Sandrini Maurizio, Vitale Giovanni, Pini Luigi Alberto, Lopetuso Giuseppe, Romualdi Patrizia, Candeletti Sanzio
Department of Biomedical Sciences, Section of Pharmacology, Italy.
Eur J Pharmacol. 2005 Jan 10;507(1-3):43-8. doi: 10.1016/j.ejphar.2004.11.030. Epub 2004 Dec 15.
Nociceptin/orphanin FQ (N/OFQ) is involved in many behavioural patterns; in particular, it exerts a modulating effect on nociception. Like other proposed antiopiates, nociceptin/orphanin FQ has been shown to have analgesic, hyperalgesic as well as antianalgesic properties. Among the various effects proposed on nociceptive sensitivity at supraspinal level, the antagonistic activity toward morphine analgesia seems to be of interest. Therefore, we decided to investigate whether nociceptin/orphanin FQ and [Arg14, Lys15] nociceptin/orphanin FQ (R-K, a nociceptin analogue) can have the same effect on the analgesia produced by nonopioid analgesics. In this study, we examined the antianalgesic effect of nociceptin/orphanin FQ and its analogue R-K on paracetamol-induced analgesia and evaluated by means of the hot plate test in rats. Nociceptin/orphanin FQ was intracerebroventricularly administered, and, after 5 min, a dose of 400 mg/kg paracetamol was injected intraperitoneally, 30 min before the hot plate test. Nociceptin/orphanin FQ and R-K showed a dose-dependent antagonism on the antinociceptive effect of paracetamol, and the activity of both drugs was significantly reduced by the antagonist [Nphe1] Arg14, Lys15-N/OFQ-NH2 (UFP-101). These data indicate that nociceptin/orphanin FQ and R-K have an antianalgesic effect on the analgesia produced by a nonopioid analgesic drug, like paracetamol, that seems to develop within the brain.
痛敏肽/孤啡肽FQ(N/OFQ)参与多种行为模式;特别是,它对痛觉产生调节作用。与其他提出的抗阿片类药物一样,痛敏肽/孤啡肽FQ已被证明具有镇痛、痛觉过敏以及抗镇痛特性。在对脊髓上水平痛觉敏感性提出的各种作用中,对吗啡镇痛的拮抗活性似乎值得关注。因此,我们决定研究痛敏肽/孤啡肽FQ和[精氨酸14,赖氨酸15]痛敏肽/孤啡肽FQ(R-K,一种痛敏肽类似物)对非阿片类镇痛药产生的镇痛作用是否具有相同效果。在本研究中,我们通过大鼠热板试验,研究了痛敏肽/孤啡肽FQ及其类似物R-K对扑热息痛诱导的镇痛作用的抗镇痛效果。将痛敏肽/孤啡肽FQ经脑室注射给药,5分钟后,在热板试验前30分钟腹腔注射400mg/kg扑热息痛。痛敏肽/孤啡肽FQ和R-K对扑热息痛的镇痛作用表现出剂量依赖性拮抗作用,并且两种药物的活性均被拮抗剂[苯丙氨酸1]精氨酸14,赖氨酸15-N/OFQ-NH2(UFP-101)显著降低。这些数据表明,痛敏肽/孤啡肽FQ和R-K对非阿片类镇痛药如扑热息痛产生的镇痛作用具有抗镇痛作用,这种作用似乎在脑内产生。