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聚乙醇酸导管神经端封闭治疗大鼠坐骨神经瘤:初步报告。

Nerve-End Capping Treatment with a Polyglycolic Acid Conduit for Rat Sciatic Neuroma: A Preliminary Report.

机构信息

Department of Orthopaedic Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan.

Department of Orthopaedic Surgery, Osaka General Hospital of West Japan Railway Company, Osaka, Japan.

出版信息

J Reconstr Microsurg. 2022 Nov;38(9):711-720. doi: 10.1055/s-0042-1757208. Epub 2022 Sep 19.

Abstract

BACKGROUND

The treatment of painful neuroma remains challenging. Recently, a nerve-end capping technique using a bioabsorbable nerve conduit was newly introduced to treat amputation neuroma. A collagen-coated polyglycolic acid (PGA) conduit has been commercially available for the reconstruction of peripheral nerve defects, yielding successful clinical outcomes. However, no experimental research has been conducted using this PGA nerve conduit as capping device for treating amputation neuroma. The purpose of this study was to investigate nerve-end capping treatment with the PGA conduit in the rat sciatic nerve amputation model, focusing on histological scar formation and neuroinflammation.

METHODS

Forty-seven rats were divided into two groups: no capping (transected nerve stump without capping;  = 25) and capping (nerve-end capping with collagen-coated PGA nerve conduit;  = 22). Twelve weeks after sciatic neurectomy, neuropathic pain was evaluated using the autotomy score. Stump neuromas were histologically evaluated or perineural scar and neuroinflammation.

RESULTS

While autotomy scores gradually exacerbated in both groups, they were consistently lower in the capping group at 4, 8, and 12 weeks postprocedure. Twelve weeks after surgery, the transected nerve stumps in the no-capping group had formed macroscopic bulbous neuromas strongly adhering to surrounding tissues, whereas they remained wrapped with the PGA nerve conduits loosely adhering to surrounding tissues in the capping group. Histologically, distal axonal fibers were expanded radially and formed neuromas in the no-capping group, while they were terminated within the PGA conduit in the capping group. Perineural scars and neuroinflammation were widely found surrounding the randomly sprouting nerve end in the no-capping group. In capped counterparts, scars and inflammation were limited to closely around the terminated nerve end.

CONCLUSION

Nerve-end capping with a collagen-coated PGA conduit after rat sciatic neurectomy might prevent neuroma formation by suppressing perineural scar formation and neuroinflammation around the nerve stump, potentially relieving neuropathic pain.

摘要

背景

治疗疼痛性神经瘤仍然具有挑战性。最近,一种使用可吸收神经导管的神经末梢封闭技术被新引入用于治疗截肢神经瘤。一种胶原蛋白涂层的聚乙二醇酸(PGA)导管已可用于周围神经缺损的重建,并取得了成功的临床效果。然而,尚未有实验研究使用这种 PGA 神经导管作为治疗截肢神经瘤的封闭装置。本研究旨在探讨 PGA 导管在大鼠坐骨神经切断模型中的神经末梢封闭治疗作用,重点关注组织学瘢痕形成和神经炎症。

方法

47 只大鼠分为两组:无封闭(未封闭的神经断端;=25)和封闭(用胶原蛋白涂层 PGA 神经导管进行神经末梢封闭;=22)。坐骨神经切断后 12 周,使用自截评分评估神经病理性疼痛。对残端神经瘤进行组织学评估或神经外膜瘢痕和神经炎症评估。

结果

虽然两组的自截评分都逐渐加重,但在术后 4、8 和 12 周时,封闭组的评分始终较低。术后 12 周,无封闭组的神经断端形成了明显的大球状神经瘤,与周围组织强烈粘连,而封闭组的神经瘤仍被 PGA 神经导管松散包裹,与周围组织粘连。组织学上,无封闭组的远端轴突纤维呈放射状扩张并形成神经瘤,而封闭组的远端轴突纤维则在 PGA 导管内终止。无封闭组的神经末梢随机长出的神经周围有广泛的神经外膜瘢痕和神经炎症。在封闭组的对应物中,瘢痕和炎症局限于神经末端终止处周围。

结论

大鼠坐骨神经切断后用胶原蛋白涂层 PGA 导管进行神经末梢封闭可能通过抑制神经断端周围的神经外膜瘢痕形成和神经炎症来防止神经瘤形成,从而可能缓解神经病理性疼痛。

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