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临床试验/NCT06781723
NCT06781723已完成不适用

Improving the Anabolic Action of Plant-based Foods Using Complementary Proteins

University of Illinois at Urbana-Champaign1 个研究点 分布在 1 个国家目标入组 11 人开始时间: 2024年9月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
11
试验地点
1
主要终点
Myofibrillar protein fractional synthesis rate

研究概览

简要总结

In a crossover design 10 young healthy adults (20-35 y) will receive stable isotope tracer infusions and perform a single bout of resistance exercise. Immediately after exercise participants will ingest either 246 g of rice and beans or its constituent macronutrients as isolated amino acids, carbohydrates, fiber, and fat. Repeated blood and muscle biopsies will be collected to determine amino acid concentrations, anabolic signaling and myofibrillar protein synthesis rates during the trials.

详细描述

  1. Preliminary Testing Preparation: Participants will arrive for the preliminary testing session after an overnight fast (~10 h no caloric foods/beverages consumed) and having refrained from exercise for the 72 h prior. Prior to any in-person procedures, participants will be briefed on the procedures and risks associated with participation via reviewing the informed consent document. Participants will be encouraged to ask questions and have their questions answered prior to being asked if they'd like to continue. Confirmation will be documented via signature on an informed consent process form.

1.1 Anthropometrics: Upon provision of consent, participants' height and weight will be measured to confirm body mass index (BMI) is within eligibility limits (18.5 - 30 kg/m^2). Since participants have already been assessed for all other inclusion and exclusion criteria, an eligible BMI will result in study inclusion and continuation of the preliminary testing session. Following confirmation of study eligibility, blood pressure will be measured by a trained member of the research team. Subsequently, body composition will be determined via dual energy x-ray absorptiometry (DEXA) in accordance with manufacturer recommendations. Briefly, participants will be asked to remove all metal objects from their person prior to being positioned by a trained technician for accurate measurement of lean body mass and fat mass. The scan lasts approximately 6-10 minutes during which the participant will be instructed to remain motionless.

1.2 Resting Metabolic Rate: Resting metabolic rate (RMR) will be assessed via indirect calorimetry. This is a non-exertional test whereby RMR is measured using an automated gas analysis system. This device measures oxygen consumption and carbon dioxide production as the difference between inspired and expired gas concentrations. Prior to the beginning of the test, participants will lie supine on a table and a clear, hard plastic hood and soft, clear plastic drape will be placed over the participants neck, head, and shoulders to capture expired gases. Participants will then lie motionless without falling asleep while respiratory gas concentrations are captured. Testing will conclude when RMR is stable for at least 20 min (typically ~30 min from the onset).

1.3 Ten-Repetition Maximum (10RM) Testing: Following resting metabolic rate testing, participants will have their 10RM tested for the leg extension and leg press. To begin, participants will cycle at a self-selected pace on a standard cycle ergometer for ~5 minutes. Participants will then complete a set of 8-10 repetitions at ~50% of their predicted 10RM followed by 1-2 minutes of rest. The load will then be set at ~90% of their predicted 10RM. Load will be increased by 2.5-5.0% following each successful attempt until failure (typically within 5 attempts). Two minutes of rest will be allotted between maximal attempts and 5 minutes between exercises. Leg extension will be tested first followed by leg press. Before leaving the laboratory, participants will be allowed to ask any questions they have before concluding the session.

1.4 Habitual Diet Record: Current diet intake will be assessed through an online automated self-administered (ASA24) diet record system. Participants will receive their individual and private username and password. They will be asked to record 3 consecutive days (2 weekdays, 1 weekend day). As it is an online system, they can complete off-site, at their leisure.

