Lack of tolerance and morphine-induced cross-tolerance to the analgesia of chimeric peptide of Met-enkephalin and FMRFa

被引:10
作者
Gupta, Kshitij [1 ]
Vats, Ishwar Dutt [1 ]
Gupta, Yogendra Kumar [2 ]
Saleem, Kishwar [3 ]
Pasha, Santosh [1 ]
机构
[1] Inst Genom & Integrat Biol, Peptide Synth Lab, Delhi 110007, India
[2] All India Inst Med Sci, Dept Pharmacol, New Delhi 110029, India
[3] Jamia Millia Islamia, Fac Nat Sci, Dept Chem, New Delhi 110025, India
关键词
Tolerance; Cross-tolerance; Chimeric peptide (YFa); Dynorphin A(1-13); Analgesia;
D O I
10.1016/j.peptides.2008.09.013
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
Chimeric peptide of Met-enkephalin and FMRFa (YGGFMKKKFMRFa-YFa), a K-opioid receptor specific peptide, did not induce tolerance and cross-tolerance effects to its analgesic action on day 5 after pretreatment with either YFa or morphine for 4 days. However, pretreatment with YFa for 4 days led to the development of cross-tolerance to the analgesic effects of morphine and also 4 days of pretreatment of morphine resulted in the expression of tolerance to its own analgesic effects. Similar expression of tolerance and cross-tolerance were also observed when YFa was compared with the K receptor agonist peptide dynorphin A(1-13) [DynA(I-13)]. Cross-tolerance effects between YFa and DynA(1-13) analgesia were also not observed on day S. Interestingly, when YFa and DynA(1-13) were tested for their analgesic effects for 5 days, reduction in analgesia on day 3 was observed in case of DynA(113) whereas YFa maintained its analgesia for 5 days. Thus, chimeric peptide YFa may serve as a useful probe to understand pain modulation and expression of tolerance and cross-tolerance behavior with other opioids. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:2266 / 2275
页数:10
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