4.8 Article

Biodegradable Spheres Protect Traumatically Injured Spinal Cord by Alleviating the Glutamate-Induced Excitotoxicity

期刊

ADVANCED MATERIALS
卷 30, 期 14, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.201706032

关键词

acetalated dextran; alleviated excitotoxicity; calcium ion scavenging; glutamate adsorption; spinal cord injury

资金

  1. Academy of Finland [308742, 252215, 281300]
  2. Jane and Aatos Erkko Foundation [4704010]
  3. HiLIFE Research Funds, Research Funds of the University of Helsinki
  4. European Research Council under the European Union's Seventh Framework Programme (FP) [310892]
  5. National Natural Science Foundation of China [81772352, 81401807, 81772351, 81271988]
  6. Natural Science Foundation of Jiangsu Province [BK2012876]
  7. Academy of Finland (AKA) [308742, 308742] Funding Source: Academy of Finland (AKA)

向作者/读者索取更多资源

New treatment strategies for spinal cord injury with good therapeutic efficacy are actively pursued. Here, acetalated dextran (AcDX), a biodegradable polymer obtained by modifying vicinal diols of dextran, is demonstrated to protect the traumatically injured spinal cord. To facilitate its administration, AcDX is formulated into microspheres (approximate to 7.2 mu m in diameter) by the droplet microfluidic technique. Intrathecally injected AcDX microspheres effectively reduce the traumatic lesion volume and inflammatory response in the injured spinal cord, protect the spinal cord neurons from apoptosis, and ultimately, recover the locomotor function of injured rats. The neuroprotective feature of AcDX microspheres is achieved by sequestering glutamate and calcium ions in cerebrospinal fluid. The scavenging of glutamate and calcium ion reduces the influx of calcium ions into neurons and inhibits the formation of reactive oxygen species. Consequently, AcDX microspheres attenuate the expression of proapoptotic proteins, Calpain, and Bax, and enhance the expression of antiapoptotic protein Bcl-2. Overall, AcDX microspheres protect traumatically injured spinal cord by alleviating the glutamate-induced excitotoxicity. This study opens an exciting perspective toward the application of neuroprotective AcDX for the treatment of severe neurological diseases.

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