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临床试验/NCT04887727
NCT04887727已完成不适用

Development of Oral Amino Acid Tracers to Study Protein Turnover in Humans

University of Toronto2 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2019年2月25日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
22
试验地点
2
主要终点
Myofibrillar protein synthesis rates

研究概览

简要总结

Previous studies have used a combination of oral L-[1-13C]leucine and intravenous labeled L-[5,5,5-2H3]leucine to assess the acute postprandial changes in whole-body protein turnover (12, 19). Intravenous and dietary-labeled amino acid tracers have also been used in tandem to assess rates of myofibrillar protein synthesis in response to bolus protein ingestion and resistance exercise (46). By validating whole-body net balance to myofibrillar protein synthesis, our proposed multi-tracer approach will develop minimally invasive models to study protein turnover in a variety of populations in which traditional infusions and/or repeated blood samples are not possible (i.e. pediatric, free-living populations).

详细描述

The primary objective of the proposed study is to validate the use of a novel oral tracer model to accurately and reliably measure myofibrillar protein synthesis. It is hypothesized that oral L-[1-13C]leucine and L-[ring-2H5]phenylalanine, ingested as a bolus to mimic an intravenous 'pulse dose' administration (51, 65), will reveal similar rates of myofibrillar protein synthesis when compared to traditional intravenous L-[5,5,5-2H3]leucine infusion. Moreover, it is hypothesized that both methods will reveal the expected graded changes in myofibrillar protein synthesis in response to feeding and resistance exercise (i.e. fasted<feeding<exercise & feeding).

The secondary objective of the proposed study is to develop and validate non-invasive models to measure whole-body amino acid oxidation and net balance in response to feeding and resistance exercise. It is hypothesized that whole-body net balance, as determined by a novel oral tracer model (i.e. L-[1-13C]leucine) , will align with traditional intravenous tracer methodology (i.e. L-[5,5,5-2H3]leucine) and reveal the expected physiological changes in whole-body protein turnover in response to feeding and resistance exercise (i.e. fasted<feeding<exercise & feeding).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Currently performing structured physical activity 2-5 days per week

排除标准

  • Unable to safely perform exercise as per PARQ+ guidelines
  • Currently using tobacco products
  • Currently using or have history of anabolic steroid use
  • Diagnosed with medical condition including type 2 diabetes, cancer, heart disease
  • Unable to abstain from supplement use (HMB, branched chain amino acids, phosphatidic acid) for at least three weeks prior to trial
  • currently using medications known to affect protein metabolism e.g. corticosteroids, NSAID, prescription-strength acne medication
  • allergic to local anesthetics
  • female: Hormonal fluctuations associated with the menstrual cycle have been reported to alter protein metabolism during exercise and may influence indices of the post-exercise myofibrillar protein synthetic response. Accordingly, the study will include males to ensure a stable hormonal environment and to increase the homogeneity of the physiological response.

结局指标

主要结局

Myofibrillar protein synthesis rates

时间窗: 5 hours

Myofibrillar protein synthesis rates assessed by oral and intravenous tracers during Fast, Fed, and Ex-Fed

次要结局

  • Muscle anabolic signalling(2 and 5 hours)
  • Whole-body protein turnover(5 hours)
  • Amino acid oxidation and net protein balance(5 hours)
  • Amino acid transporter expression(2 and 5 hours)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Daniel Moore

Associate Professor

University of Toronto

研究点 (2)

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