High-fat diet-induced obesity exacerbated collagenase-induced tendon injury with upregulation of interleukin-1beta and matrix metalloproteinase-1.

IF 2.8 4区 医学 Q3 CELL BIOLOGY Connective Tissue Research Pub Date : 2024-10-04 DOI:10.1080/03008207.2024.2409751
Samuel Ka-Kin Ling, Zuru Liang, Pauline Po Yee Lui
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Abstract

Aims: Obesity increases tendinopathy's risk, but its mechanisms remain unclear. This study examined the effect of high-fat diet (HFD)-induced obesity on the outcomes and inflammation of collagenase-induced (CI) tendon injury.

Methods: Mice were fed with standard chow (SC) or HFD for 12 weeks. Bacterial collagenase I or saline was injected over the patellar tendons of each mouse. At weeks 2 and 8 post-injection, the patellar tendons were harvested for histology, immunohistochemical staining, and gait analysis. The difference (Δ) of limb-idleness index (LII) at the time of post-injury and pre-injury states was calculated. Biomechanical test of tendons was also performed at week 8 post-injection.

Results: HFD aggravated CI tendon injury with an increase in vascularity and cellularity compared to SC treatment. The histopathological score (week 2: p = 0.025; week 8: p = 0.013) and ΔLII (week 2: p = 0.012; week 8: p = 0.005) were significantly higher in the HFD group compared to those in the SC group after CI tendon injury. Stiffness (saline: p = 0.003; CI: p = 0.010), ultimate stress (saline: p < 0.001; CI: p = 0.006), and Young's modulus (saline: p = 0.017; CI: p = 0.007) were significantly lower in the HFD group compared to the SC group at week 8 after saline or collagenase injection. HFD induced higher expression of IL-1β (week 2: p = 0.010; week 8: p = 0.025) and MMP-1 (week 2: p = 0.010; week 8: p = 0.004) compared to SC treatment after CI tendon injury at both time points.

Conclusions: HFD-induced obesity exacerbated histopathological, functional, and biomechanical changes in the CI tendon injury model, which was associated with an upregulation of IL-1β and MMP-1.

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高脂饮食诱发的肥胖会加剧胶原酶诱发的肌腱损伤,并上调白细胞介素-1β和基质金属蛋白酶-1。
目的:肥胖会增加肌腱病的风险,但其机制仍不清楚。本研究探讨了高脂饮食(HFD)诱导的肥胖对胶原酶诱导(CI)肌腱损伤的结果和炎症的影响:方法:用标准饲料(SC)或高脂饮食喂养小鼠12周。在每只小鼠的髌腱上注射细菌胶原酶 I 或生理盐水。注射后第2周和第8周,取髌腱进行组织学、免疫组化染色和步态分析。计算受伤后与受伤前的肢体瘫痪指数(LII)差值(Δ)。在注射后第8周还对肌腱进行了生物力学测试:结果:与SC治疗相比,HFD加重了CI肌腱损伤,增加了血管和细胞。CI肌腱损伤后,HFD组的组织病理学评分(第2周:p = 0.025;第8周:p = 0.013)和ΔLII(第2周:p = 0.012;第8周:p = 0.005)显著高于SC组。在注射生理盐水或胶原酶后第 8 周,HFD 组的硬度(生理盐水:p = 0.003;CI:p = 0.010)、极限应力(生理盐水:p = 0.006)和杨氏模量(生理盐水:p = 0.017;CI:p = 0.007)明显低于 SC 组。HFD诱导的IL-1β(第2周:p = 0.010;第8周:p = 0.025)和MMP-1(第2周:p = 0.010;第8周:p = 0.004)在CI肌腱损伤后的两个时间点的表达均高于SC组:结论:高脂饮食诱导的肥胖会加剧CI肌腱损伤模型的组织病理学、功能和生物力学变化,这与IL-1β和MMP-1的上调有关。
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来源期刊
Connective Tissue Research
Connective Tissue Research 生物-细胞生物学
CiteScore
6.60
自引率
3.40%
发文量
37
审稿时长
2 months
期刊介绍: The aim of Connective Tissue Research is to present original and significant research in all basic areas of connective tissue and matrix biology. The journal also provides topical reviews and, on occasion, the proceedings of conferences in areas of special interest at which original work is presented. The journal supports an interdisciplinary approach; we present a variety of perspectives from different disciplines, including Biochemistry Cell and Molecular Biology Immunology Structural Biology Biophysics Biomechanics Regenerative Medicine The interests of the Editorial Board are to understand, mechanistically, the structure-function relationships in connective tissue extracellular matrix, and its associated cells, through interpretation of sophisticated experimentation using state-of-the-art technologies that include molecular genetics, imaging, immunology, biomechanics and tissue engineering.
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