Suppr超能文献

纳米星持续释放神经激肽-1 受体拮抗剂,可持久缓解慢性疼痛。

Sustained endosomal release of a neurokinin-1 receptor antagonist from nanostars provides long-lasting relief of chronic pain.

机构信息

Department of Molecular Pathobiology, New York University, New York, 10010, USA; Department of Neuroscience and Physiology, Neuroscience Institute, New York University, New York, 10010, USA.

Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, VIC, 3052, Australia.

出版信息

Biomaterials. 2022 Jun;285:121536. doi: 10.1016/j.biomaterials.2022.121536. Epub 2022 Apr 28.

Abstract

Soft polymer nanoparticles designed to disassemble and release an antagonist of the neurokinin 1 receptor (NKR) in endosomes provide efficacious yet transient relief from chronic pain. These micellar nanoparticles are unstable and rapidly release cargo, which may limit the duration of analgesia. We examined the efficacy of stable star polymer nanostars containing the NKR antagonist aprepitant-amine for the treatment of chronic pain in mice. Nanostars continually released cargo for 24 h, trafficked through the endosomal system, and disrupted NKR endosomal signaling. After intrathecal injection, nanostars accumulated in endosomes of spinal neurons. Nanostar-aprepitant reversed mechanical, thermal and cold allodynia and normalized nociceptive behavior more efficaciously than free aprepitant in preclinical models of neuropathic and inflammatory pain. Analgesia was maintained for >10 h. The sustained endosomal delivery of antagonists from slow-release nanostars provides effective and long-lasting reversal of chronic pain.

摘要

设计用于在内体中解体和释放神经激肽 1 受体 (NKR) 拮抗剂的软聚合物纳米颗粒为慢性疼痛提供了有效但短暂的缓解。这些胶束纳米颗粒不稳定,并且迅速释放货物,这可能会限制镇痛的持续时间。我们研究了含有 NKR 拮抗剂阿瑞匹坦-胺的稳定星形聚合物纳米星用于治疗小鼠慢性疼痛的功效。纳米星持续释放货物 24 小时,通过内体系统运输,并破坏 NKR 内体信号。鞘内注射后,纳米星在脊髓神经元的内体中积累。纳米星-阿瑞匹坦比游离阿瑞匹坦更有效地逆转神经病理性和炎性疼痛的临床前模型中的机械、热和冷感觉过敏,并使痛觉正常化。镇痛作用持续时间超过 10 小时。从缓释纳米星中持续递送来拮抗药可有效且持久地逆转慢性疼痛。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2aa6/10064865/64fd70426bab/nihms-1879621-f0001.jpg

相似文献

引用本文的文献

3
Diabetic neuropathy: cutting-edge research and future directions.糖尿病神经病变:前沿研究与未来方向
Signal Transduct Target Ther. 2025 Apr 25;10(1):132. doi: 10.1038/s41392-025-02175-1.
5
Pain Signaling by GPCRs and RTKs.G蛋白偶联受体(GPCRs)和受体酪氨酸激酶(RTKs)介导的疼痛信号传导
Trends Pharmacol Sci. 2025 Apr;46(4):372-385. doi: 10.1016/j.tips.2025.02.002. Epub 2025 Mar 8.
7
Beneath the surface: endosomal GPCR signaling.表面之下:内体 GPCR 信号转导。
Trends Biochem Sci. 2024 Jun;49(6):520-531. doi: 10.1016/j.tibs.2024.03.006. Epub 2024 Apr 19.

本文引用的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验