The Effects of Intraoperative Electrical Stimulation on Regeneration and Recovery After Nerve Isograft Repair in a Rat Model

被引:16
|
作者
Keane, Grace C. [1 ]
Pan, Deng [1 ]
Roh, Joseph [1 ]
Larson, Ellen L. [1 ]
Schellhardt, Lauren [1 ]
Hunter, Daniel A. [1 ]
Snyder-Warwick, Alison K. [1 ]
Moore, Amy M. [2 ]
Mackinnon, Susan E. [1 ]
Wood, Matthew D. [1 ,3 ]
机构
[1] Washington Univ St Louis, St Louis, MO USA
[2] Ohio State Univ, Columbus, OH USA
[3] Washington Univ St Louis, Sch Med, Dept Surg, Div Plast & Reconstruct Surg, Campus Box 8238,660 South Euclid Ave, St Louis, MO 63110 USA
来源
HAND-AMERICAN ASSOCIATION FOR HAND SURGERY | 2022年 / 17卷 / 03期
基金
美国国家卫生研究院;
关键词
nerve; basic science; autograft; muscle; nerve regeneration; diagnosis; microsurgery; specialty; ACCELERATES AXON REGENERATION; POOR FUNCTIONAL RECOVERY; CONTRIBUTING FACTORS; PROMOTES; PATHWAYS; SPEED;
D O I
10.1177/1558944720939200
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background: Therapeutic electrical stimulation (ES) applied to repaired nerve is a promising treatment option to improve regeneration. However, few studies address the impact of ES following nerve graft reconstruction. The purpose of this study was to determine if ES applied to a nerve repair using nerve isograft in a rodent model could improve nerve regeneration and functional recovery. Methods: Adult rats were randomized to 2 groups: "ES" and "Control." Rats received a tibial nerve transection that was repaired using a tibial nerve isograft (1.0 cm length), where ES was applied immediately after repair in the applicable group. Nerve was harvested 2 weeks postrepair for immunohistochemical analysis of axon growth and macrophage accumulation. Independently, rats were assessed using walking track and grid-walk analysis for up to 21 weeks. Results: At 2 weeks, more robust axon regeneration and greater macrophage accumulation was observed within the isografts for the ES compared to Control groups. Both walking track and grid-walk analysis revealed that return of functional recovery was accelerated by ES. The ES group demonstrated improved functional recovery over time, as well as improved recovery compared to the Control group at 21 weeks. Conclusions: ES improved early axon regeneration into a nerve isograft and was associated with increased macrophage and beneficial M2 macrophage accumulation within the isograft. ES ultimately improved functional recovery compared to isograft repair alone. This study supports the clinical potential of ES to improve the management of nerve injuries requiring a nerve graft repair.
引用
收藏
页码:540 / 548
页数:9
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