代谢系统分析确定了一种涉及血栓素A2和LTC4的创伤内皮病(EoT)患者休克的新机制

Q1 Medicine Matrix Biology Plus Pub Date : 2022-08-01 DOI:10.1016/j.mbplus.2022.100115
Hanne H. Henriksen , Igor Marín de Mas , Helena Herand , Joseph Krocker , Charles E. Wade , Pär I. Johansson
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引用次数: 4

摘要

目的创伤性内皮病变(EoT),根据循环中syndecan-1水平≥40 ng/mL的定义,已报道与输血需求显著增加和30天死亡率翻倍相关。糖萼脱落增加表明内皮细胞膜组成对临床结果很重要,这是本研究的基本原理。结果采用质谱法对95例重型外伤患者的血浆代谢组进行了检测,并采用偏最小二乘判别法对急性外伤患者与非急性外伤患者进行了比较。确定琥珀酸是区分EoT和非EoT患者的首要代谢物(VIP评分= 3)。通过将相应的血浆代谢组数据整合到基因组尺度的代谢网络重建分析中,推断EoT和非EoT患者的代谢通量谱,并对各组代谢能力进行功能研究。模型预测显示,与非EoT患者相比,EoT患者的胆固醇代谢降低,继发于甲羟戊酸合成受损。细胞内任务分析表明,与非EoT患者相比,EoT患者的血栓素a2和白三烯合成减少,肉毒碱棕榈酰基转移酶I活性降低。敏感性分析还显示,EoT患者的α -亚麻酸对类二十烷酸相关代谢任务的依赖性非常高。模型驱动的内皮细胞代谢分析发现,与非EoT患者相比,EoT患者的潜在新靶点是血栓素A2和白三烯合成受损。微血管中血栓素A2和白三烯可用性的降低会损害血管收缩能力,从而可能导致EoT患者休克。这些发现得到了大量科学文献的支持;但是,需要对这些发现进行进一步调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Metabolic systems analysis identifies a novel mechanism contributing to shock in patients with endotheliopathy of trauma (EoT) involving thromboxane A2 and LTC4

Purpose

Endotheliopathy of trauma (EoT), as defined by circulating levels of syndecan-1 ≥ 40 ng/mL, has been reported to be associated with significantly increased transfusion requirements and a doubled 30-day mortality. Increased shedding of the glycocalyx points toward the endothelial cell membrane composition as important for the clinical outcome being the rationale for this study.

Results

The plasma metabolome of 95 severely injured trauma patients was investigated by mass spectrometry, and patients with EoT vs. non-EoT were compared by partial least square-discriminant analysis, identifying succinic acid as the top metabolite to differentiate EoT and non-EoT patients (VIP score = 3). EoT and non-EoT patients’ metabolic flux profile was inferred by integrating the corresponding plasma metabolome data into a genome-scale metabolic network reconstruction analysis and performing a functional study of the metabolic capabilities of each group. Model predictions showed a decrease in cholesterol metabolism secondary to impaired mevalonate synthesis in EoT compared to non-EoT patients. Intracellular task analysis indicated decreased synthesis of thromboxanA2 and leukotrienes, as well as a lower carnitine palmitoyltransferase I activity in EoT compared to non-EoT patients. Sensitivity analysis also showed a significantly high dependence of eicosanoid-associated metabolic tasks on alpha-linolenic acid as unique to EoT patients.

Conclusions

Model-driven analysis of the endothelial cells’ metabolism identified potential novel targets as impaired thromboxane A2 and leukotriene synthesis in EoT patients when compared to non-EoT patients. Reduced thromboxane A2 and leukotriene availability in the microvasculature impairs vasoconstriction ability and may thus contribute to shock in EoT patients. These findings are supported by extensive scientific literature; however, further investigations are required on these findings.

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来源期刊
Matrix Biology Plus
Matrix Biology Plus Medicine-Histology
CiteScore
9.00
自引率
0.00%
发文量
25
审稿时长
105 days
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