Abstract
Since the cloning of the histamine H3 receptor cDNA in 1999 by Lovenberg and co-workers, this histamine receptor has gained the interest of many pharmaceutical companies as a potential drug target for the treatment of various important disorders, including obesity, attention-deficit hyperactivity disorder, Alzheimer's disease, schizophrenia, as well as for myocardial ischaemia, migraine and inflammatory diseases. Here, we discuss relevant information on this target protein and describe the development of various H3 receptor agonists and antagonists, and their effects in preclinical animal models.
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CITATION STYLE
Leurs, R., Bakker, R. A., Timmerman, H., & de Esch, I. J. P. (2005, February). The histamine H3 receptor: From gene cloning to H3 receptor drugs. Nature Reviews Drug Discovery. https://doi.org/10.1038/nrd1631
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