Facial-nerve regeneration ability of a hybrid artificial nerve conduit containing uncultured adipose-derived stromal vascular fraction: An experimental study.
Matsumine H., Numakura K., Climov M., Watanabe Y., Giatsidis G., Orgill DP.
Animal Study with a reported sample of 30 on Face & Skin, published in Microsurgery (2016) — summary generated from the PubMed abstract.
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
- Level A · Stronger Clinical Evidence
- Level B · Emerging clinical evidence with positive signals
- Level C · Early human research exploring benefits
- Level D · Scientific groundwork from lab and animal studies
- Emerging · Emerging topic under active research
This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.
- Study type
- Animal Study
- Journal
- Microsurgery (2016)
- Country
- United States
- Reported sample size
- 30
- Source database
- PubMed
- PMID
- 27273726
- DOI
- 10.1002/micr.30060
- Citations
- 19
Abstract (original English)
This study investigated the potential of uncultured-stromal-vascular-fraction (SVF) cells in promoting facial nerve regeneration in a rat model. A 7-mm nerve defect was created in the buccal branch of facial nerve in five groups of Lewis rats (total n = 30, n = 6 per group). A silicone tube, infused with syngeneic uncultured-SVF was implanted into the facial nerve defect. Groups 1-3 received 1 × 10 3 , 1 × 10 5 , and 1 × 10 7 cells, and regenerated nerves were examined at 13 weeks after the surgery. The findings were compared to the autograft and collagen-alone groups with facial palsy score (FPS), the number of myelinated fibers, fiber diameter, axon diameter, myelin thickness, and g ratio. There was no significant difference in FPS between the autograft and 1 × 10 5 -cell groups at 13 weeks after surgery, and FPS values of these two groups were significantly higher than those of the other three groups (P < 0.01). Axon diameter significantly increased in the 1 × 10 5 -cell group compared with the 1 × 10 3 - (P < 0.05) and 1 × 10 7 -cell groups (P < 0.01). Myelin thickness was found to be the highest in the autograft group, followed by the 1 × 10 5 -, 1 × 10 3 -, 1 × 10 7 -cell, and negative control groups, and there were significant differences among all groups (P < 0.01). The infusion of uncultured-SVF into the artificial nerve conduit promoted optimal nerve regeneration that
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is preclinical work; animal or laboratory results cannot be applied to humans.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
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