首页> 外文期刊>European Journal of Pharmacology: An International Journal >Nociceptin/orphanin FQ blocks the antinociception induced by mu, kappa and delta opioid agonists on the cold water tail-flick test.
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Nociceptin/orphanin FQ blocks the antinociception induced by mu, kappa and delta opioid agonists on the cold water tail-flick test.

机译:Nociceptin / orphanin FQ在冷水甩尾试验中阻断了mu,kappa和delta类阿片激动剂诱导的抗伤害感受。

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摘要

Nociceptin/orphanin FQ (N/OFQ), a 17-amino-acid peptide, is an endogenous agonist whose receptor is similar in sequence to mu, delta and kappa opioid receptors. It has been reported that N/OFQ can block antinociceptive effects induced by opioid receptor agonists in the radiant heat tail-flick test and warm water tail-withdrawal test. The present study was designed to see the effect of N/OFQ on antinociception induced by opioid receptor agonists in the cold water tail-flick (CWT) test, which measures a different type of pain. In adult male Sprague-Dawley (S-D) rats given subcutaneous (s.c.) injections of saline or morphine (8 mg/kg), intracerebroventricular (i.c.v.) injection of N/OFQ (18 microg) 15 min later produced a significant reversal of morphine antinociception (P<0.01, ANOVA followed by Duncan's test), compared to the corresponding saline control group. Saline (t=+15 min, i.c.v.) had no effect on s.c. morphine antinociception (P>0.01), compared to the corresponding saline control group. When thekappa opioid receptor agonist spiradoline (80 mg/kg, s.c.) was used instead of morphine, similar results were observed. In another series of experiments, it was found that i.c.v. injection of N/OFQ (18 microg) reversed the antinociception induced by i.c.v. injection of the selective mu opioid agonist PL017 (2 microg), delta opioid agonist DPDPE (50 ng) and kappa opioid agonist dynorphin (21.5 microg), respectively. These results indicate that N/OFQ may be an endogenous anti-opioid peptide in the brain of rats in the CWT test.
机译:Nociceptin / orphanin FQ(N / OFQ)是一种17个氨基酸的肽,是一种内源性激动剂,其受体与mu,delta和kappa类阿片受体的序列相似。据报道,在辐射热甩尾试验和温水抽尾试验中,N / OFQ可以阻止阿片受体激动剂引起的抗伤害作用。本研究的目的是在冷水甩尾(CWT)试验中观察N / OFQ对阿片受体激动剂诱导的抗伤害感受的作用,该试验可测量不同类型的疼痛。在成年雄性Sprague-Dawley(SD)大鼠中,皮下(sc)注射生理盐水或吗啡(8 mg / kg),脑室内(icv)注射N / OFQ(18 microg)15分钟后产生明显的吗啡抗伤害感受力逆转。 (P <0.01,ANOVA,然后进行邓肯检验),与相应的生理盐水对照组相比。盐水(t = + 15分钟,i.c.v。)对s.c没有影响。与相应的生理盐水对照组相比,吗啡具有抗伤害作用(P> 0.01)。当使用κ阿片受体激动剂螺环索林(80 mg / kg,s.c.)代替吗啡时,观察到相似的结果。在另一组实验中,发现i.c.v.注射N / OFQ(18微克)可逆转i.c.v.分别注射选择性μ阿片类激动剂PL017(2微克),δ阿片类激动剂DPDPE(50 ng)和κ阿片类激动剂强啡肽(21.5微克)。这些结果表明,在CWT测试中,N / OFQ可能是大鼠大脑中的内源性抗阿片肽。

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