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首页> 外文期刊>JPEN. Journal of parenteral and enteral nutrition. >High Branched-Chain Amino Acid Concentrations Are Found in Preterm Baboons Receiving Intravenous Amino Acid Solutions and Mimic Alterations Found in Preterm Infants
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High Branched-Chain Amino Acid Concentrations Are Found in Preterm Baboons Receiving Intravenous Amino Acid Solutions and Mimic Alterations Found in Preterm Infants

机译:在预接受静脉内氨基酸溶液的早产儿狒狒中发现高分支链氨基酸浓度,并在早产儿发现的模仿改变

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摘要

Background Parenteral amino acid (AA) nutrition administration after premature birth is necessary to ensure adequate growth and neurodevelopment. However, optimizing safety and efficacy remains a major challenge. This study investigated the effects of intravenous AA administration on plasma AA profiles in premature baboons and infants. Methods Premature baboons were delivered by cesarean section at 125 days (67% gestation) and chronically ventilated. At 24 hours of life, a parenteral AA protocol comparable to the early and high AA regimens used in premature infants was initiated. Serial plasma AA concentrations were obtained on days of life (DOLs) 1, 3, and 7 and compared with concentrations at similar DOLs from preterm infants. Fetal baboon (165 +/- 2 days; 89% gestation) and term baboon plasma AA concentrations were obtained for comparison. Results Premature baboons receiving early and high parenteral AA supplementation exhibited significant differences in plasma AA concentrations compared with fetuses. In particular, concentrations of leucine, isoleucine, valine, and ornithine were elevated (fold increase: 2.14, 2.03, 1.95, and 16.5, respectively; P < 0.001) on DOL 3 vs fetuses. These alterations mimicked those found in preterm infants. Conclusion Early and high AA supplementation in extremely premature baboons significantly disrupted plasma AA concentrations. Elevated concentrations of branched-chain AAs and ornithine raise concerns for adverse neurodevelopmental outcomes. These results are consistent with those found in premature human infants and emphasize the need to optimize parenteral AA solutions for the unique metabolic requirements of premature infants. Improved technologies for rapid monitoring of AA concentrations during treatment are essential.
机译:背景技术早产后肠胃外氨基酸(AA)营养施用是为了确保充足的生长和神经发育。然而,优化安全性和疗效仍然是一个重大挑战。本研究研究了静脉内AA给药在早产儿和婴儿血浆AA谱上的影响。方法在125天(妊娠)和长期通风67%的妊娠),剖宫产段递送过早的狒狒。在24小时的生命中,启动了与早期婴儿使用的早期和高AA方案相当的肠胃外AA协议。在寿命(DOL)1,3和7天中获得串联血浆AA浓度,并与来自早产儿的类似DOL的浓度进行比较。胎儿狒狒(165 +/- 2天; 89%的妊娠)和术语狒狒血浆AA浓度进行比较。结果收到早期和高肠外AA补充的早产儿虽然与胎儿相比表现出血浆AA浓度的显着差异。特别地,亮氨酸,异氨酸,缬氨酸和鸟氨酸的浓度升高(倍数增加:2.14,2.03,1.95和16.5,P <0.001)在DOL 3 Vs胎儿上。这些改变模仿了早产儿发现的改变。结论早期和高AA补充在极早的狒狒中显着破坏了血浆AA浓度。升高的支链AAS和鸟氨酸浓度提高了神经发育结果的担忧。这些结果与早产儿发现的结果一致,并强调需要优化肠胃外AA解决方案,以获得早产儿的独特代谢要求。在治疗期间快速监测AA浓度的改进技术是必不可少的。

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