首页> 外文期刊>Peptides: An International Journal >Lack of tolerance and morphine-induced cross-tolerance to the analgesia of chimeric peptide of Met-enkephalin and FMRFa.
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Lack of tolerance and morphine-induced cross-tolerance to the analgesia of chimeric peptide of Met-enkephalin and FMRFa.

机译:Met-脑啡肽和FMRFa嵌合肽的镇痛作用缺乏耐受性和吗啡诱导的交叉耐受性。

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摘要

Chimeric peptide of Met-enkephalin and FMRFa (YGGFMKKKFMRFa-YFa), a kappa-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 kappa receptor agonist peptide dynorphin A(1-13) [DynA(1-13)]. Cross-tolerance effects between YFa and DynA(1-13) analgesia were also not observed on day 5. 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(1-13) 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.
机译:Met-脑啡肽和FMRFa的嵌合肽(YGGFMKKKFMRFa-YFa)是一种阿片类鸦片受体特异性肽,在用YFa或吗啡预处理4天后第5天没有诱导对其镇痛作用的耐受性和交叉耐受性。然而,用YFa预处理4天导致对吗啡镇痛作用的交叉耐受性的发展,并且吗啡预处理4天也导致对其自身镇痛作用的耐受性表达。当将YFa与Kappa受体激动剂肽强啡肽A(1-13)[DynA(1-13)]比较时,也观察到了相似的耐受性和交叉耐受性表达。在第5天也没有观察到YFa和DynA(1-13)镇痛之间的交叉耐受作用。有趣的是,当对YFa和DynA(1-13)进行5天的镇痛效果测试时,第3天的镇痛减少了。在DynA(1-13)的情况下观察到,而YFa止痛持续5天。因此,嵌合肽YFa可以用作了解疼痛调节以及与其他阿片类药物的耐受性和交叉耐受行为表达的有用探针。

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