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Differential Modulation of Ventral Tegmental Area Circuits by the Nociceptin/Orphanin FQ System.孤啡肽/强啡肽系统对腹侧被盖区回路的差异调节。
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本文引用的文献

1
MT-7716, a novel selective nonpeptidergic NOP receptor agonist, effectively blocks ethanol-induced increase in GABAergic transmission in the rat central amygdala.MT-7716,一种新型选择性非肽类 NOP 受体激动剂,能有效阻断乙醇诱导的大鼠中枢杏仁核 GABA 能传递的增加。
Front Integr Neurosci. 2014 Feb 18;8:18. doi: 10.3389/fnint.2014.00018. eCollection 2014.
2
Cluster and meta-analyses on factors influencing stress-induced alcohol drinking and relapse in rodents.关于影响啮齿动物应激诱导饮酒和复发因素的聚类分析和荟萃分析。
Addict Biol. 2014 Mar;19(2):225-32. doi: 10.1111/adb.12125.
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Profiling of childhood adversity-associated DNA methylation changes in alcoholic patients and healthy controls.分析酒精患者和健康对照者中与童年逆境相关的 DNA 甲基化变化。
PLoS One. 2013 Jun 14;8(6):e65648. doi: 10.1371/journal.pone.0065648. Print 2013.
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Translational approach to develop novel medications on alcohol addiction: focus on neuropeptides.从翻译角度探索新型酒精成瘾药物研发:聚焦神经肽。
Curr Opin Neurobiol. 2013 Aug;23(4):684-91. doi: 10.1016/j.conb.2013.04.009. Epub 2013 May 3.
5
The role of NOP receptors in psychomotor stimulation and locomotor sensitization induced by cocaine and amphetamine in mice.NOP 受体在可卡因和安非他命诱导的小鼠精神运动刺激和运动敏化中的作用。
Eur J Pharmacol. 2013 May 5;707(1-3):41-5. doi: 10.1016/j.ejphar.2013.03.021. Epub 2013 Mar 21.
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Stress-related neuropeptides and addictive behaviors: beyond the usual suspects.应激相关神经肽与成瘾行为:超越常见的嫌疑对象。
Neuron. 2012 Oct 4;76(1):192-208. doi: 10.1016/j.neuron.2012.09.026.
7
Modification of anxiety-like behaviors by nociceptin/orphanin FQ (N/OFQ) and time-dependent changes in N/OFQ-NOP gene expression following ethanol withdrawal.内阿片肽/孤啡肽(N/OFQ)对焦虑样行为的修饰作用及乙醇戒断后 N/OFQ-NOP 基因表达的时程变化。
Addict Biol. 2013 May;18(3):467-79. doi: 10.1111/j.1369-1600.2012.00466.x. Epub 2012 Jul 15.
8
Brain and whole-body imaging of nociceptin/orphanin FQ peptide receptor in humans using the PET ligand 11C-NOP-1A.利用 PET 配体 11C-NOP-1A 对人类的孤啡肽受体进行脑和全身成像。
J Nucl Med. 2012 Mar;53(3):385-92. doi: 10.2967/jnumed.111.097162. Epub 2012 Feb 6.
9
Nociceptin/orphanin FQ blockade of corticotropin-releasing factor-induced gamma-aminobutyric acid release in central amygdala is enhanced after chronic ethanol exposure.慢性乙醇暴露后,孤啡肽/强啡肽 FQ 对中央杏仁核中促肾上腺皮质激素释放因子诱导的γ-氨基丁酸释放的阻断作用增强。
Biol Psychiatry. 2012 Apr 15;71(8):666-76. doi: 10.1016/j.biopsych.2011.10.032. Epub 2011 Dec 6.
10
Brain and whole-body imaging in rhesus monkeys of 11C-NOP-1A, a promising PET radioligand for nociceptin/orphanin FQ peptide receptors.恒河猴脑及全身成像研究 11C-NOP-1A,一种有前景的孤啡肽/强啡肽 A 肽受体正电子发射断层扫描配体。
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新型脑渗透性选择性NOP受体激动剂MT-7716的长期治疗可减少大鼠的酒精摄入和觅酒行为。

Chronic treatment with novel brain-penetrating selective NOP receptor agonist MT-7716 reduces alcohol drinking and seeking in the rat.

