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小鼠模型中新生儿臂丛神经损伤后的传入神经支配、肌梭与挛缩

Afferent Innervation, Muscle Spindles, and Contractures Following Neonatal Brachial Plexus Injury in a Mouse Model.

作者信息

Nikolaou Sia, Hu Liangjun, Cornwall Roger

机构信息

Division of Orthopaedic Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.

Division of Orthopaedic Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, OH; Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.

出版信息

J Hand Surg Am. 2015 Oct;40(10):2007-16. doi: 10.1016/j.jhsa.2015.07.008. Epub 2015 Aug 28.

Abstract

PURPOSE

We used an established mouse model of elbow flexion contracture after neonatal brachial plexus injury (NBPI) to test the hypothesis that preservation of afferent innervation protects against contractures and is associated with preservation of muscle spindles and ErbB signaling.

METHODS

A model of preganglionic C5 through C7 NBPI was first tested in mice with fluorescent axons using confocal imaging to confirm preserved afferent innervation of spindles despite motor end plate denervation. Preganglionic and postganglionic injuries were then created in wild-type mice. Four weeks later, we assessed total and afferent denervation of the elbow flexors by musculocutaneous nerve immunohistochemistry. Biceps muscle volume and cross-sectional area were measured by micro computed tomography. An observer who was blinded to the study protocol measured elbow flexion contractures. Biceps spindle and muscle fiber morphology and ErbB signaling pathway activity were assessed histologically and immunohistochemically.

RESULTS

Preganglionic and postganglionic injuries caused similar total denervation and biceps muscle atrophy. However, after preganglionic injuries, afferent innervation was partially preserved and elbow flexion contractures were significantly less severe. Spindles degenerated after postganglionic injury but were preserved after preganglionic injury. ErbB signaling was inactivated in denervated spindles after postganglionic injury but ErbB signaling activity was preserved in spindles after preganglionic injury with retained afferent innervation. Preganglionic and postganglionic injuries were associated with upregulation of ErbB signaling in extrafusal muscle fibers.

CONCLUSIONS

Contractures after NBPI are associated with muscle spindle degeneration and loss of spindle ErbB signaling activity. Preservation of afferent innervation maintained spindle development and ErbB signaling activity, and protected against contractures.

CLINICAL RELEVANCE

Pharmacologic modulation of ErbB signaling, which is being investigated as a therapy for congestive heart failure, may be able to recapitulate the protective effects of afferent innervation in spindle development and contracture prevention. Muscle spindle preservation may also have implications in proprioception and motor learning, both of which are impaired in NBPI.

摘要

目的

我们使用一种已建立的新生儿臂丛神经损伤(NBPI)后肘关节屈曲挛缩的小鼠模型,来检验以下假设:保留传入神经支配可预防挛缩,且与肌梭和表皮生长因子受体(ErbB)信号通路的保留有关。

方法

首先在具有荧光轴突的小鼠中测试节前C5至C7 NBPI模型,使用共聚焦成像来确认尽管运动终板去神经支配,但肌梭的传入神经支配得以保留。然后在野生型小鼠中造成节前和节后损伤。四周后,我们通过肌皮神经免疫组织化学评估肘屈肌的完全去神经支配和传入神经去神经支配情况。通过微型计算机断层扫描测量肱二头肌体积和横截面积。一名对研究方案不知情的观察者测量肘关节屈曲挛缩情况。通过组织学和免疫组织化学评估肱二头肌肌梭和肌纤维形态以及ErbB信号通路活性。

结果

节前和节后损伤导致相似程度的完全去神经支配和肱二头肌萎缩。然而,节前损伤后,传入神经支配部分得以保留,肘关节屈曲挛缩明显较轻。节后损伤后肌梭退化,但节前损伤后肌梭得以保留。节后损伤后去神经支配的肌梭中ErbB信号通路失活,但节前损伤后保留传入神经支配的肌梭中ErbB信号通路活性得以保留。节前和节后损伤均与梭外肌纤维中ErbB信号通路的上调有关。

结论

NBPI后的挛缩与肌梭退化和肌梭ErbB信号通路活性丧失有关。保留传入神经支配可维持肌梭发育和ErbB信号通路活性,并预防挛缩。

临床意义

作为充血性心力衰竭治疗方法正在研究的ErbB信号通路的药物调节,可能能够重现传入神经支配在肌梭发育和挛缩预防中的保护作用。肌梭的保留也可能对本体感觉和运动学习有影响,这两者在NBPI中均受损。

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