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脊髓损伤中神经胶质细胞的协同药物调节治疗

Synergistic Pharmacological Therapy to Modulate Glial Cells in Spinal Cord Injury.

机构信息

Department of Neuroscience, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, via Mario Negri 2, Milano, 20156, Italy.

Faculty of Biomedical Sciences, Università della Svizzera Italiana, via Buffi 13, Lugano, 6900, Switzerland.

出版信息

Adv Mater. 2024 Jan;36(3):e2307747. doi: 10.1002/adma.202307747. Epub 2023 Dec 2.

Abstract

Current treatments for modulating the glial-mediated inflammatory response after spinal cord injury (SCI) have limited ability to improve recovery. This is quite likely due to the lack of a selective therapeutic approach acting on microgliosis and astrocytosis, the glia components most involved after trauma, while maximizing efficacy and minimizing side effects. A new nanogel that can selectively release active compounds in microglial cells and astrocytes is developed and characterized. The degree of selectivity and subcellular distribution of the nanogel is evaluated by applying an innovative super-resolution microscopy technique, expansion microscopy. Two different administration schemes are then tested in a SCI mouse model: in an early phase, the nanogel loaded with Rolipram, an anti-inflammatory drug, achieves significant improvement in the animal's motor performance due to the increased recruitment of microglia and macrophages that are able to localize the lesion. Treatment in the late phase, however, gives opposite results, with worse motor recovery because of the widespread degeneration. These findings demonstrate that the nanovector can be selective and functional in the treatment of the glial component in different phases of SCI. They also open a new therapeutic scenario for tackling glia-mediated inflammation after neurodegenerative events in the central nervous system.

摘要

目前用于调节脊髓损伤 (SCI) 后神经胶质介导的炎症反应的治疗方法,其改善恢复的能力有限。这很可能是由于缺乏针对创伤后最相关的小胶质细胞和星形胶质细胞的选择性治疗方法,同时最大限度地提高疗效和最小化副作用。开发并表征了一种新的纳米凝胶,该纳米凝胶可以选择性地在小胶质细胞和星形胶质细胞中释放活性化合物。通过应用创新的超分辨率显微镜技术——扩展显微镜,评估了纳米凝胶的选择性和亚细胞分布程度。然后在 SCI 小鼠模型中测试了两种不同的给药方案:在早期阶段,负载罗利普兰(一种抗炎药物)的纳米凝胶由于募集了能够定位病变的小胶质细胞和巨噬细胞,从而显著改善了动物的运动性能。然而,在晚期阶段进行治疗会产生相反的结果,因为广泛的退行性变导致运动恢复更差。这些发现表明,纳米载体在 SCI 的不同阶段针对神经胶质成分的治疗中具有选择性和功能性。它们还为中枢神经系统神经退行性事件后针对神经胶质介导的炎症开辟了新的治疗方案。

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