H-4 drug development programs can help to establish the link between these molecular features and clinical efficacy. Several new anti-histamines are now being tested for diverse clinical applications and are poised to become the next blockbuster drugs targeting histamine receptors.
引用
收藏
页码:250 / 257
页数:8
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