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大鼠正中神经拉伸损伤时机械和结构破坏的顺序是怎样的?神经断裂分类。

What Is the Sequence of Mechanical and Structural Failure During Stretch Injury in the Rat Median Nerve? The Neuroclasis Classification.

作者信息

Schroen Christoph A, Duey Akiro H, Nasser Philip, Laudier Damien, Cagle Paul J, Hausman Michael R

机构信息

Leni & Peter W. May Department of Orthopaedic Surgery, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Department of Hand, Plastic and Reconstructive Surgery, Burn Center, BG Trauma Center Ludwigshafen, Ludwigshafen, Germany.

出版信息

Clin Orthop Relat Res. 2025 Jun 1;483(6):1142-1158. doi: 10.1097/CORR.0000000000003405. Epub 2025 Feb 18.

Abstract

BACKGROUND

Peripheral nerve injury commonly results in long-term disability and pain for patients. Recovery after nerve traction or crush injury is unpredictable and depends on the degree of injury. Our inability to accurately assess the severity or degree of injury hampers our ability to predict the chances for recovery or need for surgical intervention in the form of neurolysis, nerve repair, or nerve graft. An investigation into the histologic sequence and mechanics of nerve failure under tension may help in the process of accurately assessing the severity of the nerve injury, the prognosis for recovery, and the need for surgical treatment.

QUESTIONS/PURPOSES: Using an in vivo rat model, we asked: (1) What is the pattern of mechanical failure during nerve stretch? (2) Is there staggered disintegration of specific anatomic substructures when mechanical failure occurs?

METHODS

To answer our first research question about the pattern of mechanical failure during nerve stretch, four 12-month-old male Sprague-Dawley rats were enrolled in a load-to-failure experiment generating load-deformation curves of the rat median nerve. Under anesthesia, the median nerves of both forelimbs were surgically exposed and secured under two blunt metal pins 1 cm apart. A metal hook was attached to a load-cell and raised from beneath the nerve at a speed of 0.2 mm/second until complete rupture occurred. Applied forces were monitored in real time via a force-time curve. All experiments were filmed, and the rats were euthanized afterward. Based on load-to-failure experiments, we identified two distinct events of sudden force reduction during stretching in the load-deformation curve of the rat median nerve. We labeled the first of these two events as epineuroclasis and the second as endoneuroclasis. Neuroclasis derives from the Greek term "neuron" for nerve, and the suffix "-clasis" means breaking or fracture. An additional eight rats were used to investigate whether this staggered mechanical failure was caused by staggered disintegration of specific anatomical substructures. Under anesthesia, eight left median nerves were stretched to the epineuroclasis point and eight right nerves to the endoneuroclasis point. Induction of injury was confirmed by load-time curves, and nerves were held in place for 5 minutes before tension was released. Nerve function was assessed before and after injury using a handheld electrical nerve stimulator. The nerves were harvested for histology (to assess integrity of the epineurium, axons and intraneural vasculature, endoneurial collagen [dis-]organization, as well as molecular collagen damage), and the rats were euthanized immediately after. The uninjured median nerves of two additional rats were harvested for histology as control tissue. Mechanical, functional, and histologic findings were compared between both injury levels and with uninjured nerves.

RESULTS

Load-to-failure experiments revealed a characteristic failure pattern of the rat median nerve with two distinct events of mechanical failure that occurred at a mean ± SD resistance force of 2.3 ± 0.5 N and 1.4 ± 0.2 N (mean difference 0.9 ± 0.6 N [95% confidence interval 0.4 to 1.4]; p = 0.003), respectively. Additional experiments investigating both mechanical failure points revealed that the first failure point (epineuroclasis) was associated with epineurium rupture and plastic deformation of nerve fibers, whereas the second injury point (endoneuroclasis) was associated with failure of endoneurial tubes, axons, and intraneural vasculature. Epineuroclasis severely impaired nerve conductivity (median stimulation of 25 nC [range 25 nC to 50 nC] preinjury and 170 nC [range 25 to 300 nC] after epineuroclasis, difference of medians 145 nC; p < 0.001). Endoneuroclasis induced an even greater functional impairment than epineuroclasis (median stimulation of 400 nC [range 300 to 2000 nC] after endoneuroclasis, difference of medians 230 nC; p = 0.005). Both injury levels could be induced through live analysis of resistance forces during nerve stretch.