研究设计

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

入排标准

年龄范围
20 Years 至 35 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Age 20-35 yrs
  • •Pre-menopausal
  • •Recreationally-active
  • •Weight stable for prior 6 months

排除标准

  • •Age outside of range (20 - 35 yrs)
  • •Pregnancy
  • •Irregular menstrual cycles (i.e., ~21 day or ~35 day cycle)
  • •Participation in previous research using [13C6]phenylalanine
  • •Participation in other ongoing research that interferes with this study (e.g., conflicting diet, activity interventions, etc.)
  • •Any hospitalization or surgery for a metabolic, cardiovascular, or neuromusculoskeletal complication within the past year
  • •Allergy or hypersensitivity to local anesthetics, latex, or adhesives (bandages, medical tape, etc.)
  • •Excess scarring after injury
  • •History of excess bleeding after cut
  • •Chronic or frequent dizziness/fainting, and arm or leg weakness/numbness
  • •Arthritis
  • •Mental Illness
  • •Hepatorenal, cardiovascular musculoskeletal, autoimmune, or neurological disease or disorder
  • •Predisposition to hypertrophic scarring or keloid formation
  • •Physical activity limitations
  • •Consumption of ergogenic-levels of dietary supplements that may affect muscle mass (e.g., creatine, HMB), insulin-like substances, or anabolic/catabolic pro-hormones (e.g., DHEA) within 6 weeks prior to participation
  • •Consumption of thyroid, androgenic, or other medications known to affect endocrine function
  • •Consumption of medications known to affect protein metabolism (e.g., prescription-strength corticosteroids, non-steroidal anti-inflammatories, or acne medication)
  • •Unwillingness to comply with study procedures
  • •Weight unstable (variation >5% of bodyweight in last 6-12 months)
  • •Current or previous tobacco use with last 6 months
  • •Obesity (body mass index; BMI >>30 kg∙m^-2)
  • •Score of less than 14 on the Godin-Shephard Leisure-Time Physical Activity Questionnaire
  • •Phenylketonuria
  • •Anyone hospitalized previously for COVID-19 without a cardiovascular workup screening for cardiovascular issues post-infection
  • •Anyone recovering from COVID-19 infection within the preceding 10 days

研究组 & 干预措施

Rice and Beans (COMP)

Experimental

Rice and Beans

After resistance exercise, participants will ingest a meal of 123g Rice, 123g Black Beans (246 g; 575kcal, 20 g Protein, 121 g Carbohydrate, 0.7 g Fat, 1.78 g Fat)

干预措施: Resistance Exercise (Behavioral)

Rice and Beans (COMP)

Experimental

Rice and Beans

After resistance exercise, participants will ingest a meal of 123g Rice, 123g Black Beans (246 g; 575kcal, 20 g Protein, 121 g Carbohydrate, 0.7 g Fat, 1.78 g Fat)

干预措施: Rice and Beans (Other)

Isolated Nutrients (ISO)

Active Comparator

This condition is isonitrogenous and a similar nutrient profile to the experimental complementary mixed meal. The drink is comprised of crystalline amino acids, carbohydrate, fat, and fiber that is matched to rice and beans meal composition.

干预措施: Resistance Exercise (Behavioral)

Isolated Nutrients (ISO)

Active Comparator

This condition is isonitrogenous and a similar nutrient profile to the experimental complementary mixed meal. The drink is comprised of crystalline amino acids, carbohydrate, fat, and fiber that is matched to rice and beans meal composition.

干预措施: Isolated Mixture (Dietary Supplement)

结局指标

主要结局

Myofibrillar protein fractional synthesis rate

时间窗: Basal FSR (from -150 to - 30 min), Postprandial FSR (from -30 to 300min)

Myofibrillar protein synthesis rates will be assessed during the postabsorptive and postprandial periods of experimental primed-constant stable isotope infusions.

Plasma Amino Acid Concentrations

时间窗: Post absorptive (-210, -150, -90, -30, 0 min); Post prandial (30, 60, 90, 120, 180, 240, 300 min)

Amino acid concentrations will be assessed in the postabsorptive state (-210, -150, -90, -30, 0 min) and postprandial state (30, 60, 90, 120, 180, 240, 300 min) via LC/MS/MS.

次要结局

  • Activation of Anabolic Signaling Targets(-150 min, -30 min, 300 min)

研究者

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

Nicholas Burd

Associate Professor

University of Illinois at Urbana-Champaign

研究点 (1)

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