Clinical Medical Research Center, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing China.
Institute of Burn Research, State Key Laboratory of Trauma, Burns and Combined Injury, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing China.
Nutrition. 2020 Nov-Dec;79-80:110934. doi: 10.1016/j.nut.2020.110934. Epub 2020 Jul 3.
This study aimed to explore the effects of glutamine on hypermetabolic reactions in burned rats and its underlying mechanism.
Fifty-five Sprague-Dawley rats were randomly divided into three groups, namely, the control (C), burned (B), and burned + glutamine (B + G) groups. Rats in the glutamine treatment group were supplemented with 1 g glutamine per kg body weight. Changes in body weight and resting energy expenditure in all groups were observed daily. Blood glucose and glucose tolerance level were measured on days 1, 3, 7, 10 and 14 after burn injury. On days 7 and 14 after injury, the rats were sacrificed, and the weight and protein content of the skeletal muscle were measured. Moreover, the level of glutamine, inflammatory mediator, nicotinamide adenine dinucleotide phosphate (NADPH), glutathione, and the activity of glutamine metabolic enzymes were measured.
The hypermetabolic reaction after burn injury was significantly inhibited by glutamine administration, and the range of variations in the resting energy expenditure and body weight indicators was narrowed remarkably (P < 0.05 or 0.01), whereas the weight and protein content of the skeletal muscle returned to normal (P < 0.05 or 0.01). Glutamine could increase glutaminase activity in various tissues, promote the utilization of glutamine, and appropriately reduce the degree of organ damage and inflammatory response (P < 0.05 or 0.01). Furthermore, glutamine could promote the synthesis of the reducing substances NADPH and glutathione (P < 0.05 or 0.01).
Glutamine administration effectively reduces hypermetabolic reactions by promoting NADPH synthesis, inhibiting oxidative stress, and improving glutamine utilization after burn injury.
本研究旨在探讨谷氨酰胺对烧伤大鼠高代谢反应的影响及其作用机制。
将 55 只 Sprague-Dawley 大鼠随机分为三组,即对照组(C)、烧伤组(B)和烧伤+谷氨酰胺组(B+G)。谷氨酰胺治疗组大鼠补充 1 g/kg 体重的谷氨酰胺。观察各组大鼠的体重和静息能量消耗的变化。烧伤后第 1、3、7、10 和 14 天测量血糖和葡萄糖耐量水平。烧伤后第 7 和 14 天处死大鼠,测量骨骼肌重量和蛋白质含量。此外,还测量了谷氨酰胺、炎症介质、烟酰胺腺嘌呤二核苷酸磷酸(NADPH)、谷胱甘肽和谷氨酰胺代谢酶的活性。
谷氨酰胺给药显著抑制烧伤后的高代谢反应,显著缩小静息能量消耗和体重指标的变化范围(P<0.05 或 0.01),骨骼肌重量和蛋白质含量恢复正常(P<0.05 或 0.01)。谷氨酰胺可以增加各种组织中的谷氨酰胺酶活性,促进谷氨酰胺的利用,适当减轻器官损伤和炎症反应的程度(P<0.05 或 0.01)。此外,谷氨酰胺可以促进还原物质 NADPH 和谷胱甘肽的合成(P<0.05 或 0.01)。
谷氨酰胺给药通过促进 NADPH 合成、抑制氧化应激和改善烧伤后谷氨酰胺的利用,有效减轻高代谢反应。