CONCLUSION

Peripheral nerve injuries follow a characteristic sequence of mechanical and structural failure, with two distinct injury levels preceding nerve transection.

CLINICAL RELEVANCE

The order and degree of failure in the rat median nerve seems to follow a predictable "outside-in" pattern. This sequence of mechanical and structural failure may inform a classification system of nerve stretch injuries that may more accurately reflect the pathoanatomy and prognosis. We offer a new classification of nerve injuries based on the sequence of nerve failure in rats. However, future studies are needed to validate the applicability of the neuroclasis classification to human peripheral nerves before clinical implementation and use can be proposed. The characterization of specific injury levels using an animal model provides a framework that could facilitate the development of novel diagnostic tools, potentially identifying the specific structural changes found in this study in the acute clinical setting.

摘要

背景

周围神经损伤常给患者带来长期残疾和疼痛。神经牵拉或挤压伤后的恢复情况难以预测,且取决于损伤程度。我们无法准确评估损伤的严重程度阻碍了我们预测恢复几率或判断是否需要进行神经松解、神经修复或神经移植等手术干预的能力。对神经在张力下衰竭的组织学序列和力学进行研究,可能有助于准确评估神经损伤的严重程度、恢复预后以及手术治疗的必要性。

问题/目的:我们使用大鼠体内模型,提出以下问题:(1)神经拉伸过程中的机械性衰竭模式是怎样的?(2)机械性衰竭发生时,特定解剖亚结构是否会出现交错性崩解?

方法

为回答关于神经拉伸过程中机械性衰竭模式的首个研究问题,选取4只12月龄雄性Sprague-Dawley大鼠进行负荷至衰竭实验,生成大鼠正中神经的负荷-变形曲线。在麻醉状态下,手术暴露双前肢的正中神经,并固定于两根相距1 cm的钝性金属针之间。将一个金属钩连接到测力传感器上,以0.2 mm/秒的速度从神经下方升起,直至完全断裂。通过力-时间曲线实时监测施加的力。所有实验均进行拍摄,之后对大鼠实施安乐死。基于负荷至衰竭实验,我们在大鼠正中神经的负荷-变形曲线中识别出拉伸过程中两个明显的力突然降低事件。我们将这两个事件中的第一个标记为神经外膜破裂,第二个标记为神经内膜破裂。Neuroclasis一词源于希腊语“neuron”(意为神经),后缀“-clasis”表示断裂或骨折。另外使用8只大鼠研究这种交错性机械性衰竭是否由特定解剖亚结构的交错性崩解引起。在麻醉状态下,将8只大鼠的左侧正中神经拉伸至神经外膜破裂点,8只大鼠的右侧正中神经拉伸至神经内膜破裂点。通过负荷-时间曲线确认损伤诱导情况,在释放张力前将神经固定在位5分钟。使用手持式电神经刺激器在损伤前后评估神经功能。采集神经进行组织学检查(评估神经外膜、轴突和神经内血管的完整性、神经内膜胶原的[非]组织化以及分子胶原损伤),之后立即对大鼠实施安乐死。另外选取2只大鼠的未损伤正中神经作为对照组织进行组织学检查。比较两种损伤水平与未损伤神经之间的力学、功能和组织学结果。

结果

负荷至衰竭实验揭示了大鼠正中神经的特征性衰竭模式,有两个明显的机械性衰竭事件,分别发生在平均±标准差阻力为2.3±0.5 N和1.4±0.2 N(平均差值0.9±0.6 N[95%置信区间0.4至1.4];p = 0.003)时。对两个机械性衰竭点进行的额外实验表明,第一个衰竭点(神经外膜破裂)与神经外膜破裂和神经纤维的塑性变形有关,而第二个损伤点(神经内膜破裂)与神经内膜管、轴突和神经内血管的衰竭有关。神经外膜破裂严重损害神经传导性(损伤前中位刺激量为25 nC[范围25 nC至50 nC],神经外膜破裂后为170 nC[范围25至300 nC],中位数差值为145 nC;p < 0.001)。神经内膜破裂比神经外膜破裂诱导的功能损害更大(神经内膜破裂后中位刺激量为400 nC[范围300至2000 nC],中位数差值为2

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