4.5 Article

Single-Walled Carbon Nanotubes Chemically Functionalized with Polyethylene Glycol Promote Tissue Repair in a Rat Model of Spinal Cord Injury

期刊

JOURNAL OF NEUROTRAUMA
卷 28, 期 11, 页码 2349-2362

出版社

MARY ANN LIEBERT INC
DOI: 10.1089/neu.2010.1409

关键词

axonal regeneration; gliosis; graft; nanofibers; nanomaterials

资金

  1. UAB BioMatrix Engineering and Regenerative Medicine (BERM) Center
  2. Center for Glial Biology in Medicine
  3. Department of Physical Medicine and Rehabilitation
  4. Ronald E. McNair Post-Baccalaureate Achievement Program
  5. Wachovia Scholars Foundation
  6. National Institute of Mental Health [R01 MH 069791]
  7. National Science Foundation [CBET 0943343]
  8. National Institutes of Health
  9. Div Of Chem, Bioeng, Env, & Transp Sys
  10. Directorate For Engineering [943343] Funding Source: National Science Foundation

向作者/读者索取更多资源

Traumatic spinal cord injury (SCI) induces tissue damage and results in the formation of a cavity that inhibits axonal regrowth. Filling this cavity with a growth-permissive substrate would likely promote regeneration and repair. Single-walled carbon nanotubes functionalized with polyethylene glycol (SWNT-PEG) have been shown to increase the length of selected neurites in vitro. We hypothesized that administration of SWNT-PEG after experimental SCI will promote regeneration of axons into the lesion cavity and functional recovery of the hindlimbs. To evaluate this hypothesis, complete transection SCI was induced at the T9 vertebral level in adult female rats. One week after transection, the epicenter of the lesion was injected with 25 mu L of either vehicle (saline), or 1 mu g/mL, 10 mu g/mL, or 100 mu g/mL of SWNT-PEG. Behavioral analysis was conducted before injury, before treatment, and once every 7 days for 28 days after treatment. At 28 days post-injection the rats were euthanized and spinal cord tissue was extracted. Immunohistochemistry was used to detect the area of the cyst, the extent of the glial scar, and axonal morphology. We found that post-SCI administration of SWNT-PEG decreased lesion volume, increased neurofilament-positive fibers and corticospinal tract fibers in the lesion, and did not increase reactive gliosis. Additionally, post-SCI administration of SWNT-PEG induced a modest improvement in hindlimb locomotor recovery without inducing hyperalgesia. These data suggest that SWNT-PEG may be an effective material to promote axonal repair and regeneration after SCI.

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