Antenatal creatine supplementation reduces persistent fetal lung inflammation and oxidative stress in an ovine model of chorioamnionitis.

IF 3.6 2区 医学 Q1 PHYSIOLOGY American journal of physiology. Lung cellular and molecular physiology Pub Date : 2024-07-01 Epub Date: 2024-05-07 DOI:10.1152/ajplung.00241.2023
Y Jane Choi, Ellen Williams, Mar Janna Dahl, Sebastian E Amos, Christopher James, Angelo P Bautista, Veena Kurup, Gabrielle C Musk, Helen Kershaw, Peter G Arthur, Anthony Kicic, Yu Suk Choi, Jessica R Terrill, J Jane Pillow
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Abstract

Chorioamnionitis is a common antecedent of preterm birth and induces inflammation and oxidative stress in the fetal lungs. Reducing inflammation and oxidative stress in the fetal lungs may improve respiratory outcomes in preterm infants. Creatine is an organic acid with known anti-inflammatory and antioxidant properties. The objective of the study was to evaluate the efficacy of direct fetal creatine supplementation to reduce inflammation and oxidative stress in fetal lungs arising from an in utero proinflammatory stimulus. Fetal lambs (n = 51) were instrumented at 90 days gestation to receive a continuous infusion of creatine monohydrate (6 mg·kg-1·h-1) or saline for 17 days. Maternal chorioamnionitis was induced with intra-amniotic lipopolysaccharide (LPS; 1 mg, O55:H6) or saline 7 days before delivery at 110 days gestation. Tissue creatine content was assessed with capillary electrophoresis, and inflammatory markers were analyzed with Luminex Magpix and immunohistochemistry. Oxidative stress was measured as the level of protein thiol oxidation. The effects of LPS and creatine were analyzed using a two-way ANOVA. Fetal creatine supplementation increased lung creatine content by 149% (PCr < 0.0001) and had no adverse effects on lung morphology. LPS-exposed groups showed increased levels of interleukin-8 in the bronchoalveolar lavage (PLPS < 0.0001) and increased levels of CD45+ leukocytes (PLPS < 0.0001) and MPO+ (PLPS < 0.0001) cells in the lung parenchyma. Creatine supplementation significantly reduced the levels of CD45+ (PCr = 0.045) and MPO+ cells (PCr = 0.012) in the lungs and reduced thiol oxidation in plasma (PCr < 0.01) and lung tissue (PCr = 0.02). In conclusion, fetal creatine supplementation reduced markers of inflammation and oxidative stress in the fetal lungs arising from chorioamnionitis.NEW & NOTEWORTHY We evaluated the effect of antenatal creatine supplementation to reduce pulmonary inflammation and oxidative stress in the fetal lamb lungs arising from lipopolysaccharide (LPS)-induced chorioamnionitis. Fetal creatine supplementation increased lung creatine content and had no adverse effects on systemic fetal physiology and overall lung architecture. Importantly, fetuses that received creatine had significantly lower levels of inflammation and oxidative stress in the lungs, suggesting an anti-inflammatory and antioxidant benefit of creatine.

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在绒毛膜羊膜炎的绵羊模型中,产前补充肌酸可减少胎儿肺部持续炎症和氧化应激。
背景绒毛膜羊膜炎是早产的常见先兆,会诱发胎儿肺部炎症和氧化应激。减轻胎儿肺部的炎症和氧化应激可改善早产儿的呼吸系统预后。肌酸是一种有机酸,具有已知的抗炎和抗氧化特性。目的 评估直接补充胎儿肌酸对减少胎儿肺部因子宫内促炎症刺激而产生的炎症和氧化应激的疗效。方法 在妊娠 90 天时对胎儿羔羊(n=51)进行检测,连续输注一水肌酸(6 mgkg-1h-1)或生理盐水 17 天。在羔羊妊娠 110 天分娩前七天,用羊膜腔内脂多糖(LPS;1 毫克,O55:H6)或生理盐水诱发母体绒毛膜羊膜炎。组织肌酸含量通过毛细管电泳进行评估,炎症标记物通过 Luminex Magpix 和免疫组化进行分析。氧化应激以蛋白质硫醇氧化水平来衡量。采用双向方差分析法分析 LPS 和肌酸的影响。结果 补充胎儿肌酸可使肺部肌酸含量增加 149%(PCrLPS+白细胞(PLPS+(PCr=0.045)和 MPO+细胞(PCr=0.012)),并减少血浆中的硫醇氧化(PCrCr=0.02)。结论 补充胎儿肌酸可减少绒毛膜羊膜炎引起的胎儿肺部炎症和氧化应激标记物。
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来源期刊
CiteScore
9.20
自引率
4.10%
发文量
146
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Lung Cellular and Molecular Physiology publishes original research covering the broad scope of molecular, cellular, and integrative aspects of normal and abnormal function of cells and components of the respiratory system. Areas of interest include conducting airways, pulmonary circulation, lung endothelial and epithelial cells, the pleura, neuroendocrine and immunologic cells in the lung, neural cells involved in control of breathing, and cells of the diaphragm and thoracic muscles. The processes to be covered in the Journal include gas-exchange, metabolic control at the cellular level, intracellular signaling, gene expression, genomics, macromolecules and their turnover, cell-cell and cell-matrix interactions, cell motility, secretory mechanisms, membrane function, surfactant, matrix components, mucus and lining materials, lung defenses, macrophage function, transport of salt, water and protein, development and differentiation of the respiratory system, and response to the environment.
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