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早期跑步机跑步通过神经肽Y介导的Wnt/β-连环蛋白信号失活延迟肩袖愈合。

Early treadmill running delays rotator cuff healing via Neuropeptide Y mediated inactivation of the Wnt/β-catenin signaling.

作者信息

Chen Yang, Zhang Tao, Wan Liyang, Wang Zhanwen, Li Shengcan, Hu Jianzhong, Xu Daqi, Lu Hongbin

机构信息

Department of Sports Medicine, Xiangya Hospital, Central South University, Changsha, 410008, China.

Key Laboratory of Organ Injury, Aging and Regenerative Medicine of Hunan Province, Changsha, 410008, China.

出版信息

J Orthop Translat. 2021 Oct 11;30:103-111. doi: 10.1016/j.jot.2021.08.004. eCollection 2021 Sep.

DOI:10.1016/j.jot.2021.08.004
PMID:34722153
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8517718/
Abstract

BACKGROUND

Defining the optimal rehabilitation programs for rotator cuff healing remains a challenge. Early treadmill running may have negative effects on tendon-bone interface (TBI) healing with increased expression of Neuropeptide Y (NPY). However, the underlying mechanism is still unknown.

METHODS

The mice were randomly assigned to four groups: control group, treadmill group, treadmill ​+ ​BIBO3304 group and BIBO3304 group alone. Specifically, the control group was allowed free cage activity without any treatment after surgery. The treadmill group received early treadmill running initiated from postoperative day 2. The treadmill ​+ ​BIBO3304 group received treadmill running combined with intra-articular injection of BIBO3304 postoperatively. The BIBO3304 group only received type 1 NPY receptor (Y1 receptor, Y1R) antagonist BIBO3304 postoperatively. Healing outcomes of the rotator cuff were evaluated by histological analysis, synchrotron radiation micro-computed tomography (SR-μCT) scanning, and biomechanical testing at 4 and 8 weeks after surgery. The expression of NPY and its Y1 receptor during the treadmill running were tested by immunofluorescence. In addition, the related signaling pathway of Neuropeptide Y among all groups was detected by immunohistochemistry and western-blot.

RESULTS

Immunofluorescence results show that early treadmill training could lead to a significant increase in the expression of NPY at the healing site, and Y1R was widely expressed in both normal or injured rotator cuff without statistical difference. At the same time, early treadmill running delayed the healing of rotator cuff, as indicated with unsatisfactory outcomes, including a significantly lower histological score, decreased bone formation and inferior biomechanical properties at postoperative week 4 and 8. Moreover, the use of BIBO3304 could partly alleviate the negative effects of early treadmill running on the healing of rotator cuff and promote the natural healing process of rotator cuff, as evidenced by significant differences observed between the treadmill and treadmill ​+ ​BIBO3304 groups, as well as observed between the control and BIBO3304 groups. On the other hand, the expressions of Wnt3a and β-catenin in the treadmill group were significantly lower compared with the other groups, while the expression in the BIBO3304 group was the highest, as evaluated by immunohistochemistry and western-blot.

CONCLUSIONS

Early treadmill running increased the expression of NPY at the RC healing site, which might burden the expression of Wnt3a/β-catenin and delay the healing process, inhibition of Y1 receptor with BIBO3304 could promote bone-tendon healing through the Wnt/β-catenin signaling.The translational potential of this article: This is the first study to evaluate the specific role of the NPY-Y1R axis and its underlying mechanism by which early treadmill running delays bone-tendon healing. Further, our study may provide references of precise and individualized exercise-based rehabilitation strategies for TBI healing in clinic.

THE TRANSLATIONAL POTENTIAL OF THIS ARTICLE

This is the first study to evaluate the specific role of the NPY-Y1R axis and its underlying mechanism by which early treadmill running delays bone-tendon healing. Further, our study may provide references of precise and individualized exercise-based rehabilitation strategies for TBI healing in clinic.

摘要

背景

确定肩袖愈合的最佳康复方案仍然是一项挑战。早期跑步机跑步可能会对肌腱-骨界面(TBI)愈合产生负面影响,导致神经肽Y(NPY)表达增加。然而,其潜在机制仍不清楚。

方法

将小鼠随机分为四组:对照组、跑步机组、跑步机+BIBO3304组和单独的BIBO3304组。具体而言,对照组在手术后允许自由在笼内活动,不接受任何治疗。跑步机组从术后第2天开始进行早期跑步机跑步。跑步机+BIBO3304组在术后接受跑步机跑步并联合关节内注射BIBO3304。BIBO3304组仅在术后接受1型NPY受体(Y1受体,Y1R)拮抗剂BIBO3304。在术后4周和8周,通过组织学分析、同步辐射微计算机断层扫描(SR-μCT)和生物力学测试评估肩袖的愈合结果。通过免疫荧光检测跑步机跑步过程中NPY及其Y1受体的表达。此外,通过免疫组织化学和蛋白质免疫印迹法检测所有组中神经肽Y的相关信号通路。

结果

免疫荧光结果显示,早期跑步机训练可导致愈合部位NPY表达显著增加,且Y1R在正常或受伤的肩袖中均广泛表达,无统计学差异。同时,早期跑步机跑步延迟了肩袖的愈合,结果不理想,包括术后第4周和第8周组织学评分显著降低、骨形成减少和生物力学性能较差。此外,使用BIBO3304可部分减轻早期跑步机跑步对肩袖愈合的负面影响,并促进肩袖的自然愈合过程,跑步机组与跑步机+BIBO3304组之间以及对照组与BIBO3304组之间观察到的显著差异证明了这一点。另一方面,通过免疫组织化学和蛋白质免疫印迹法评估,跑步机组中Wnt3a和β-连环蛋白的表达明显低于其他组,而BIBO3304组中的表达最高。

结论

早期跑步机跑步增加了肩袖愈合部位NPY的表达,这可能会加重Wnt3a/β-连环蛋白的表达并延迟愈合过程,用BIBO3304抑制Y1受体可通过Wnt/β-连环蛋白信号促进骨-肌腱愈合。

本文的转化潜力

这是第一项评估NPY-Y1R轴的具体作用及其潜在机制的研究,早期跑步机跑步通过该机制延迟骨-肌腱愈合。此外,我们的研究可能为临床上TBI愈合的精确和个性化运动康复策略提供参考。

本文的转化潜力

这是第一项评估NPY-Y1R轴的具体作用及其潜在机制的研究,早期跑步机跑步通过该机制延迟骨-肌腱愈合。此外,我们的研究可能为临床上TBI愈合的精确和个性化运动康复策略提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcae/8517718/c56aa14e80e6/gr9.jpg
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