首页> 外文期刊>Neuropharmacology >The ORL-1 (NOP(1)) receptor ligand nociceptin/orphanin FQ (N/OFQ) inhibits neurogenic dural vasodilatation in the rat.
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The ORL-1 (NOP(1)) receptor ligand nociceptin/orphanin FQ (N/OFQ) inhibits neurogenic dural vasodilatation in the rat.

机译:ORL-1(NOP(1))受体配体伤害感受素/孤啡肽FQ(N / OFQ)抑制大鼠的神经源性硬脑膜血管舒张。

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摘要

The effects of the ORL-1 (NOP(1)) receptor ligand nociceptin (N/OFQ) and the nociceptin antagonists [Nphe(1)]N/OFQ-(1-13)-NH(2) (Nphe) and nocistatin (NST) on neurogenic dural vasodilatation (NDV) in the rat dura mater evoked by electrical stimulation of a closed cranial window were studied. The middle meningeal artery was visualised using intravital microscopy, and the vessel diameter analysed using a video dimension analyser. N/OFQ (1, 10, 100 nmol kg(-1); i.v., n=10) significantly and dose-dependently suppressed NDV maximally by 65% (P<0.01). Neither Nphe (100 nmol kg(-1); n=5) nor NST (100 nmol kg(-1); n=4) alone had an effect on NDV (P>0.05). Baseline vessel diameter was not significantly affected by application of N/OFQ, NST or Nphe. Application of the selective N/OFQ antagonist Nphe (10, 100 nmol kg(-1) i.v., n=8) dose-dependently and significantly (P<0.01) reversed the inhibition of NDV induced by application of N/OFQ (10 nmol kg(-1)). NST (10, 100 nmol kg(-1); n=7) failed to reverse the effects elicited by N/OFQ. Application of N/OFQ elicited a dose-dependent transient decrease in arterial blood pressure (P<0.01). Nphe dose-dependently reversed the cardiovascular effects induced by application of N/OFQ (10 nmol kg(-1)) (P<0.01),while NST did not alter the blood pressure reaction elicited by N/OFQ. The results show that N/OFQ inhibits NDV, an effect which is antagonised by Nphe, but not by NST. ORL-1 (NOP(1)) receptors located on trigeminal sensory fibres may be involved in the regulation of dural vessel diameter and hence may play a role in migraine pathophysiology.
机译:ORL-1(NOP(1))受体配体伤害感受器(N / OFQ)和伤害感受器拮抗剂[Nphe(1)] N / OFQ-(1-13)-NH(2)(Nphe)和伤害抑制素的作用(NST)对通过闭合颅窗电刺激诱发的大鼠硬脑膜神经源性硬脑膜血管舒张(NDV)的研究。使用活体显微镜观察脑膜中动脉,并使用视频尺寸分析仪分析血管直径。 N / OFQ(1,10,100 nmol kg(-1); i.v.,n = 10)显着且剂量依赖性地将NDV抑制最大65%(P <0.01)。 Nphe(100 nmol kg(-1); n = 5)和NST(100 nmol kg(-1); n = 4)都不会对NDV产生影响(P> 0.05)。使用N / OFQ,NST或Nphe对基线血管直径没有明显影响。选择性N / OFQ拮抗剂Nphe(10,100 nmol kg(-1)iv,n = 8)的剂量依赖性和显着性(P <0.01)的应用逆转了N / OFQ(10 nmol)诱导的对NDV的抑制作用千克(-1))。 NST(10,100 nmol kg(-1); n = 7)无法逆转N / OFQ引起的影响。 N / OFQ的应用引起动脉血压的剂量依赖性短暂降低(P <0.01)。 Nphe剂量依赖性地逆转了应用N / OFQ(10 nmol kg(-1))引起的心血管效应(P <0.01),而NST并没有改变N / OFQ引起的血压反应。结果表明,N / OFQ抑制了NDV,Nphe拮抗了NDV,但NST却没有。位于三叉神经感觉纤维上的ORL-1(NOP(1))受体可能参与硬脑膜血管直径的调节,因此可能在偏头痛的病理生理中起作用。

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