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本文引用的文献

1
Arginine de novo and nitric oxide production in disease states.疾病状态下的精氨酸从头合成和一氧化氮生成。
Am J Physiol Endocrinol Metab. 2012 Nov 15;303(10):E1177-89. doi: 10.1152/ajpendo.00284.2012. Epub 2012 Sep 25.
2
Imbalance of arginine and asymmetric dimethylarginine is associated with markers of circulatory failure, organ failure and mortality in shock patients.精氨酸和非对称性二甲基精氨酸的失衡与休克患者循环衰竭、器官衰竭和死亡率的标志物有关。
Br J Nutr. 2012 May;107(10):1458-65. doi: 10.1017/S0007114511004648. Epub 2011 Dec 1.
3
Arginase and arginine dysregulation in asthma.哮喘中的精氨酸酶与精氨酸失调
J Allergy (Cairo). 2011;2011:736319. doi: 10.1155/2011/736319. Epub 2011 Apr 26.
4
Increased protein-energy intake promotes anabolism in critically ill infants with viral bronchiolitis: a double-blind randomised controlled trial.增加蛋白质-能量摄入可促进病毒性毛细支气管炎危重症婴儿的合成代谢:一项双盲随机对照试验。
Arch Dis Child. 2011 Sep;96(9):817-22. doi: 10.1136/adc.2010.185637. Epub 2011 Jun 14.
5
Arginine and sepsis: a question of the right balance?精氨酸与脓毒症:平衡是否恰当的问题?
Crit Care Med. 2011 Jun;39(6):1569-70. doi: 10.1097/CCM.0b013e318215c1ea.
6
Acute intestinal failure in critically ill patients: is plasma citrulline the right marker?危重症患者的急性肠衰竭:瓜氨酸是否是合适的标志物?
Intensive Care Med. 2011 Jun;37(6):911-7. doi: 10.1007/s00134-011-2172-x. Epub 2011 Mar 12.
7
The ratio of arginine to dimethylarginines is reduced and predicts outcomes in patients with severe sepsis.精氨酸与二甲基精氨酸的比值降低可预测严重脓毒症患者的结局。
Crit Care Med. 2011 Jun;39(6):1351-8. doi: 10.1097/CCM.0b013e318212097c.
8
The 2009 ESPEN Sir David Cuthbertson. Citrulline: a new major signaling molecule or just another player in the pharmaconutrition game?2009 年 ESPEN 大卫·卡斯伯森爵士奖。瓜氨酸:一种新的主要信号分子,还是营养药物学游戏中的又一个参与者?
Clin Nutr. 2010 Oct;29(5):545-51. doi: 10.1016/j.clnu.2010.07.006. Epub 2010 Aug 16.
9
Exhaled nitric oxide in acute respiratory syncytial virus bronchiolitis.急性呼吸道合胞病毒细支气管炎中的呼出一氧化氮
Arch Pediatr Adolesc Med. 2010 Aug;164(8):727-31. doi: 10.1001/archpediatrics.2010.128.
10
Reduced caloric intake during endotoxemia reduces arginine availability and metabolism.脓毒症期间减少热量摄入会减少精氨酸的供应和代谢。
Am J Clin Nutr. 2010 Apr;91(4):992-1001. doi: 10.3945/ajcn.2009.27812. Epub 2010 Feb 10.

危重症婴儿的精氨酸摄入和一氧化氮合成可以通过富含蛋白质-能量的肠内配方来增加。

Arginine appearance and nitric oxide synthesis in critically ill infants can be increased with a protein-energy-enriched enteral formula.

机构信息

Department of Pediatrics, Maastricht University Medical Center, Maastricht, Netherlands.

出版信息

Am J Clin Nutr. 2013 Oct;98(4):907-16. doi: 10.3945/ajcn.112.042523. Epub 2013 Aug 14.

DOI:10.3945/ajcn.112.042523
PMID:23945723
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3778863/
Abstract

BACKGROUND

Arginine is considered an essential amino acid during critical illness in children, and supplementation of arginine has been proposed to improve arginine availability to facilitate nitric oxide (NO) synthesis. Protein-energy-enriched enteral formulas (PE-formulas) can improve nutrient intake and promote anabolism in critically ill infants. However, the effect of increased protein and energy intake on arginine metabolism is not known.

OBJECTIVE

We investigated the effect of a PE-formula compared with that of a standard infant formula (S-formula) on arginine kinetics in critically ill infants.

DESIGN

A 2-h stable-isotope tracer protocol was conducted in 2 groups of critically ill infants with respiratory failure because of viral bronchiolitis, who received either a PE-formula (n = 8) or S-formula (n = 10) in a randomized, blinded, controlled setting. Data were reported as means ± SDs.

RESULTS

The intake of a PE-formula in critically ill infants (aged 0.23 ± 0.14 y) resulted in an increased arginine appearance (PE-formula: 248 ± 114 μmol · kg(-1) · h(-1); S-formula: 130 ± 53 μmol · kg(-1) · h(-1); P = 0.012) and NO synthesis (PE-formula: 1.92 ± 0.99 μmol · kg(-1) · h(-1); S-formula: 0.84 ± 0.36 μmol · kg(-1) · h(-1); P = 0.003), whereas citrulline production and plasma arginine concentrations were unaffected.

CONCLUSION

In critically ill infants with respiratory failure because of viral bronchiolitis, the intake of a PE-formula increases arginine availability by increasing arginine appearance, which leads to increased NO synthesis, independent of plasma arginine concentrations. This trial was registered at www.trialregister.nl as NTR515.

摘要

背景

精氨酸被认为是儿童危重病期间的必需氨基酸,补充精氨酸已被提议改善精氨酸的可用性,以促进一氧化氮(NO)的合成。富含蛋白质-能量的肠内配方(PE 配方)可以增加营养物质的摄入并促进危重症婴儿的合成代谢。然而,增加蛋白质和能量摄入对精氨酸代谢的影响尚不清楚。

目的

我们研究了与标准婴儿配方(S 配方)相比,PE 配方对患有病毒性毛细支气管炎导致呼吸衰竭的危重症婴儿精氨酸动力学的影响。

设计

在一组接受随机、盲法、对照研究的患有病毒性毛细支气管炎导致呼吸衰竭的危重症婴儿中,进行了 2 小时稳定同位素示踪剂方案,他们分别接受 PE 配方(n = 8)或 S 配方(n = 10)。数据以平均值 ± 标准差表示。

结果

PE 配方在接受治疗的危重症婴儿(年龄 0.23 ± 0.14 岁)中的摄入导致精氨酸出现增加(PE 配方:248 ± 114 μmol·kg-1·h-1;S 配方:130 ± 53 μmol·kg-1·h-1;P = 0.012)和一氧化氮合成增加(PE 配方:1.92 ± 0.99 μmol·kg-1·h-1;S 配方:0.84 ± 0.36 μmol·kg-1·h-1;P = 0.003),而瓜氨酸的产生和血浆精氨酸浓度不受影响。

结论

在患有病毒性毛细支气管炎导致呼吸衰竭的危重症婴儿中,PE 配方的摄入通过增加精氨酸的出现来增加精氨酸的可用性,从而增加一氧化氮的合成,而与血浆精氨酸浓度无关。该试验在 www.trialregister.nl 上注册为 NTR515。