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载罗匹司特的 PgP 纳米颗粒减少大鼠中度挫伤性 SCI 模型的继发性损伤并增强运动功能恢复。

Rolipram-loaded PgP nanoparticle reduces secondary injury and enhances motor function recovery in a rat moderate contusion SCI model.

机构信息

Drug Design Delivery and Development (4D) Laboratory, Department of Bioengineering, Clemson University, Clemson, SC, USA.

Drug Design Delivery and Development (4D) Laboratory, Department of Bioengineering, Clemson University, Clemson, SC, USA.

出版信息

Nanomedicine. 2023 Sep;53:102702. doi: 10.1016/j.nano.2023.102702. Epub 2023 Aug 11.

Abstract

Spinal cord injury (SCI) results in immediate axonal damage and cell death, as well as a prolonged secondary injury consist of a cascade of pathophysiological processes. One important aspect of secondary injury is activation of phosphodiesterase 4 (PDE4) that leads to reduce cAMP levels in the injured spinal cord. We have developed an amphiphilic copolymer, poly (lactide-co-glycolide)-graft-polyethylenimine (PgP) that can deliver Rolipram, the PDE4 inhibitor. The objective of this work was to investigate the effect of rolipram loaded PgP (Rm-PgP) on secondary injury and motor functional recovery in a rat moderate contusion SCI model. We observed that Rm-PgP can increase cAMP level at the lesion site, and reduce secondary injury such as the inflammatory response by macrophages/microglia, astrogliosis by activated astrocytes and apoptosis as well as improve neuronal survival at 4 weeks post-injury (WPI). We also observed that Rm-PgP can improve motor functional recovery after SCI over 4 WPI.

摘要

脊髓损伤 (SCI) 会导致轴突立即损伤和细胞死亡,以及持续的继发性损伤,包括一系列病理生理过程。继发性损伤的一个重要方面是磷酸二酯酶 4 (PDE4) 的激活,这会导致损伤脊髓中环腺苷酸 (cAMP) 水平降低。我们开发了一种两亲性共聚物,聚 (乳酸-共-乙醇酸)-接枝-聚乙烯亚胺 (PgP),可以递送罗利普兰,即 PDE4 抑制剂。这项工作的目的是研究载有罗利普兰的 PgP (Rm-PgP) 在大鼠中度挫伤性 SCI 模型中的继发性损伤和运动功能恢复的影响。我们观察到,Rm-PgP 可以增加损伤部位的 cAMP 水平,并减轻继发性损伤,如巨噬细胞/小胶质细胞的炎症反应、激活的星形胶质细胞的星形胶质化以及神经元凋亡,以及在损伤后 4 周 (WPI) 时提高神经元存活率。我们还观察到,Rm-PgP 可以改善 SCI 后 4 周以上的运动功能恢复。

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