Peptide Kappa Opioid Receptor Ligands: Potential for Drug Development

被引:100
|
作者
Aldrich, Jane V. [1 ]
McLaughlin, Jay P. [2 ,3 ]
机构
[1] Univ Kansas, Dept Med Chem, Lawrence, KS 66045 USA
[2] Northeastern Univ, Dept Psychol, Boston, MA 02115 USA
[3] Torrey Pines Inst Mol Studies, Port St Lucie, FL 34987 USA
来源
AAPS JOURNAL | 2009年 / 11卷 / 02期
关键词
antidepressant; blood-brain barrier; cocaine abuse; dynorphin analogs; peptide metabolism; BLOOD-BRAIN-BARRIER; DYNORPHIN A(1-8) ANALOG; FORCED SWIM TEST; SALVINORIN-A; IN-VITRO; DISCRIMINATIVE STIMULUS; ANALGESIC PEPTIDE; DOPAMINE NEURONS; PLACE PREFERENCE; AGONIST;
D O I
10.1208/s12248-009-9105-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
While narcotic analgesics such as morphine, which act preferentially through mu opioid receptors, remain the gold standard in the treatment of severe pain, their use is limited by detrimental liabilities such as respiratory depression and drug dependence. Thus, there has been considerable interest in developing ligands for kappa opioid receptors (KOR) as potential analgesics and for the treatment of a variety of other disorders. These include effects mediated both by central receptors, such as antidepressant activity and a reduction in cocaine-seeking behavior, and activity resulting from the activation of peripheral receptors, such as analgesic and anti-inflammatory effects. While the vast majority of opioid receptor ligands that have progressed in preclinical development have been small molecules, significant advances have been made in recent years in identifying opioid peptide analogs that exhibit promising in vivo activity. This review will focus on possible therapeutic applications of ligands for KOR and specifically on the potential development of peptide ligands for these receptors.
引用
收藏
页码:312 / 322
页数:11
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