Osowska Sylwia, De Bandt Jean-Pascal, Chaïb Samira, Neveux Nathalie, Bérard Marie-Pierre, Cynober Luc
Laboratoire de Biologie de la Nutrition, Faculté de Pharmacie, Université Paris 5, 75270 Paris 06, France.
Intensive Care Med. 2003 Oct;29(10):1798-801. doi: 10.1007/s00134-003-1878-9. Epub 2003 Jul 17.
As is the case with glutamine, requirements for amino acids such as cysteine, taurine, and serine may be increased in stress situations. This study evaluated the potential usefulness of supplementation of total parenteral nutrition with a cysteine, taurine, threonine, and serine mixture (SEAS), with or without glutamine, in an experimental model of turpentine-induced acute inflammation.
Prospective, controlled animal study in male Sprague-Dawley rats.
Twenty-seven rats received isonitrogenous, isocaloric total parenteral nutrition (260 kcal/kg, 2 gN/kg per day) for 5 days. They were divided into three groups according to the composition of the amino acid admixture: standard amino acids (control, n=9), standard amino acids partly substituted with SEAS (n=10) or with SEAS and glutamine (n=8). All rats received two subcutaneous turpentine injections (0.5 ml/100 g) 24 h (day 2) and 72 h (day 4) after the initiation of parenteral nutrition and were killed on day 5.
Nitrogen balance was significantly increased (control 53+/-29, SEAS 153+/-21, SEAS+Gln 187+/-32 mg/24 h) and urinary 3-methylhistidine/creatinine ratio decreased (control 55+/-4, SEAS 43+/-4, SEAS+Gln 38+/-3 micro mol/mmol) on day 5 in the two SEAS-treated groups. Hepatic and extensor digitorum longus muscle protein contents were significantly higher in the SEAS+Gln-treated group than in the other two groups. In addition to slight differences in liver amino acid content, other parameters including liver glutathione did not differ significantly between groups.
Improved nitrogen balance and reduction in urinary 3-methylhistidine suggest that SEAS supplementation improves nitrogen homeostasis in an experimental model of acute inflammation. Glutamine addition further improves protein status.
与谷氨酰胺的情况一样,在应激状态下,对半胱氨酸、牛磺酸和丝氨酸等氨基酸的需求可能会增加。本研究在松节油诱导的急性炎症实验模型中,评估了添加或不添加谷氨酰胺的半胱氨酸、牛磺酸、苏氨酸和丝氨酸混合物(SEAS)补充全肠外营养的潜在效用。
对雄性Sprague-Dawley大鼠进行的前瞻性对照动物研究。
27只大鼠接受等氮、等热量的全肠外营养(260千卡/千克,2克氮/千克/天),持续5天。根据氨基酸混合物的组成将它们分为三组:标准氨基酸组(对照组,n = 9)、部分用SEAS替代标准氨基酸的组(n = 10)或用SEAS和谷氨酰胺替代的组(n = 8)。所有大鼠在肠外营养开始后24小时(第2天)和72小时(第4天)接受两次皮下注射松节油(0.5毫升/100克),并在第5天处死。
在第5天,两个SEAS治疗组的氮平衡显著增加(对照组53±29,SEAS组153±21,SEAS +谷氨酰胺组187±32毫克/24小时),尿3-甲基组氨酸/肌酐比值降低(对照组55±4,SEAS组43±4,SEAS +谷氨酰胺组38±3微摩尔/毫摩尔)。SEAS +谷氨酰胺治疗组的肝脏和趾长伸肌蛋白质含量显著高于其他两组。除肝脏氨基酸含量存在细微差异外,包括肝脏谷胱甘肽在内的其他参数在各组之间无显著差异。
氮平衡改善和尿3-甲基组氨酸减少表明,在急性炎症实验模型中,补充SEAS可改善氮稳态。添加谷氨酰胺可进一步改善蛋白质状态。