脊髓组织的区域生物力学特征:动态机械响应。

IF 4.3 3区 工程技术 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Frontiers in Bioengineering and Biotechnology Pub Date : 2024-08-16 eCollection Date: 2024-01-01 DOI:10.3389/fbioe.2024.1439323
Chen Jin, Jiang-Ming Yu, Ran Li, Xiao-Jian Ye
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引用次数: 0

摘要

表征脊髓组织的动态机械特性对于全面了解脊髓损伤的机制非常重要。然而,由于脊髓具有异质性,对其复杂粘弹特性的研究远远不够。为了研究脊髓生物力学特性的区域性差异,我们提供了一种力学表征方法(即动态力学分析),该方法有助于在小变形的动态条件下对脊髓进行稳健的体外测量。在死后 2 小时内,以 0.05、0.10、0.50 和 1.00 Hz 的正弦频率对组织表面进行加载-卸载循环。我们报告了脊髓组织的主要响应特征(如非线性、速率依赖性、滞后和调节)取决于解剖学起源,并通过测量峰值力、模量、滞后和能量损失来量化粘弹性特性。在所有三个解剖区域(颈椎、胸椎和腰椎脊髓组织),复合模量、存储模量和损失模量对应变率增加的反应相似。值得注意的是,活体脊髓组织的复合模量值随着测试频率的增加而非线性上升。此外,在每个应变率下,胸段脊髓组织的刚度都明显高于颈段或腰段脊髓组织,复合模量值大约是腰段组织的 1.5 倍。在应变率介于 0.05 和 0.50 Hz 之间时,胸段脊髓(即分别为 0.26、0.25、0.06)和腰段脊髓(即分别为 0.27、0.25、0.07)的 tan δ 值相似,分别高于颈段脊髓(即分别为 0.21、0.21、0.04)。在变形率相对较高的情况下,调节效应往往更大。有趣的是,无论加载速率如何,在所有三个解剖区域中均未观察到明显的调节比差异。这些发现为进一步比较健康脊髓和病变脊髓奠定了基础,有助于未来脊髓支架的开发,也有助于增进我们对神经科学的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regional biomechanical characterization of the spinal cord tissue: dynamic mechanical response.

Characterizing the dynamic mechanical properties of spinal cord tissue is deemed important for developing a comprehensive knowledge of the mechanisms underlying spinal cord injury. However, complex viscoelastic properties are vastly underexplored due to the spinal cord shows heterogeneous properties. To investigate regional differences in the biomechanical properties of spinal cord, we provide a mechanical characterization method (i.e., dynamic mechanical analysis) that facilitates robust measurement of spinal cord ex vivo, at small deformations, in the dynamic regimes. Load-unload cycles were applied to the tissue surface at sinusoidal frequencies of 0.05, 0.10, 0.50 and 1.00 Hz ex vivo within 2 h post mortem. We report the main response features (e.g., nonlinearities, rate dependencies, hysteresis and conditioning) of spinal cord tissue dependent on anatomical origin, and quantify the viscoelastic properties through the measurement of peak force, moduli, and hysteresis and energy loss. For all three anatomical areas (cervical, thoracic, and lumbar spinal cord tissues), the compound, storage, and loss moduli responded similarly to increasing strain rates. Notably, the complex modulus values of ex vivo spinal cord tissue rose nonlinearly with rising test frequency. Additionally, at every strain rate, it was shown that the tissue in the thoracic spinal cord was significantly more rigid than the tissue in the cervical or lumbar spinal cord, with compound modulus values roughly 1.5-times that of the lumbar region. At strain rates between 0.05 and 0.50 Hz, tan δ values for thoracic (that is, 0.26, 0.25, 0.06, respectively) and lumbar (that is, 0.27, 0.25, 0.07, respectively) spinal cord regions were similar, respectively, which were higher than cervical (that is, 0.21, 0.21, 0.04, respectively) region. The conditioning effects tend to be greater at relative higher deformation rates. Interestingly, no marked difference of conditioning ratios is observed among all three anatomical regions, regardless of loading rate. These findings lay a foundation for further comparison between healthy and diseased spinal cord to the future development of spinal cord scaffold and helps to advance our knowledge of neuroscience.

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来源期刊
Frontiers in Bioengineering and Biotechnology
Frontiers in Bioengineering and Biotechnology Chemical Engineering-Bioengineering
CiteScore
8.30
自引率
5.30%
发文量
2270
审稿时长
12 weeks
期刊介绍: The translation of new discoveries in medicine to clinical routine has never been easy. During the second half of the last century, thanks to the progress in chemistry, biochemistry and pharmacology, we have seen the development and the application of a large number of drugs and devices aimed at the treatment of symptoms, blocking unwanted pathways and, in the case of infectious diseases, fighting the micro-organisms responsible. However, we are facing, today, a dramatic change in the therapeutic approach to pathologies and diseases. Indeed, the challenge of the present and the next decade is to fully restore the physiological status of the diseased organism and to completely regenerate tissue and organs when they are so seriously affected that treatments cannot be limited to the repression of symptoms or to the repair of damage. This is being made possible thanks to the major developments made in basic cell and molecular biology, including stem cell science, growth factor delivery, gene isolation and transfection, the advances in bioengineering and nanotechnology, including development of new biomaterials, biofabrication technologies and use of bioreactors, and the big improvements in diagnostic tools and imaging of cells, tissues and organs. In today`s world, an enhancement of communication between multidisciplinary experts, together with the promotion of joint projects and close collaborations among scientists, engineers, industry people, regulatory agencies and physicians are absolute requirements for the success of any attempt to develop and clinically apply a new biological therapy or an innovative device involving the collective use of biomaterials, cells and/or bioactive molecules. “Frontiers in Bioengineering and Biotechnology” aspires to be a forum for all people involved in the process by bridging the gap too often existing between a discovery in the basic sciences and its clinical application.
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