Divergent serum metabolomic, skeletal muscle signaling, transcriptomic, and performance adaptations to fasted versus whey protein-fed sprint interval training

被引:11
|
作者
Aird, Tom P. [1 ,2 ]
Farquharson, Andrew J. [3 ]
Bermingham, Kate M. [4 ]
O'Sulllivan, Aifric [4 ]
Drew, Janice E. [3 ]
Carson, Brian P. [1 ,2 ]
机构
[1] Univ Limerick, Phys Educ & Sports Sci, Limerick, Ireland
[2] Univ Limerick, Hlth Res Inst, Phys Act Hlth, Limerick, Ireland
[3] Univ Aberdeen, Rowett Inst, Aberdeen, Scotland
[4] Univ Coll Dublin, Sch Agr & Food Sci, Dublin, Ireland
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2021年 / 321卷 / 06期
关键词
exercise performance; mitochondrial biogenesis; skeletal muscle metabolism; whey protein; REDUCED CARBOHYDRATE AVAILABILITY; FATTY-ACID OXIDATION; MITOCHONDRIAL BIOGENESIS; EXERCISE PERFORMANCE; ENDURANCE EXERCISE; GLUCOSE-INGESTION; GENE-EXPRESSION; FUEL SELECTION; AMINO-ACIDS; RESPONSES;
D O I
10.1152/ajpendo.00265.2021
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sprint interval training (SIT) is a time-efficient alternative to endurance exercise, conferring beneficial skeletal muscle metabolic adaptations. Current literature has investigated the nutritional regulation of acute and chronic exercise-induced metabolic adaptations in muscle following endurance exercise, principally comparing the impact of training in fasted and carbohydrate-fed (CHO) conditions. Alternative strategies such as exercising in low CHO, protein-fed conditions remain poorly characterized, specifically pertaining to adaptations associated with SIT. Thus, this study aimed to compare the metabolic and performance adaptations to acute and short-term SIT in the fasted state with preexercise hydrolyzed (WPH) or concentrated (WPC) whey protein supplementation. In healthy males, preexercise protein ingestion did not alter exercise-induced increases in PGC-1 alpha, PDK4, SIRT1, and PPAR-delta mRNA expression following acute SIT. However, supplementation of WPH beneficially altered acute exercise-induced CD36 mRNA expression. Preexercise protein ingestion attenuated acute exercise-induced increases in muscle pan-acetylation and PARP1 protein content compared with fasted SIT. Acute serum metabolomic differences confirmed greater preexercise amino acid delivery in protein-fed compared with fasted conditions. Following 3 wk of SIT, training-induced increases in mitochondrial enzymatic activity and exercise performance were similar across nutritional groups. Interestingly, resting muscle acetylation status was downregulated in WPH conditions following training. Such findings suggest preexercise WPC and WPH ingestion positively influences metabolic adaptations to SIT compared with fasted training, resulting in either similar or enhanced performance adaptations. Future studies investigating nutritional modulation of metabolic adaptations to exercise are warranted to build upon these novel findings. NEW & NOTEWORTHY These are the first data to show the influence of preexercise protein on serum and skeletal muscle metabolic adaptations to acute and short-term sprint interval training (SIT). Preexercise whey protein concentrate (WPC) or hydrolysate (WPH) feeding acutely affected the serum metabolome, which differentially influenced acute and chronic changes in mitochondrial gene expression, intracellular signaling (acetylation and PARylation) resulting in either similar or enhanced performance outcomes when compared with fasted training.
引用
收藏
页码:E802 / E820
页数:19
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