首页> 外文学位 >Comparison of isotopic tracer techniques for measurement of whole body proteolysis in response to diet intervention and exercise training.
【24h】

Comparison of isotopic tracer techniques for measurement of whole body proteolysis in response to diet intervention and exercise training.

机译:比较同位素示踪技术测量饮食干预和运动训练引起的全身蛋白水解。

获取原文
获取原文并翻译 | 示例

摘要

Research employing simultaneous use of tracers has documented different findings dependent on the specific tracer, even when other study parameters remain constant. This line of inquiry is limited, especially with regard to comparisons between two of the tracers most commonly employed in assessment of protein breakdown: [2H5]-phenylalanine and [1- 13C]-leucine. This investigation consists of two studies which provide a direct comparison of these tracers in response to diet intervention and exercise training. In the first investigation, [2H5]-phenylalanine and [1-13C]-leucine were used to assess and compare rates of whole body proteolysis during recovery from an acute bout of exercise in male runners consuming eucaloric diets providing 3.6(HP), 1.8(MP), and 0.8(LP) g/kg/day of protein for 4 weeks. There was a significant increase (p0.05) in whole body proteolysis as assessed by [2H5]-phenylalanine and [1-13C]-leucine rates of appearance following an endurance exercise bout in these as athletes protein intakes increased. This showed similar changes in whole body proteolysis in response to habitual consumption of increased dietary protein following recovery from an acute bout of endurance exercise irrespective of the tracer.; In the second investigation, [2H5]-phenylalanine and [1-13C]-leucine kinetics, as well as the single and reciprocal pool models of leucine kinetics were used to assess and compare rates of whole body protein breakdown following 4 weeks of an aerobic exercise training in healthy, weight stable individuals consuming 0.8g/kg/day of protein. Aerobic exercise training increased whole body protein breakdown according to estimates based on [1-13C]-leucine rate of appearance, while exercise training had no effect on proteolysis when [2H5]-phenylalanine kinetics were applied. Single and reciprocal pool estimates both documented a decrease in whole body proteolysis posttraining, while only the reciprocal pool detected a decrease in leucine oxidation. This study highlights the impact choice of isotopic tracer and subsequent modeling has on research findings derived from studies seeking to characterize the effects of chronic endurance exercise on whole body protein breakdown.; Future research is warranted to investigate similarities and discrepancies that occur when simultaneously employing multiple isotopic tracers and/or models. Studies designed to test for differences between isotopic tracers and/or models in response to interventions would provide key insight into factors that contribute to discrepancies between tracers and/or models. Research designed to investigate the mechanisms that cause estimates of whole body protein breakdown to differ between tracers and/or models would help researchers design studies aimed to specifically capture treatment effects independent of validity of assumptions specific to and required for isotope modeling studies.
机译:同时使用示踪剂的研究已记录了取决于特定示踪剂的不同发现,即使其他研究参数保持不变也是如此。这条查询线是有局限性的,特别是在比较两个最常用于评估蛋白质分解的示踪剂之间的比较方面:[2H5]-苯丙氨酸和[1-13C]-亮氨酸。这项调查包括两项研究,这些研究提供了对这些示踪剂进行饮食干预和运动训练的直接比较。在第一个研究中,[2H5]-苯丙氨酸和[1-13C]-亮氨酸被用于评估和比较男性饮食者在从急速运动中恢复时全身蛋白水解的速率,这些男性跑步者服用了提供3.6(HP),1.8的桉树饮食(MP)和0.8(LP)g / kg /天的蛋白质,持续4周。在耐力运动后,随着运动员蛋白质摄入量的增加,通过[2H5]-苯丙氨酸和[1-13C]-亮氨酸的出现率评估,全身蛋白水解显着增加(p <0.05)。这表明,从急性耐力运动恢复后,不管蛋白示踪剂如何,人体对日常饮食中增加的饮食蛋白质摄入量增加后,全身蛋白水解的变化都相似。在第二项研究中,使用[2H5]-苯丙氨酸和[1-13C]-亮氨酸动力学以及亮氨酸动力学的单池模型和倒数池模型来评估和比较有氧运动4周后全身蛋白质分解的速率在体重为0.8g / kg /天的健康,体重稳定的个体中进行运动训练。根据基于[1-13C]-亮氨酸出现率的估计,有氧运动训练增加了全身蛋白质分解,而当应用[2H5]-苯丙氨酸动力学时,运动训练对蛋白水解没有影响。单个和倒数池估计都记录了全身蛋白水解后训练的减少,而只有倒数池检测到亮氨酸氧化的减少。这项研究强调了同位素示踪剂的影响选择,随后的建模对旨在表征慢性耐力运动对全身蛋白质分解的影响的研究得出的研究结果具有重要意义。有必要进行进一步的研究来调查同时使用多个同位素示踪剂和/或模型时发生的相似性和差异。旨在测试同位素示踪剂和/或模型之间的差异以响应干预措施的研究将提供对导致示踪剂和/或模型之间差异的因素的关键见解。旨在调查导致全身蛋白质分解估计值在示踪剂和/或模型之间不同的机制的研究,将有助于研究人员设计旨在专门捕获治疗效果的研究,而与特定于同位素建模研究的假设的有效性无关。

著录项

  • 作者

    Martin, William Forrest.;

  • 作者单位

    University of Connecticut.;

  • 授予单位 University of Connecticut.;
  • 学科 Health Sciences Nutrition.; Chemistry Biochemistry.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 181 p.
  • 总页数 181
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 预防医学、卫生学 ; 生物化学 ;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号