Biodegradable Spheres Protect Traumatically Injured Spinal Cord by Alleviating the Glutamate-Induced Excitotoxicity.
Dongfei LiuJian ChenTao JiangWei LiYao HuangXiyi LuZehua LiuWeixia ZhangZheng ZhouQirui DingHélder A SantosGuoyong YinJin FanPublished in: Advanced materials (Deerfield Beach, Fla.) (2018)
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 (≈7.2 µm 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.
Keyphrases
- spinal cord
- spinal cord injury
- neuropathic pain
- inflammatory response
- poor prognosis
- molecularly imprinted
- reactive oxygen species
- cerebrospinal fluid
- high glucose
- drug delivery
- machine learning
- binding protein
- high throughput
- cerebral ischemia
- quantum dots
- single cell
- cell death
- early onset
- long non coding rna
- brain injury
- toll like receptor
- subarachnoid hemorrhage
- high resolution
- circulating tumor cells
- amino acid
- protein protein