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本文引用的文献

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Activation of Neuropeptide FF Receptors by Kisspeptin Receptor Ligands.亲吻素受体配体对神经肽FF受体的激活作用。
ACS Med Chem Lett. 2010 Oct 25;2(1):53-7. doi: 10.1021/ml1002053. eCollection 2011 Jan 13.
2
A novel 26RFa peptide containing both analgesic and anti-inflammatory functions from Chinese tree shrew.一种来自中国树鼩的具有镇痛和抗炎双重功能的新型26RFa肽。
Biochimie. 2014 Jul;102:112-6. doi: 10.1016/j.biochi.2014.02.014. Epub 2014 Mar 12.
3
Gonadotropin-inhibitory hormone promoter-driven enhanced green fluorescent protein expression decreases during aging in female rats.促性腺激素抑制激素启动子驱动的增强型绿色荧光蛋白表达在雌性大鼠衰老过程中减少。
Endocrinology. 2014 May;155(5):1944-55. doi: 10.1210/en.2013-1786. Epub 2014 Feb 28.
4
Endogenous mammalian RF-amide peptides, including PrRP, kisspeptin and 26RFa, modulate nociception and morphine analgesia via NPFF receptors.内源性哺乳动物RF-酰胺肽,包括促食欲素、亲吻素和26RFa,通过NPFF受体调节伤害感受和吗啡镇痛作用。
Neuropharmacology. 2013 Dec;75:164-71. doi: 10.1016/j.neuropharm.2013.07.012. Epub 2013 Aug 2.
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The anti-inflammatory potential of neuropeptide FF in vitro and in vivo.神经肽 FF 在体外和体内的抗炎潜力。
Peptides. 2013 Sep;47:124-32. doi: 10.1016/j.peptides.2013.07.003. Epub 2013 Jul 12.
6
Physiological Roles of GPR10 and PrRP Signaling.GPR10 和 PrRP 信号的生理作用。
Front Endocrinol (Lausanne). 2013 Mar 5;4:20. doi: 10.3389/fendo.2013.00020. eCollection 2013.
7
Kisspeptins and reproduction: physiological roles and regulatory mechanisms.亲吻素与生殖:生理作用和调节机制。
Physiol Rev. 2012 Jul;92(3):1235-316. doi: 10.1152/physrev.00037.2010.
8
GRK2 protein-mediated transphosphorylation contributes to loss of function of μ-opioid receptors induced by neuropeptide FF (NPFF2) receptors.GRK2 蛋白介导的转磷酸化有助于神经肽 FF(NPFF2)受体诱导的 μ 阿片受体功能丧失。
J Biol Chem. 2012 Apr 13;287(16):12736-49. doi: 10.1074/jbc.M111.314617. Epub 2012 Feb 28.
9
Hyperalgesic activity of kisspeptin in mice.在小鼠体内 kisspeptin 的痛觉过敏活性。
Mol Pain. 2011 Nov 23;7:90. doi: 10.1186/1744-8069-7-90.
10
Neuropeptide FF receptor modulates potassium currents in a dorsal root ganglion cell line.神经肽 FF 受体调节背根神经节细胞系中的钾电流。
Pharmacol Rep. 2011;63(4):1061-5. doi: 10.1016/s1734-1140(11)70623-5.

哺乳动物 RF-酰胺肽及其受体在调节啮齿动物痛觉中的作用。

Involvement of Mammalian RF-Amide Peptides and Their Receptors in the Modulation of Nociception in Rodents.

机构信息

UMR 7242 CNRS, Laboratory of Excellence Medalis, Biotechnologie et Signalisation Cellulaire, Université de Strasbourg , Illkirch , France.

出版信息

Front Endocrinol (Lausanne). 2014 Oct 2;5:158. doi: 10.3389/fendo.2014.00158. eCollection 2014.

DOI:10.3389/fendo.2014.00158
PMID:25324831
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4183120/
Abstract

Mammalian RF-amide peptides, which all share a conserved carboxyl-terminal Arg-Phe-NH2 sequence, constitute a family of five groups of neuropeptides that are encoded by five different genes. They act through five G-protein-coupled receptors and each group of peptide binds to and activates mostly one receptor: RF-amide related peptide group binds to NPFFR1, neuropeptide FF group to NPFFR2, pyroglutamylated RF-amide peptide group to QRFPR, prolactin-releasing peptide group to prolactin-releasing peptide receptor, and kisspeptin group to Kiss1R. These peptides and their receptors have been involved in the modulation of several functions including reproduction, feeding, and cardiovascular regulation. Data from the literature now provide emerging evidence that all RF-amide peptides and their receptors are also involved in the modulation of nociception. This review will present the current knowledge on the involvement in rodents of the different mammalian RF-amide peptides and their receptors in the modulation of nociception in basal and chronic pain conditions as well as their modulatory effects on the analgesic effects of opiates.

摘要

哺乳动物 RF-酰胺肽,它们都共享一个保守的羧基末端 Arg-Phe-NH2 序列,构成了由五个不同基因编码的五组神经肽家族。它们通过五个 G 蛋白偶联受体起作用,每组肽主要与一个受体结合并激活:RF-酰胺相关肽组与 NPFFR1 结合,神经肽 FF 组与 NPFFR2 结合,焦谷氨酸化 RF-酰胺肽组与 QRFPR 结合,催乳素释放肽组与催乳素释放肽受体结合,而 kisspeptin 组与 Kiss1R 结合。这些肽及其受体参与了多种功能的调节,包括生殖、进食和心血管调节。文献中的数据现在提供了新的证据,表明所有 RF-酰胺肽及其受体也参与了伤害感受的调节。这篇综述将介绍目前在啮齿动物中不同哺乳动物 RF-酰胺肽及其受体在基础和慢性疼痛条件下对伤害感受的调节,以及它们对阿片类药物镇痛作用的调节作用的知识。