Nasogastric bolus administration of a protein-rich drink augments insulinaemia and aminoacidaemia but not whole-body protein turnover or muscle protein synthesis versus oral administration.

IF 6.7 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Clinical science Pub Date : 2024-01-10 DOI:10.1042/CS20231126
George F Pavis, Doaa R Abdelrahman, Andrew J Murton, Benjamin T Wall, Francis B Stephens, Marlou L Dirks
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Abstract

Nasogastric feeding of protein-rich liquids is a nutritional support therapy that attenuates muscle mass loss. However, whether administration via a nasogastric tube per se augments whole-body or muscle protein anabolism compared with oral administration is unknown. Healthy participants were administered a protein-rich drink (225 ml containing 21 g protein) orally (ORAL; n=13; age 21 ± 1 year; BMI 22.2 ± 0.6 kg·m-2) or via a nasogastric tube (NG; n=13; age 21 ± 1 yr; BMI 23.9 ± 0.9 kg·m-2) in a parallel group design, balanced for sex. L-[ring-2H5]-phenylalanine and L-[3,3-2H2]-tyrosine were infused to measure postabsorptive and postprandial whole-body protein turnover. Skeletal muscle biopsies were collected at -120, 0, 120 and 300 min relative to drink administration to quantify temporal myofibrillar fractional synthetic rates (myoFSR). Drink administration increased serum insulin and plasma amino acid concentrations, and to a greater extent and duration in NG versus ORAL (all interactions P<0.05). Drink administration increased whole-body protein synthesis (P<0.01), suppressed protein breakdown (P<0.001), and created positive net protein balance (P<0.001), but to a similar degree in ORAL and NG (interactions P>0.05). Drink administration increased myoFSR from the postabsorptive state (P<0.01), regardless of route of administration in ORAL and in NG (interaction P>0.05). Nasogastric bolus administration of a protein-rich drink induces insulinaemia and aminoacidaemia to a greater extent than oral administration, but the postprandial increase in whole-body protein turnover and muscle protein synthesis was equivalent between administration routes. Nasogastric administration is a potent intervention to increase postprandial amino acid availability. Future work should assess its utility in overcoming impaired sensitivity to protein feeding, such as that seen in ageing, disuse, and critical care.

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与口服给药相比,鼻饲蛋白质给药能增强胰岛素血症和氨基酸血症,但不能增强全身蛋白质周转或肌肉蛋白质合成。
鼻饲富含蛋白质的液体是一种营养支持疗法,可减轻肌肉质量的损失。然而,与口服相比,通过鼻胃管给药本身是否能促进全身或肌肉蛋白质合成代谢尚不清楚。在平行分组设计中,健康参与者口服(ORAL;n=13;年龄 21±1岁;体重指数 22.2±0.6 kg-m-2)或通过鼻胃管(NG;32 n=13;年龄 21±1岁;体重指数 23.9±0.9 kg-m-2)摄入富含蛋白质的饮料(225 mL,含 21 g 蛋白质),性别平衡。输注 L-[环-2H5]-苯丙氨酸和 L-[3,3-2H2]-酪氨酸以测量吸收后和餐后全身蛋白质周转。在给药后 -120 分钟、0 分钟、120 分钟和 300 分钟采集骨骼肌活检,以量化时间性肌纤维部分合成率(myoFSR)。饮用饮料会增加血清胰岛素和血浆氨基酸浓度,NG 与口服相比,浓度增加的程度更大,持续时间更长(所有交互作用均为 P0.05)。从吸收后状态开始,给药会增加肌FSR(P0.05)。鼻饲给药比口服给药更能诱导胰岛素血症和氨基酪氨酸血症,但两种给药途径餐后全身蛋白质周转和肌肉蛋白质合成的增加是相同的。鼻胃给药是增加餐后氨基酸供应的有效干预措施。未来的工作应评估其在克服蛋白质喂养敏感性受损方面的作用,如在老龄化、废用症和重症监护中出现的情况。
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来源期刊
Clinical science
Clinical science 医学-医学:研究与实验
CiteScore
11.40
自引率
0.00%
发文量
189
审稿时长
4-8 weeks
期刊介绍: Translating molecular bioscience and experimental research into medical insights, Clinical Science offers multi-disciplinary coverage and clinical perspectives to advance human health. Its international Editorial Board is charged with selecting peer-reviewed original papers of the highest scientific merit covering the broad spectrum of biomedical specialities including, although not exclusively: Cardiovascular system Cerebrovascular system Gastrointestinal tract and liver Genomic medicine Infection and immunity Inflammation Oncology Metabolism Endocrinology and nutrition Nephrology Circulation Respiratory system Vascular biology Molecular pathology.
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