Mettyas Tamer, Barton Matthew, Sahar Muhammad Sana Ullah, Lawrence Felicity, Sanchez-Herrero Alvaro, Shah Megha, St John James, Bindra Randy
Department of Orthopaedics, Queen Elizabeth II Hospital, Brisbane, Queensland, Australia.
School of Nursing and Midwifery, Griffith University, Australia.
Plast Reconstr Surg Glob Open. 2021 May 13;9(5):e3568. doi: 10.1097/GOX.0000000000003568. eCollection 2021 May.
Various modalities to facilitate nerve regeneration have been described in the literature with limited success. We hypothesized that negative pressure applied to a sectioned peripheral nerve would enhance nerve regeneration by promoting angiogenesis and axonal lengthening.
Wistar rats' sciatic nerves were cut (creating ~7 mm nerve gap) and placed into a silicone T-tube, to which negative pressure was applied. The rats were divided into 4 groups: control (no pressure), group A (low pressure: 10 mm Hg), group B (medium pressure: 20/30 mm Hg) and group C (high pressure: 50/70 mm Hg). The nerve segments were retrieved after 7 days for gross and histological analysis.
In total, 22 rats completed the study. The control group showed insignificant nerve growth, whereas the 3 negative pressure groups showed nerve growth and nerve gap reduction. The true nerve growth was highest in group A (median: 3.54 mm) compared to group B, C, and control (medians: 1.19 mm, 1.3 mm, and 0.35 mm); however, only group A was found to be significantly different to the control group (** < 0.01). Similarly, angiogenesis was observed to be significantly greater in group A (** < 0.01) in comparison to the control.
Negative pressure stimulated nerve lengthening and angiogenesis within an in vivo rat model. Low negative pressure (10 mm Hg) provided superior results over the higher negative pressure groups and the control, favoring axonal growth. Further studies are required with greater number of rats and longer recovery time to assess the functional outcome.
文献中描述了多种促进神经再生的方法,但成效有限。我们推测,对切断的周围神经施加负压可通过促进血管生成和轴突延长来增强神经再生。
切断Wistar大鼠的坐骨神经(造成约7毫米的神经间隙),将其置于硅胶T形管中,并对其施加负压。将大鼠分为4组:对照组(无压力)、A组(低压:10毫米汞柱)、B组(中压:20/30毫米汞柱)和C组(高压:50/70毫米汞柱)。7天后取出神经段进行大体和组织学分析。
共有22只大鼠完成了该研究。对照组神经生长不明显,而3个负压组均有神经生长且神经间隙减小。与B组、C组和对照组(中位数分别为1.19毫米、1.3毫米和0.35毫米)相比,A组的真正神经生长最高(中位数:3.54毫米);然而,仅A组与对照组有显著差异(**P<0.01)。同样,与对照组相比,A组的血管生成也明显更显著(**P<0.01)。
负压刺激了体内大鼠模型中的神经延长和血管生成。低负压(10毫米汞柱)比高负压组和对照组效果更好,有利于轴突生长。需要更多大鼠和更长恢复时间的进一步研究来评估功能结果。