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Supplementation Trial on Arginine With Metabolic Profiling

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赞助商
Pennington Biomedical Research Center
合作者
Jennifer C. Rood
Robbie A. Beyl
Corby K. Martin
Frank L. Greenway

关键词

抽象

This study will assess effects of an acute dose of the amino acid arginine on metabolism in healthy young men.

描述

A double - blind randomized, crossover design trial examining arginine vs. placebo beverage treatments will be performed. The primary objective is to determine the effects of arginine assessed by standard laboratory assays and metabolomics. To accomplish the objective standardized meals will be provided for 2 days preceding treatment for dietary consistency. Participants will arrive at the center following a 10-12 hr fast. Blood samples will be collected at baseline (fasting), 1.5 hrs, 3.0 hrs, 6.0 hrs, and 24 hrs post treatment. Plasma prolactin, growth hormone, amino acids, glucose, insulin, triacylglycerols, thyroid hormones (TSH, T3, and T4), sex hormone binding globulin (SHBH), testosterone, cortisol, DHEA, and citrulline will be measured. Metabolomics will be measured at 3 time points for each treatment. Peripheral arterial tonometry (PAT) will also be performed at ~2 hrs following treatment to examine endothelial function in response to nitrous oxide release. In addition, psychological status including fatigue will be assessed using a standardized mood questionnaire (POMS).

日期

最后验证: 07/31/2019
首次提交: 01/10/2018
提交的预估入学人数: 01/16/2018
首次发布: 01/23/2018
上次提交的更新: 08/25/2019
最近更新发布: 08/27/2019
实际学习开始日期: 02/07/2018
预计主要完成日期: 07/07/2019
预计完成日期: 12/14/2019

状况或疾病

Protein
Amino Acid
Arginine

干预/治疗

Dietary Supplement: Arginine

Dietary Supplement: Placebo

-

手臂组

干预/治疗
Experimental: Arginine
Arginine drink provided 1 time. There is about 10 g of arginine in the product.
Dietary Supplement: Arginine
10 g of arginine in a formulated drink
Placebo Comparator: Placebo
Placebo drink provided 1 time.
Dietary Supplement: Placebo
formulated drink

资格标准

有资格学习的年龄 18 Years 至 18 Years
有资格学习的性别Male
接受健康志愿者
标准

Inclusion Criteria:

- BMI 18.5 - 25 kg/m2.

- Must be physically active (exercise at least 2 days/week).

- Willing to refrain from alcohol and supplements for the duration of the study.

- Willing to refrain from supplement ingestion, nuts, watermelon, and cracklins (fatback) for the 2 weeks prior to the initial treatment diet through the duration of the study.

Exclusion Criteria:

- HIV or AIDS

- Uncontrolled CVD/arrhythmia

- Type I or type II diabetes

- Pregnancy (or breastfeeding)

- Diagnosed eating disorder

- Non-normal sleeping patterns

- Chronic neurological condition

- Altered metabolism including growth hormone disorders

- Use of nicotine or tobacco products

- Heavy caffeine use (≥ 350 mg caffeine/d)

- Whole blood donation within previous eight weeks

- Protein supplementation

- Protein wasting disease.

- Exclusionary medications include diuretics, beta-blockers, weight loss medications or diet pills, anti-inflammatory drugs (corticosteroid/ anabolic steroid/NSAID), antipsychotic medication or other medication that may affect fluid balance, metabolism, or body weight.

- Prisoners and adults who are unable to consent will be excluded from the study.

- Lastly any other medical, psychiatric, or behavioral factors in the judgement of the Principle Investigator that may interfere with study participation or the ability to follow the protocol.

结果

主要结果指标

1. Growth Hormone [baseline (fasting), 1.5, 3.0, 6.0, and 24.0 hrs]

Change in GH

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