ENHANCED ANTIOPIATE ACTIVITY IN PEPTIDOMIMETICS OF FMRFAMIDE CONTAINING Z-2,3-METHANOMETHIONINE

被引:38
作者
MALIN, DH
PAYZA, K
LAKE, JR
CORRIERE, LS
BENSON, TM
SMITH, DA
KELLEY, RS
HO, KK
BURGESS, K
机构
[1] NIMH, WASHINGTON, DC 20032 USA
[2] RICE UNIV, HOUSTON, TX 77251 USA
关键词
FMRFA; NPFF; NPFF RECEPTORS; NEUROPEPTIDE FF; F8FAMIDE; ANTIOPIATE PEPTIDES; CYCLOPROPYLOGS; PEPTIDOMIMETICS; RAT; OPIATE DEPENDENCE; OPIATE ABSTINENCE SYNDROME;
D O I
10.1016/0196-9781(93)90009-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
FMRFa is a molluscan peptide that has shown antiopiate activity in a number of mammalian test systems. The current study determined the antiopiate potency of FMRFa and two conformationally constrained peptidomimetics of FMRFa containing stereoisomers of Z-2,3-methanomethionine. Morphine abstinence sips were observed after varying doses (0.25-25.0 mug) of these substances were injected into the third ventricle of morphine-dependent rats. Although both peptidomimetics were far more potent than FMRFa itself, they bound with lower affinity than FMRFa to rat spinal cord receptors for the mammalian FMRFa-like peptide, NPFF.
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页码:47 / 51
页数:5
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