Development of κ Opioid Receptor Antagonists

被引:131
|
作者
Carroll, F. Ivy [1 ]
Carlezon, William A., Jr. [2 ]
机构
[1] Res Triangle Inst, Ctr Organ & Med Chem, Res Triangle Pk, NC 27709 USA
[2] Harvard Univ, Sch Med, McLean Hosp, Dept Psychiat, Belmont, MA 02478 USA
关键词
CORTICOTROPIN-RELEASING-FACTOR; SELF-ADMINISTRATION BEHAVIOR; DRUG-INDUCED REINSTATEMENT; ELEMENT-BINDING PROTEIN; BINALTORPHIMINE NOR-BNI; ANXIETY-LIKE BEHAVIOR; FORCED SWIM TEST; NUCLEUS-ACCUMBENS; COCAINE-SEEKING; PHARMACOLOGICAL CHARACTERIZATION;
D O I
10.1021/jm301783x
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
kappa opioid receptors (KORs) belong to the G-protein-coupled class of receptors (GPCRs). They are activated by the endogenous opioid peptide dynorphin (DYN) and expressed at particularly high levels within brain areas implicated in modulation of motivation, emotion, and cognitive function. Chronic activation of KORs in animal models has maladaptive effects including increases in behaviors that reflect depression, the propensity to engage in drug-seeking behavior, and drug craving. The fact that KOR activation has such a profound influence on behaviors often triggered by stress has led to interest in selective KOR antagonists as potential therapeutic agents. This Perspective provides a description of preclinical research conducted in the development of several different classes of selective KOR antagonists, a summary of the clinical studies conducted thus far, and recommendations for the type of work needed in the future to determine if these agents would be useful as pharmacotherapies for neuropsychiatric illness.
引用
收藏
页码:2178 / 2195
页数:18
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