在分解代谢状态下使用合成代谢剂。

Journal of burns and wounds Pub Date : 2007-02-12
Robert Demling
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引用次数: 0

摘要

目的:我们计划回顾目前由损伤和危重症引起的分解代谢状态下的瘦物质侵蚀问题。这种蛋白质损失是由激素失衡和过度炎症引起的,称为“损伤应激反应”。然后,我们计划提供关于使用可用合成代谢剂来减弱过度分解代谢的当前概念。数据来源:综述了关于急性分解代谢状态的发病机制、合成代谢和抗代谢药物的使用、适应症、作用机制和潜在并发症的现有已发表文献。数据提取:描述了目前对可用的合成代谢剂和抗合成代谢剂的理解和经验,以及每种合成代谢剂使用的基本原理。结论:我们得出的结论是,在重症监护人群的管理中,保持瘦体重(身体蛋白)极其重要,因为瘦体重的减少会导致严重的发病率和死亡率增加。从本质上讲,所有可用的合成代谢剂都能刺激蛋白质合成并减少蛋白质分解,但都有不同的作用机制。充足的营养,尤其是蛋白质的摄入,对于任何合成代谢的发生都是至关重要的。联合合成代谢疗法似乎也是有利的。尽管控制炎症反应对进一步控制蛋白质损失也有重大益处,但有效和安全的抗炎剂尚未在临床上用于此目的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The use of anabolic agents in catabolic states.

Objective: We plan to review the current problem of lean mass erosion in catabolic states, caused by injury and critical illness. This protein loss is driven by the hormonal imbalance and excess inflammation referred to as the "stress response to injury." We then plan to provide the current concepts on the use of available anabolic agents to attenuate the excess catabolism.

Data source: The available published literature on the pathogenesis of acute catabolic states and the use of anabolic and anticatabolic agents, their indications, mechanism of action, and potential complications was reviewed.

Data extraction: The current understanding and experience of the available anabolic and anticatabolic agents as well as the rationale for the use of each anabolic agent are described.

Conclusion: We conclude that the preservation of lean body mass (body protein) is extremely important in the management of critical care populations, as lean mass loss leads to severe morbidity and increased mortality. Essentially, all of the available anabolic agents stimulate protein synthesis and decrease protein breakdown, but all have different mechanisms of action. Adequate nutrition, especially protein intake, is essential for any anabolism to occur. Combined anabolic therapy also appears to be advantageous. Although controlling the inflammatory response would also be of major benefit in further controlling protein loss, effective and safe anti-inflammatory agents have not yet become clinically available for this purpose.

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