Gihring Adrian, Gärtner Fabian, Liu Congxing, Hoenicka Markus, Wabitsch Martin, Knippschild Uwe, Xu Pengfei
Department of General and Visceral Surgery, Surgery Center, Ulm University Medical Center, Ulm, Germany.
Department of Cardio-Thoracic and Vascular Surgery, Ulm University Medical Center, Ulm, Germany.
Front Physiol. 2020 Jul 28;11:849. doi: 10.3389/fphys.2020.00849. eCollection 2020.
Obesity has been described as a major factor of health risk in modern society. Next to intricately linked comorbidities like coronary artery disease or diabetes, an influence of obesity on regeneration after muscle injury has been described previously. However, the influence of obesity on tissue regeneration in a combined trauma, merging the more systemic influence of a blunt lung trauma and the local blunt muscle trauma, has not been investigated yet. Therefore, the aim of this study was to investigate the influence of obesity on regeneration in a mouse model that combined both muscle and thorax trauma. Using gene expression analysis, a focus was put on the structure as well as the organization of the extracellular matrix and on functional satellite cell physiology. An increased amount of debris in the lung of obese mice compared to normal weight mice up to 192 h after combined trauma based on visual assessment can be reported which is accompanied by a decreased response of in obese mice. Additionally, a delayed and elongated response of inhibitor genes like has been revealed in obese mice. This elongated response to the trauma in obese mice can also be seen in plasma based on increased levels of pro-inflammatory chemo- and cytokines (IL-6, MCP-1, and IL 23) 192 h post trauma. In addition to changes in the lung, morphological analysis of the injured of the left hind leg in lean and diet-induced obese mice revealed deposition of fat in the regenerating muscle in obese animals hindering the structure of a compact muscle. Additionally, decreased activation of satellite cells and changes in organization and build-up of the ECM could be detected, finally leading to a decreased stability of the regenerated muscle in obese mice. Both factors contribute to an attenuated response to the trauma by obese mice which is reflected by a statistically significant decrease in muscle force of obese mice compared to lean mice 192 h post trauma induction.
肥胖被认为是现代社会健康风险的主要因素。除了与冠状动脉疾病或糖尿病等复杂相关的合并症外,肥胖对肌肉损伤后再生的影响此前已有描述。然而,肥胖对复合创伤中组织再生的影响尚未得到研究,复合创伤合并了钝性肺创伤的更全身性影响和局部钝性肌肉创伤。因此,本研究的目的是在一个同时合并肌肉和胸部创伤的小鼠模型中研究肥胖对再生的影响。通过基因表达分析,重点关注细胞外基质的结构和组织以及功能性卫星细胞生理学。基于视觉评估,可报告在复合创伤后192小时内,肥胖小鼠肺部的碎片量比正常体重小鼠增加,同时肥胖小鼠的反应降低。此外,在肥胖小鼠中发现了如等抑制基因的延迟和延长反应。基于创伤后192小时促炎趋化因子和细胞因子(IL-6、MCP-1和IL 23)水平的升高,在血浆中也可观察到肥胖小鼠对创伤反应的延长。除了肺部的变化外,对瘦小鼠和饮食诱导肥胖小鼠左后腿受伤肌肉的形态学分析显示,肥胖动物再生肌肉中有脂肪沉积,阻碍了致密肌肉的结构。此外,还可检测到卫星细胞的激活减少以及细胞外基质的组织和积累变化,最终导致肥胖小鼠再生肌肉的稳定性降低。这两个因素导致肥胖小鼠对创伤的反应减弱,这表现为在创伤诱导后192小时,肥胖小鼠与瘦小鼠相比肌肉力量有统计学意义的下降。