Lindsley Craig W, Hopkins Corey R
Department of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center , Omaha, Nebraska 68198-6125, United States.
J Med Chem. 2017 Sep 14;60(17):7233-7243. doi: 10.1021/acs.jmedchem.7b00151. Epub 2017 May 17.
The dopamine D receptor garnered a great deal of interest in the early 1990s when studies showed the atypical antipsychotic clozapine possessed higher affinity for D, relative to other dopamine receptor subtypes, and that this activity might underlie the unique clinical efficacy of clozapine. Unfortunately, D antagonists that were developed for schizophrenia failed in the clinic. Thus, D fell out of favor as a therapeutic target, and work in this area was silent for decades. Recently, D ligands with improved selectivity for D against not only D but also other biogenic amine targets have emerged, and D is once again in the spotlight as a novel target for both addiction and Parkinson's disease (PD), as well as other emerging diseases. This report will review the historical data for D, review the known D ligands, and then highlight new data supporting a role for D inhibition in addiction, PD, and cancer.
20世纪90年代初,多巴胺D受体引起了广泛关注,当时的研究表明,非典型抗精神病药物氯氮平相对于其他多巴胺受体亚型,对D受体具有更高的亲和力,且这种活性可能是氯氮平独特临床疗效的基础。不幸的是,为治疗精神分裂症而开发的D受体拮抗剂在临床试验中失败了。因此,D受体作为治疗靶点不再受青睐,该领域的研究沉寂了数十年。最近,对D受体具有更高选择性的配体出现了,不仅对D受体有选择性,而且对其他生物胺靶点也有选择性,D受体作为成瘾、帕金森病(PD)以及其他新兴疾病的新靶点,再次成为焦点。本报告将回顾D受体的历史数据,介绍已知的D受体配体,然后重点阐述支持D受体抑制在成瘾、帕金森病和癌症中发挥作用的新数据。