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将临床常用药物与脊髓损伤啮齿动物的后肢伸展相结合。

Combining clinically common drugs with hindlimb stretching in spinal cord injured rodents.

机构信息

Interdisciplinary Program in Translational Neuroscience, University of Louisville, Louisville, KY, USA.

Department of Anatomical Sciences and Neurobiology, School of Medicine, University of Louisville, Louisville, KY, USA.

出版信息

Spinal Cord. 2024 Oct;62(10):574-583. doi: 10.1038/s41393-024-01023-3. Epub 2024 Aug 26.

Abstract

STUDY DESIGN

Preclinical pilot study.

OBJECTIVES

To explore peripheral and central nociceptive mechanisms that contribute to muscle stretch-induced locomotor deficits following spinal cord injury.

SETTING

Kentucky Spinal Cord Injury Research Center, Louisville, KY, USA.

METHODS

Ten female Sprague-Dawley rats received moderate, 25 g/cm T10 contusion injuries and recovered for 4 weeks. Rats were divided into three groups: Morphine/Ibuprofen-treated, Acetaminophen/Baclofen-treated, and saline control. Each group received daily hindlimb muscle stretching during weeks 4, 5, 9, and 10 post-injury and drugs were administered with stretching during weeks 4 and 9 only. Locomotor function was assessed throughout the experiment using the BBB Open Field Locomotor Scale. Hindlimb responses including spasticity, writhing, and clonic-like vibrations during muscle stretching were classified and scored.

RESULTS

Consistent with our previous studies, hindlimb muscle stretching caused significant deficits in locomotor recovery following spinal cord injury. Baclofen and Ibuprofen partially mitigated the stretching effect, but none of the drugs significantly prevented the drop in locomotor function during stretching. Interestingly, treatment with Baclofen or Ibuprofen significantly reduced hindlimb responses such as spasticity and writhing during stretching, while Morphine exacerbated clonic-like vibrations in response to stretching maneuvers.

CONCLUSIONS

These findings suggest that stretching may inhibit locomotor recovery through combined mechanisms of peripheral inflammation and sensitization of nociceptive afferents. When combined with central sprouting and loss of descending controls after SCI, this results in exaggerated nociceptive input during stretching. The inability of the applied clinical drugs to mitigate the detrimental effects of stretching highlights the complexity of the stretching phenomenon and emphasizes the need for further investigation.

摘要

研究设计

临床前试点研究。

目的

探索导致脊髓损伤后肌肉拉伸引起运动功能障碍的周围和中枢伤害感受机制。

地点

美国肯塔基州脊髓损伤研究中心,路易斯维尔。

方法

10 只雌性 Sprague-Dawley 大鼠接受中度(25g/cm)T10 挤压伤,恢复 4 周。大鼠分为三组:吗啡/布洛芬治疗组、对乙酰氨基酚/巴氯芬治疗组和生理盐水对照组。每组在损伤后第 4、5、9 和 10 周接受每日后肢肌肉拉伸,仅在第 4 和 9 周拉伸时给予药物。整个实验过程中使用 BBB 旷场运动量表评估运动功能。在肌肉拉伸过程中对后肢反应(包括痉挛、扭动和阵挛样振动)进行分类和评分。

结果

与我们之前的研究一致,后肢肌肉拉伸导致脊髓损伤后运动功能恢复明显受损。巴氯芬和布洛芬部分减轻了拉伸的影响,但没有一种药物能显著防止在拉伸过程中运动功能下降。有趣的是,巴氯芬或布洛芬治疗显著减少了拉伸过程中的后肢反应,如痉挛和扭动,而吗啡加剧了对拉伸动作的阵挛样振动。

结论

这些发现表明,拉伸可能通过外周炎症和伤害感受传入敏化的综合机制抑制运动恢复。当与 SCI 后中枢发芽和下行控制丧失结合时,这会导致拉伸时伤害性传入增加。应用的临床药物无法减轻拉伸的有害影响,突出了拉伸现象的复杂性,并强调了进一步研究的必要性。

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