作者信息

Ciccocioppo Roberto, Stopponi Serena, Economidou Daina, Kuriyama Makoto, Kinoshita Hiroshi, Heilig Markus, Roberto Marisa, Weiss Friedbert, Teshima Koji

机构信息

Pharmacology Unit, School of Pharmacy, University of Camerino, Camerino, Italy.

Department II (CNS), Pharmacology Research Laboratories I, Research Division, Mitsubishi Tanabe Pharma Corporation, Yokohama, Japan.

出版信息

Neuropsychopharmacology. 2014 Oct;39(11):2601-10. doi: 10.1038/npp.2014.113. Epub 2014 Jun 27.

DOI:10.1038/npp.2014.113
PMID:24863033
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4207340/
Abstract

Since its discovery, the nociceptin/orphanin FQ (N/OFQ)-NOP receptor system has been extensively investigated as a promising target to treat alcoholism. Encouraging results obtained with the endogenous ligand N/OFQ stimulated research towards the development of novel brain-penetrating NOP receptor agonists with a pharmacological and toxicological profile compatible with clinical development. Here we describe the biochemical and alcohol-related behavioral effects of the novel NOP receptor agonist MT-7716. MT-7716 has high affinity for human NOP receptors expressed in HEK293 cells with a Ki value of 0.21 nM. MT-7716 concentration-dependently stimulated GTPγ(35)S binding with an EC50 value of 0.30 nM and its efficacy was similar to N/OFQ, suggesting that MT7716 is a full agonist at NOP receptors. In the two bottle choice test MT-7716 (0, 0.3, 1, and 3 mg/kg, bid) given orally for 14 days dose-dependently decreased voluntary alcohol intake in Marchigian Sardinian rats. The effect became gradually stronger following repeated administration, and was still significant 1 week after discontinuation of the drug. Oral naltrexone (30 mg/kg, bid) for 14 days also reduced ethanol intake; however, the effect decreased over the treatment period and rapidly disappeared when drug treatment was discontinued. MT-7716 is also effective for preventing reinstatement caused by both ethanol-associated environmental stimuli and stress. Finally, to investigate the effect of MT-7716 on alcohol withdrawal symptoms, Wistar rats were withdrawn from a 7-day alcohol liquid diet. MT-7716 significantly attenuated somatic alcohol withdrawal symptoms. Together these findings indicate that MT-7716 is a promising candidate for alcoholism treatment remaining effective with chronic administration.

摘要

自被发现以来,痛敏肽/孤啡肽FQ(N/OFQ)-NOP受体系统作为治疗酒精中毒的一个有前景的靶点,已得到广泛研究。内源性配体N/OFQ所取得的令人鼓舞的结果激发了对开发具有与临床开发相兼容的药理学和毒理学特征的新型脑渗透性NOP受体激动剂的研究。在此,我们描述新型NOP受体激动剂MT-7716的生化及与酒精相关的行为学效应。MT-7716对在HEK293细胞中表达的人NOP受体具有高亲和力,其Ki值为0.21 nM。MT-7716浓度依赖性地刺激GTPγ(35)S结合,EC50值为0.30 nM,其效能与N/OFQ相似,表明MT7716是NOP受体的完全激动剂。在双瓶选择试验中,给Marchigian撒丁岛大鼠口服MT-7716(0、0.3、1和3 mg/kg,每日两次),持续14天,剂量依赖性地降低了其自愿酒精摄入量。重复给药后,这种效应逐渐增强,停药1周后仍很显著。口服纳曲酮(30 mg/kg,每日两次),持续14天,也减少了乙醇摄入量;然而,这种效应在治疗期间逐渐减弱,停药后迅速消失。MT-7716对预防由乙醇相关环境刺激和应激引起的复吸也有效。最后,为了研究MT-7716对酒精戒断症状的影响,将Wistar大鼠从7天的酒精液体饮食中撤药。MT-7716显著减轻了躯体酒精戒断症状。这些研究结果共同表明,MT-7716是治疗酒精中毒的一个有前景的候选药物,长期给药仍有效。