4.3 Article

Role of timing in assessment of nerve regeneration

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MICROSURGERY
卷 28, 期 4, 页码 265-272

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WILEY-LISS
DOI: 10.1002/micr.20483

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  1. NIDCD NIH HHS [T32 DC 0022-15, T32 DC000022] Funding Source: Medline
  2. NINDS NIH HHS [R01 NS033406, 2R01 NS33406-12] Funding Source: Medline
  3. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS033406] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS [T32DC000022] Funding Source: NIH RePORTER

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Small animal models are indispensable for research on nerve injury and reconstruction, but their superlative regenerative potential may confound experimental interpretation. This study investigated time-dependent neuroregenerative phenomena in rodents. Forty-six Lewis rats were randomized to three nerve allograft groups treated with 2 mg/(kg day) tacrolimus; 5 mg/(kg day) Cyclosporine A; or placebo injection. Nerves were subjected to histomorphometric and walking track analysis at serial time points. Tacrolimus increased fiber density, percent neural tissue, and nerve fiber count and accelerated functional recovery at 40 days, but these differences were undetectable by 70 days. Serial walking track analysis showed a similar pattern of recovery. A 'blow-through' effect is observed in rodents whereby an advancing nerve front overcomes an experimental defect given sufficient time, rendering experimental groups indistinguishable at late time points. Selection of validated time points and corroboration in higher animal models are essential prerequisites for the clinical application of basic research on nerve regeneration. (c) 2008 Wiley-Liss, Inc.

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