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椎间盘退变和下腰痛取决于轴向压缩的持续时间和幅度。

Intervertebral Disc Degeneration and Low Back Pain Depends on Duration and Magnitude of Axial Compression.

机构信息

Henan Luoyang Orthopedic Hospital (Henan Provincial Orthopedic Hospital), Henan Provincial Orthopedic Institute, Zhengzhou 450000, China.

Henan University of Chinese Medicine, Zhengzhou 450046, China.

出版信息

Oxid Med Cell Longev. 2022 Apr 29;2022:1045999. doi: 10.1155/2022/1045999. eCollection 2022.

Abstract

PURPOSE

The pathological role of axial stress in intervertebral disc degeneration (IDD) is controversial, and there was no quantified study until now. Here, we tried to clarify the correlation between IDD or low back pain (LBP) and axial stress at different duration and magnitude in vitro and in vivo.

METHOD

In vitro, the gene expression of aggrecan, matrix metalloproteinase-3 (MMP3), calcitonin gene-related peptide (CGRP), and substance P (SP) was measured when nucleus pulposus cells (NPCs) were compressed under gradual severity. In vivo, a measurable Ilizarov-type compression apparatus was established for single coccygeal (Co) intervertebral disc (IVD) compression of Co7-8 in mouse. Gradient stress was placed at 0.4 Mpa (mild), 0.8 Mpa (moderate), and 1.2 Mpa (severe) for three days to investigate the effect of the magnitude of axial stress. Additionally, mild compression with 3, 7, and 14 days was used to determine the effect of the duration of axial stress. Subsequently, we evaluated the severity of IDD and LBP by radiological X-ray film; histological examination with H&E staining; immunohistochemical analysis with collagen II, aggrecan, and CGRP staining; and western blot analysis with collagen II, aggrecan, MMP-3, and interleukin-1 (IL-1).

RESULTS

When NPCs suffered gradual increased mechanical stress, the cells exhibited gradual downregulated expression of extracellular matrix (ECM)-related gene of aggrecan, upregulated expression of IDD-related gene of MMP3, and LBP-related gene of CGRP and SP. In the meantime, with different magnitudes of axial stress, the IVD showed progressively severe IDD and LBP, with gradual narrowing intervertebral height, destruction of IVD anatomy, decreased ECM, and increased catabolic factors and proalgesic peptides.

CONCLUSION

Axial compression is one of the critical pathological factors to cause IDD and LBP, and there was a strong positive correlation depended on the duration and magnitude of compression.

摘要

目的

轴向应力在椎间盘退变(IDD)中的病理作用存在争议,目前尚无定量研究。本研究试图在体外和体内阐明不同持续时间和程度的 IDD 或下腰痛(LBP)与轴向应力之间的相关性。

方法

在体外,当髓核细胞(NPC)逐渐受到严重程度的压缩时,测量软骨寡聚基质蛋白(aggrecan)、基质金属蛋白酶 3(MMP3)、降钙素基因相关肽(CGRP)和 P 物质(SP)的基因表达。在体内,建立了可测量的伊里扎洛夫型压缩装置,用于对小鼠 Co7-8 单一尾骨(Co)椎间盘(IVD)进行压缩。梯度应力分别施加在 0.4 MPa(轻度)、0.8 MPa(中度)和 1.2 MPa(重度)3 天,以研究轴向应力大小的影响。此外,使用 3、7 和 14 天的轻度压缩来确定轴向应力持续时间的影响。随后,我们通过放射 X 射线片评估 IDD 和 LBP 的严重程度;通过 H&E 染色进行组织学检查;通过胶原蛋白 II、aggrecan 和 CGRP 染色进行免疫组织化学分析;通过胶原蛋白 II、aggrecan、MMP-3 和白细胞介素 1(IL-1)的 Western blot 分析。

结果

当 NPC 受到逐渐增加的机械应力时,细胞表现出细胞外基质(ECM)相关基因 aggrecan 的逐渐下调表达,IDD 相关基因 MMP3 和 LBP 相关基因 CGRP 和 SP 的上调表达。同时,随着轴向应力的不同程度,IVD 表现出逐渐严重的 IDD 和 LBP,椎间高度逐渐变窄,IVD 解剖结构破坏,ECM 减少,分解代谢因子和致痛肽增加。

结论

轴向压缩是导致 IDD 和 LBP 的关键病理因素之一,与压缩的持续时间和程度呈强正相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e96/9076309/2454aaa5cf27/OMCL2022-1045999.001.jpg

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