MP-13, a novel chimeric peptide of morphiceptin and pepcan-9, produces potent antinociception with limited side effects

IF 2.5 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Chenxi Mei , Jing Zhang , Zhanyu Niu , Jerine Peter Simon , Tong Yang , Mingmin Huang , Zhonghua Zhang , Lanxia Zhou , Shouliang Dong
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Abstract

Pharmacological investigations have substantiated the potential of bifunctional opioid/cannabinoid agonists in delivering potent analgesia while minimizing adverse reactions. Peptide modulators of cannabinoid receptors, known as pepcans, have been investigated before. In this study, we designed a series of chimeric peptides based on pepcans and morphiceptin (YPFP-NH2). Here, we combined injections of pepcans and morphiceptin to investigate the combination treatment of opioids and cannabis and compared the analgesic effect with chimeric compounds. Subsequently, we employed computational docking to screen the compounds against opioid and cannabinoid receptors, along with an acute pain model, to identify the most promising peptide. Among these peptides, MP-13, a morphiceptin and pepcan-9 (PVNFKLLSH) construct, exhibited superior supraspinal analgesic efficacy in the tail-flick test, with an ED50 value at 1.43 nmol/mouse, outperforming its parent peptides and other chimeric analogs. Additionally, MP-13 displayed potent analgesic activity mediated by mu-opioid receptor (MOR), delta-opioid receptor (DOR), and cannabinoid type 1 (CB1) receptor pathways. Furthermore, MP-13 did not induce psychological dependence and gastrointestinal motility inhibition at the effective analgesic doses, and it maintained non-tolerance-forming antinociception throughout a 7-day treatment regimen, with an unaltered count of microglial cells in the periaqueductal gray region, supporting this observation. Moreover, intracerebroventricular administration of MP-13 demonstrated dose-dependent antinociception in murine models of neuropathic, inflammatory, and visceral pain. Our findings provide promising insights for the development of opioid/cannabinoid peptide agonists, addressing a crucial gap in the field and holding significant potential for future research and development.

Perspective

This article offers insights into the combination treatment of pepcans with morphiceptin. Among the chimeric peptides, MP-13 exhibited potent analgesic effects in a series of preclinical pain models with a favorable side-effect profile.

Abstract Image

MP-13是一种由吗啡肽和epcan-9组成的新型嵌合肽,可产生强效抗镇痛作用,且副作用有限。
药理学研究证实,双功能阿片/大麻素激动剂在提供强效镇痛的同时可将不良反应降至最低。以前曾对大麻素受体的肽调节剂(称为 pepcans)进行过研究。在这项研究中,我们设计了一系列基于蛋白胨和吗啡肽的嵌合肽(YPFP-NH2)。在此,我们联合注射 pepcans 和 morphiceptin 来研究阿片类药物和大麻的联合治疗,并比较了嵌合化合物的镇痛效果。随后,我们采用计算对接法筛选了针对阿片类和大麻素受体的化合物,并结合急性疼痛模型,找出了最有前景的多肽。在这些多肽中,MP-13(一种吗啡肽和epcan-9 (PVNFKLLSH)构建物)在尾晕试验中表现出卓越的椎上镇痛功效,ED50值为1.43 nmol/只小鼠,优于其母体多肽和其他嵌合类似物。此外,MP-13 还显示出通过μ-阿片受体(MOR)、δ-阿片受体(DOR)和大麻素 1 型(CB1)受体途径介导的强效镇痛活性。此外,在有效镇痛剂量下,MP-13 不会诱发心理依赖和胃肠道蠕动抑制,而且在 7 天的治疗方案中始终保持非耐受性抗痛作用,下uctal 灰色周围区域的小胶质细胞数量也未发生变化,这也支持了这一观察结果。此外,在神经病理性、炎症性和内脏痛的小鼠模型中,MP-13 的脑室内给药显示出剂量依赖性抗痛作用。我们的研究结果为阿片/大麻肽激动剂的开发提供了前景广阔的见解,填补了该领域的一个重要空白,为未来的研究和开发提供了巨大潜力。观点:这篇文章深入探讨了蛋白胨与吗啡肽的联合治疗。在嵌合肽中,MP-13 在一系列临床前疼痛模型中表现出了强大的镇痛效果,而且副作用小。
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来源期刊
Neuropeptides
Neuropeptides 医学-内分泌学与代谢
CiteScore
5.40
自引率
6.90%
发文量
55
审稿时长
>12 weeks
期刊介绍: The aim of Neuropeptides is the rapid publication of original research and review articles, dealing with the structure, distribution, actions and functions of peptides in the central and peripheral nervous systems. The explosion of research activity in this field has led to the identification of numerous naturally occurring endogenous peptides which act as neurotransmitters, neuromodulators, or trophic factors, to mediate nervous system functions. Increasing numbers of non-peptide ligands of neuropeptide receptors have been developed, which act as agonists or antagonists in peptidergic systems. The journal provides a unique opportunity of integrating the many disciplines involved in all neuropeptide research. The journal publishes articles on all aspects of the neuropeptide field, with particular emphasis on gene regulation of peptide expression, peptide receptor subtypes, transgenic and knockout mice with mutations in genes for neuropeptides and peptide receptors, neuroanatomy, physiology, behaviour, neurotrophic factors, preclinical drug evaluation, clinical studies, and clinical trials.
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