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
相关论文
共 135 条
  • [1] Identification of stabilized dynorphin derivatives for suppressing tolerance in morphine-dependent rats
    Al-Fayoumi, SI
    Brugos, B
    Arya, V
    Mulder, E
    Eppler, B
    Mauderli, AP
    Hochhaus, G
    [J]. PHARMACEUTICAL RESEARCH, 2004, 21 (08) : 1450 - 1456
  • [2] Aldrich J., 2003, Burger's Medicinal Chemistry and Drug Discovery, V6th, P329, DOI DOI 10.1002/0471266949.BMC100
  • [3] Aldrich Jane V., 2009, P103, DOI 10.1201/9781420061161-c5
  • [4] ALDRICH JV, 2008, P 4 INT PEPT S
  • [5] Barber A, 1997, Expert Opin Investig Drugs, V6, P1351, DOI 10.1517/13543784.6.10.1351
  • [6] EVALUATION OF DELAYED TREATMENT OF FOCAL CEREBRAL-ISCHEMIA WITH 3 SELECTIVE KAPPA-OPIOID AGONISTS IN CATS
    BASKIN, DS
    WIDMAYER, MA
    BROWNING, JL
    HEIZER, ML
    SCHMIDT, WK
    [J]. STROKE, 1994, 25 (10) : 2047 - 2053
  • [7] Differential effects of the novel kappa opioid receptor antagonist, JDTic, on reinstatement of cocaine-seeking induced by footshock stressors vs cocaine primes and its antidepressant-like effects in rats
    Beardsley, PM
    Howard, JL
    Shelton, KL
    Carroll, FI
    [J]. PSYCHOPHARMACOLOGY, 2005, 183 (01) : 118 - 126
  • [8] Identification of arodyn, a novel acetylated dynorphin A-(1-11) analogue, as a κ opioid receptor antagonist
    Bennett, MA
    Murray, TF
    Aldrich, JV
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2002, 45 (26) : 5617 - 5619
  • [9] Anti-inflammatory effects of contralateral administration of the κ-opioid agonist U-50,488H in rats with unilaterally induced adjuvant arthritis
    Bileviciute-Ljungar, I
    Saxne, T
    Spetea, M
    [J]. RHEUMATOLOGY, 2006, 45 (03) : 295 - 302
  • [10] Analgesic and antiinflammatory effects of two novel κ-opioid peptides
    Binder, W
    Machelska, H
    Mousa, S
    Schmitt, T
    Rivière, PJM
    Junien, JL
    Stein, C
    Schäfer, M
    [J]. ANESTHESIOLOGY, 2001, 94 (06) : 1034 - 1044