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酰基氨基葡萄糖修饰组学揭示 ACLY 是幼鼠脓毒症的潜在靶点

An -GlcNAcylomic Approach Reveals ACLY as a Potential Target in Sepsis in the Young Rat.

机构信息

Université de Nantes, CHU Nantes, CNRS, INSERM, l'Institut du Thorax, F-44000 Nantes, France.

Pediatric Intensive Care Unit, CHU de Nantes, F-44000 Nantes, France.

出版信息

Int J Mol Sci. 2021 Aug 26;22(17):9236. doi: 10.3390/ijms22179236.

Abstract

Sepsis in the young population, which is particularly at risk, is rarely studied. -GlcNAcylation is a post-translational modification involved in cell survival, stress response and metabolic regulation. -GlcNAc stimulation is beneficial in adult septic rats. This modification is physiologically higher in the young rat, potentially limiting the therapeutic potential of -GlcNAc stimulation in young septic rats. The aim is to evaluate whether -GlcNAc stimulation can improve sepsis outcome in young rats. Endotoxemic challenge was induced in 28-day-old rats by lipopolysaccharide injection ( O111:B4, 20 mg·kg) and compared to control rats (NaCl 0.9%). One hour after lipopolysaccharide injection, rats were randomly assigned to no therapy, fluidotherapy (NaCl 0.9%, 10 mL·kg) ± NButGT (10 mg·kg) to increase -GlcNAcylation levels. Physiological parameters and plasmatic markers were evaluated 2h later. Finally, untargeted mass spectrometry was performed to map cardiac -GlcNAcylated proteins. Lipopolysaccharide injection induced shock with a decrease in mean arterial pressure and alteration of biological parameters ( < 0.05). NButGT, contrary to fluidotherapy, was associated with an improvement of arterial pressure ( < 0.05). ATP citrate lyase was identified among the -GlcNAcylated proteins. In conclusion, -GlcNAc stimulation improves outcomes in young septic rats. Interestingly, identified -GlcNAcylated proteins are mainly involved in cellular metabolism.

摘要

在易患败血症的年轻人群中,此类疾病研究甚少。-GlcNAc 酰化是一种参与细胞存活、应激反应和代谢调节的翻译后修饰。-GlcNAc 刺激对成年败血症大鼠有益。年轻大鼠的这种修饰生理性更高,可能限制了年轻败血症大鼠中 -GlcNAc 刺激的治疗潜力。目的是评估 -GlcNAc 刺激是否能改善年轻大鼠败血症的结局。通过注射脂多糖(O111:B4,20mg·kg)诱导 28 日龄大鼠发生内毒素血症挑战,并与对照大鼠(0.9%NaCl)进行比较。脂多糖注射 1 小时后,大鼠随机分为无治疗组、液体治疗组(0.9%NaCl,10mL·kg)±NButGT(10mg·kg)以增加 -GlcNAc 水平。2 小时后评估生理参数和血浆标志物。最后,进行非靶向质谱分析以绘制心脏 -GlcNAc 化蛋白图谱。脂多糖注射引起休克,表现为平均动脉压下降和生物学参数改变(<0.05)。与液体治疗相反,NButGT 与动脉压的改善相关(<0.05)。鉴定到的 -GlcNAc 化蛋白中包括柠檬酸裂解酶。结论:-GlcNAc 刺激可改善年轻败血症大鼠的结局。有趣的是,鉴定到的 -GlcNAc 化蛋白主要参与细胞代谢。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b65a/8430499/b73f3d3c0680/ijms-22-09236-g001.jpg

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