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NYX-2925 是一种新型 N-甲基-D-天冬氨酸受体调节剂,可在大鼠神经病理性疼痛模型中诱导快速和持久的镇痛作用。

NYX-2925 Is a Novel -Methyl-d-Aspartate Receptor Modulator that Induces Rapid and Long-Lasting Analgesia in Rat Models of Neuropathic Pain.

机构信息

Aptinyx, Inc., Evanston, Illinois (N.G.-H., J.M.P., J.D.A., E.M.C., J.S.B., M.S.B., C.N.C., M.A.K., J.R.M.) and Falk Center for Molecular Therapeutics, Department of Biomedical Engineering, Northwestern University, Evanston, Illinois (J.S.B., M.S.B., J.R.M.)

Aptinyx, Inc., Evanston, Illinois (N.G.-H., J.M.P., J.D.A., E.M.C., J.S.B., M.S.B., C.N.C., M.A.K., J.R.M.) and Falk Center for Molecular Therapeutics, Department of Biomedical Engineering, Northwestern University, Evanston, Illinois (J.S.B., M.S.B., J.R.M.).

出版信息

J Pharmacol Exp Ther. 2018 Sep;366(3):485-497. doi: 10.1124/jpet.118.249409. Epub 2018 Jul 9.

Abstract

NYX-2925 [(2S,3R)-3-hydroxy-2-((R)-5-isobutyryl-1-oxo-2,5-diazaspiro[3.4]octan-2-yl)butanamide] is a novel -methyl-d-aspartate (NMDA) receptor modulator that is currently being investigated in phase 2 clinical studies for the treatment of painful diabetic peripheral neuropathy and fibromyalgia. Previous studies demonstrated that NYX-2925 is a member of a novel class of NMDA receptor-specific modulators that affect synaptic plasticity processes associated with learning and memory. Studies here examined NYX-2925 administration in rat peripheral chronic constriction nerve injury (CCI) and streptozotocin-induced diabetic mechanical hypersensitivity. Additionally, NYX-2925 was examined in formalin-induced persistent pain model and the tail flick test of acute nociception. Oral administration of NYX-2925 resulted in rapid and long-lasting analgesia in both of the neuropathic pain models and formalin-induced persistent pain, but was ineffective in the tail flick model. The analgesic effects of NYX-2925 were blocked by the systemic administration of NMDA receptor antagonist 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid. Microinjection of NYX-2925 into the medial prefrontal cortex of CCI rats resulted in analgesic effects similar to those observed following systemic administration, whereas intrathecal administration of NYX-2925 was ineffective. In CCI animals, NYX-2925 administration reversed deficits seen in a rat model of rough-and-tumble play. Thus, it appears that NYX-2925 may have therapeutic potential for the treatment of neuropathic pain, and the data presented here support the idea that NYX-2925 may act centrally to ameliorate pain and modulate negative affective states associated with chronic neuropathic pain.

摘要

NYX-2925[(2S,3R)-3-羟基-2-((R)-5-异丁酰基-1-氧代-2,5-二氮杂螺[3.4]辛烷-2-基)丁酰胺]是一种新型的 N-甲基-D-天冬氨酸(NMDA)受体调节剂,目前正在进行 2 期临床试验,用于治疗糖尿病周围神经病理性疼痛和纤维肌痛。先前的研究表明,NYX-2925 是一种新型的 NMDA 受体特异性调节剂,可影响与学习和记忆相关的突触可塑性过程。本研究考察了 NYX-2925 在大鼠周围性慢性缩窄性神经损伤(CCI)和链脲佐菌素诱导的糖尿病机械性超敏中的给药情况。此外,还在福尔马林诱导的持续性疼痛模型和尾部闪烁测试急性痛觉中考察了 NYX-2925。口服 NYX-2925 可迅速且持久地缓解两种神经病理性疼痛模型和福尔马林诱导的持续性疼痛,但在尾部闪烁模型中无效。NMDA 受体拮抗剂 3-(2-羧基哌嗪-4-基)丙基-1-膦酸的全身给药可阻断 NYX-2925 的镇痛作用。CCI 大鼠内侧前额叶皮质内注射 NYX-2925 可产生与全身给药相似的镇痛作用,而鞘内给予 NYX-2925 则无效。在 CCI 动物中,NYX-2925 的给药逆转了翻滚游戏模型中观察到的缺陷。因此,NYX-2925 似乎具有治疗神经病理性疼痛的潜力,本文提供的数据支持 NYX-2925 可能通过中枢作用来改善疼痛和调节与慢性神经病理性疼痛相关的负性情绪状态的观点。

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