Sacks G S
Department of Clinical Pharmacy Practice, University of Mississippi Medical Center, Jackson 39216, USA.
Ann Pharmacother. 1999 Mar;33(3):348-54. doi: 10.1345/aph.18200.
To evaluate the safety and efficacy of parenteral and enteral glutamine supplementation in patients who are catabolic.
English-language clinical trials and review articles identified by MEDLINE searches (January 1970-December 1997) and from bibliographies of selected articles were considered for possible inclusion. Key words used in the search strategy were glutamine, critical illness, stress, catabolism, injury, enteral nutrition, and parenteral nutrition.
Inclusion was restricted to pertinent studies that evaluated the safety of glutamine supplementation, as well as effects of glutamine on amino acid metabolism, immune function, and patient outcome. Data from 18 clinical trials and multiple review articles were compiled into a review format.
Glutamine is an important metabolic fuel for intestinal enterocytes, lymphocytes and macrophages, and metabolic precursors such as purines and pyrimidines. Although originally considered a nonessential amino acid, experimental work suggests that glutamine is essential for maintaining intestinal function, immune response, and amino acid homeostasis during periods of severe stress. In the past decade, clinical trials conducted in metabolically stressed patients indicate that glutamine improves nitrogen balance, increases cellular proliferation, decreases the incidence of infection, and shortens hospital stay in some catabolic patients.
Glutamine has been studied extensively over the past decade for its role during critical illness. Clinical trials conducted in humans demonstrate glutamine to be well tolerated without adverse consequences, even during times of stress. Although glutamine has shown promise in select groups of catabolic patients, additional studies are needed to define which patient populations derive the greatest benefit from supplemental glutamine and the mechanisms by which these effects are exerted.
评估胃肠外和胃肠内补充谷氨酰胺对分解代谢患者的安全性和有效性。
通过MEDLINE检索(1970年1月至1997年12月)确定的英文临床试验和综述文章,并考虑从所选文章的参考文献中获取可能纳入的内容。检索策略中使用的关键词为谷氨酰胺、危重病、应激、分解代谢、损伤、肠内营养和胃肠外营养。
纳入仅限于评估补充谷氨酰胺的安全性以及谷氨酰胺对氨基酸代谢、免疫功能和患者结局影响的相关研究。将来自18项临床试验和多篇综述文章的数据整理成综述形式。
谷氨酰胺是肠上皮细胞、淋巴细胞和巨噬细胞重要的代谢燃料,也是嘌呤和嘧啶等代谢前体。尽管谷氨酰胺最初被认为是非必需氨基酸,但实验研究表明,在严重应激期间,谷氨酰胺对于维持肠道功能、免疫反应和氨基酸稳态至关重要。在过去十年中,对处于代谢应激状态患者进行的临床试验表明,谷氨酰胺可改善氮平衡、增加细胞增殖、降低感染发生率,并缩短部分分解代谢患者的住院时间。
在过去十年中,对谷氨酰胺在危重病期间的作用进行了广泛研究。在人体中进行的临床试验表明,即使在应激期间,谷氨酰胺也具有良好的耐受性,无不良后果。尽管谷氨酰胺在部分分解代谢患者组中显示出前景,但仍需要进一步研究来确定哪些患者群体从补充谷氨酰胺中获益最大以及产生这些作用的机制。