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布洛芬和吲哚美辛在促进周围神经再生中的双重作用

Dual Role of Ibuprofen and Indomethacin in Promoting Peripheral Nerve Regeneration .

作者信息

Tusnim Jarin, Pfister Bryan J, Grasman Jonathan M

机构信息

Department of Biomedical Engineering, New Jersey Institute of Technology, Newark, New Jersey, USA.

出版信息

Tissue Eng Part A. 2025 Jul;31(13-14):1026-1037. doi: 10.1089/ten.tea.2024.0224. Epub 2024 Oct 24.

DOI:10.1089/ten.tea.2024.0224
PMID:39446790
Abstract

Peripheral nerve injuries (PNI) can result in significant losses of motor and sensory function. Although peripheral nerves have an innate capacity for regeneration, restoration of function after severe injury remains suboptimal. The gold standard for peripheral nerve regeneration (PNR) is autologous nerve transplantation, but this method is limited by the generation of an additional surgical site, donor-site morbidity, and neuroma formation at the site of harvest. Although targeted drug compounds have the potential to influence axonal growth, there are no drugs currently approved to treat PNI. Therefore, we propose to repurpose commonly used nonsteroidal anti-inflammatory drugs (NSAIDs) to enhance PNR, facilitating easier clinical translation. Additionally, calcium signaling plays a crucial role in neuronal connectivity and regeneration, but how specific drugs modulate this process remains unclear. We developed an hollow channel collagen gel platform that successfully supports neuronal network formation. This study evaluated the effects of commonly used NSAIDs, namely ibuprofen and indomethacin, in our model of axonal growth, regeneration, and calcium signaling as potential treatments for PNI. Our results demonstrate enhanced axonal growth and regrowth with both ibuprofen and indomethacin, suggesting a positive influence on PNR. Further, these drugs showed enhanced calcium signaling dynamics, which we posit is a crucial aspect for nerve repair. Taken together, these findings highlight the potential of ibuprofen and indomethacin to be used as treatment options for PNI, given their dual capability to promote axonal growth and enhance calcium signaling.

摘要

周围神经损伤(PNI)可导致运动和感觉功能的显著丧失。尽管周围神经具有天生的再生能力,但严重损伤后的功能恢复仍不尽人意。周围神经再生(PNR)的金标准是自体神经移植,但这种方法受到额外手术部位的产生、供体部位并发症以及取材部位神经瘤形成的限制。尽管靶向药物化合物有可能影响轴突生长,但目前尚无获批用于治疗PNI的药物。因此,我们提议重新利用常用的非甾体抗炎药(NSAIDs)来促进PNR,以便于临床转化。此外,钙信号在神经元连接和再生中起着关键作用,但具体药物如何调节这一过程仍不清楚。我们开发了一种中空通道胶原凝胶平台,该平台成功支持神经元网络的形成。本研究评估了常用的NSAIDs,即布洛芬和吲哚美辛,在我们的轴突生长、再生和钙信号模型中作为PNI潜在治疗方法的效果。我们的结果表明,布洛芬和吲哚美辛均可增强轴突生长和再生长,提示对PNR有积极影响。此外,这些药物显示出增强的钙信号动力学,我们认为这是神经修复的一个关键方面。综上所述,鉴于布洛芬和吲哚美辛具有促进轴突生长和增强钙信号的双重能力,这些发现突出了它们作为PNI治疗选择的潜力。

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