Tsuei Betty J, Bernard Andrew C, Barksdale Andrew R, Rockich Anna K, Meier Cynthia F, Kearney Paul A
Department of Surgery, University of Kentucky, Lexington, Kentucky 40536-0293, USA.
J Surg Res. 2005 Jan;123(1):17-24. doi: 10.1016/j.jss.2004.07.006.
Arginine has been added to immune enhancing diets that may improve patient outcomes, but little is known about the metabolic fate of supplemental arginine. We hypothesize that supplemental enteral arginine in injured patients is metabolized to ornithine by increased activity of the enzyme arginase.
Twenty-five adult patients with injury severity scores > or =20 received up to 14 days of enteral nutrition supplemented with arginine (30 g/day) or placebo in a prospective, randomized, blinded study. Plasma arginine, citrulline, and ornithine concentrations and peripheral blood mononuclear cell (PBMC) arginase activity were measured at baseline and on days 1, 3, 5, 7, 10, and 14. Clinical data collected included demographics, injury patterns, lengths of stay, and infectious complications. Data were analyzed using ANOVA and t test.
PBMC arginase activity was elevated in all patients. In the supplemented group, plasma arginine concentrations increased at days 7, 10, and 14 when compared to baseline (P < 0.05) and were higher at day 14 when compared to those of controls (P < 0.05). Citrulline concentrations in both groups were unchanged over time. Ornithine concentration increased within 24 h of arginine supplementation and remained elevated when compared to baseline (P < 0.01). Ornithine concentration in the supplemented group was higher at days 1, 3, 5, and 7 when compared to that of controls (P < 0.05). There were no differences in clinical outcomes.
Supplemental enteral arginine is absorbed in injured patients and increases arginine levels. Supplemental arginine appears to be metabolized to ornithine. Increased arginase enzyme activity in peripheral blood mononuclear cells may be a contributor.
精氨酸已被添加到免疫增强饮食中,这可能改善患者预后,但对于补充精氨酸的代谢去向知之甚少。我们推测,在受伤患者中,补充的肠内精氨酸通过精氨酸酶活性增加而代谢为鸟氨酸。
在一项前瞻性、随机、双盲研究中,25名损伤严重程度评分≥20的成年患者接受了长达14天的补充精氨酸(30克/天)或安慰剂的肠内营养。在基线以及第1、3、5、7、10和14天测量血浆精氨酸、瓜氨酸和鸟氨酸浓度以及外周血单核细胞(PBMC)精氨酸酶活性。收集的临床数据包括人口统计学、损伤类型、住院时间和感染并发症。使用方差分析和t检验分析数据。
所有患者的PBMC精氨酸酶活性均升高。在补充组中,与基线相比,血浆精氨酸浓度在第7、10和14天升高(P<0.05),与对照组相比,在第14天更高(P<0.05)。两组中的瓜氨酸浓度随时间未发生变化。鸟氨酸浓度在补充精氨酸后24小时内升高,与基线相比仍保持升高(P<0.01)。与对照组相比,补充组中的鸟氨酸浓度在第1、3、5和7天更高(P<0.05)。临床结局无差异。
补充的肠内精氨酸在受伤患者中被吸收并提高了精氨酸水平。补充的精氨酸似乎代谢为鸟氨酸。外周血单核细胞中精氨酸酶活性增加可能是一个促成因素。