Suppr超能文献

MP1104,一种混合的κ-δ阿片受体激动剂,具有抗可卡因特性,在大鼠中副作用减少。

MP1104, a mixed kappa-delta opioid receptor agonist has anti-cocaine properties with reduced side-effects in rats.

机构信息

School of Biological Sciences, Centre for Biodiscovery, Victoria University of Wellington, Wellington, New Zealand.

Molecular Pharmacology Program and Department of Neurology, Memorial Sloan Kettering Cancer Centre, New York, USA.

出版信息

Neuropharmacology. 2019 May 15;150:217-228. doi: 10.1016/j.neuropharm.2019.02.010. Epub 2019 Feb 13.

Abstract

Kappa opioid receptor (KOPr) agonists have preclinical anti-cocaine and antinociceptive effects. However, adverse effects including dysphoria, aversion, sedation, anxiety and depression limit their clinical development. MP1104, an analogue of 3-iodobenzoyl naltrexamine, is a potent dual agonist at KOPr and delta opioid receptor (DOPr), with full agonist efficacy at both these receptors. In this study, we evaluate the ability of MP1104 to modulate cocaine-induced behaviors and side-effects preclinically. In male Sprague-Dawley rats trained to self-administer cocaine, MP1104 (0.3 and 1 mg/kg) reduced cocaine-primed reinstatement of drug-seeking behavior and caused significant downward shift of the dose-response curve in cocaine self-administration tests (0.3 and 0.6 mg/kg). The anti-cocaine effects exerted by MP1104 are in part due to increased dopamine (DA) uptake by the dopamine transporter (DAT) in the dorsal striatum (dStr) and nucleus accumbens (NAc). MP1104 (0.3 and 0.6 mg/kg) showed no significant anxiogenic effects in the elevated plus maze, pro-depressive effects in the forced swim test, or conditioned place aversion. Furthermore, pre-treatment with a DOPr antagonist, led to MP1104 producing aversive effects. This data suggests that the DOPr agonist actions of MP1104 attenuate the KOPr-mediated aversive effects of MP1104. The overall results from this study show that MP1104, modulates DA uptake in the dStr and NAc, and exerts potent anti-cocaine properties in self-administration tests with reduced side-effects compared to pure KOPr agonists. This data supports the therapeutic development of dual KOPr/DOPr agonists to reduce the side-effects of selective KOPr agonists. This article is part of the Special Issue entitled 'Opioid Neuropharmacology: Advances in treating pain and opioid addiction'.

摘要

κ 阿片受体 (KOPr) 激动剂具有抗可卡因和镇痛的临床前作用。然而,包括烦躁、厌恶、镇静、焦虑和抑郁在内的不良反应限制了它们的临床发展。MP1104 是 3-碘苯甲酰基纳曲胺的类似物,是 KOPr 和 δ 阿片受体 (DOPr) 的双重激动剂,对这两种受体均具有完全激动剂的功效。在这项研究中,我们评估了 MP1104 调节可卡因诱导的行为和临床前副作用的能力。在经过训练以自我给予可卡因的雄性 Sprague-Dawley 大鼠中,MP1104(0.3 和 1mg/kg)减少了可卡因引发的觅药行为的复燃,并在可卡因自我给药测试中导致剂量-反应曲线显著向下移动(0.3 和 0.6mg/kg)。MP1104 发挥的抗可卡因作用部分归因于背侧纹状体 (dStr) 和伏隔核 (NAc) 中的多巴胺转运体 (DAT) 对多巴胺的摄取增加。MP1104(0.3 和 0.6mg/kg)在高架十字迷宫中没有表现出明显的焦虑作用,在强迫游泳试验中没有表现出促抑郁作用,也没有产生条件性位置厌恶。此外,预先给予 DOPr 拮抗剂会导致 MP1104 产生厌恶作用。这些数据表明,MP1104 的 DOPr 激动作用减弱了 MP1104 的 KOPr 介导的厌恶作用。这项研究的总体结果表明,MP1104 调节 dStr 和 NAc 中的多巴胺摄取,并在自我给药测试中发挥出强大的抗可卡因作用,与纯 KOPr 激动剂相比,副作用减少。这一数据支持开发双重 KOPr/DOPr 激动剂来减少选择性 KOPr 激动剂的副作用,以用于治疗。本文是题为“阿片神经药理学:治疗疼痛和阿片成瘾的进展”的特刊的一部分。

相似文献

引用本文的文献

10
Confronting the opioid crisis with basic research in neuropharmacology.用神经药理学基础研究应对阿片类药物危机。
Neuropharmacology. 2020 Apr;166:107972. doi: 10.1016/j.neuropharm.2020.107972. Epub 2020 Jan 17.

本文引用的文献

1
Multifunctional Opioid Ligands.多功能阿片样物质配体
Handb Exp Pharmacol. 2018;247:21-51. doi: 10.1007/164_2018_104.
2
Strategy for making safer opioids bolstered.更安全阿片类药物的制造策略得到加强。
Nature. 2018 Jan 18;553(7688):286-288. doi: 10.1038/d41586-018-00045-1.
9
New Technologies for Elucidating Opioid Receptor Function.用于阐明阿片受体功能的新技术。
Trends Pharmacol Sci. 2016 Apr;37(4):279-289. doi: 10.1016/j.tips.2016.01.001. Epub 2016 Jan 29.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验