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Идёт набор NCT05233722

mTOR as Mediator of Insulin Sensitivity Study

Без фазы С лечением Insulin Sensitivity

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Exercise, Insulin infusion, Placebo, Rapamycin.
Кому может быть актуально
Состояния в реестре: Insulin Sensitivity. Базовые параметры: 22 лет — 35 лет · Мужчины.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Дания
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Mechanistic Target of Rapamycin (mTOR) as Mediator of Exercise-induced Insulin Sensitivity Study

Обзор

The study investigates the role of mTOR in mediating enhancement of muscle insulin sensitivity following a single bout of exercise. This will be investigated in young healthy male subjects by administering the pharmacological mTOR inhibitor Rapamycin in a crossover blinded experimental setup known to enhance muscle insulin sensitivity following one-legged knee-extensor exercise.

Подробное описание

Trial A: During trial A the study subject will arrive at the research laboratory and eat a morning meal at 6:30 a.m. corresponding to 5% of the daily energy requirements. It is requested that the study subject will arrive in a car or with public transportation. At the same time, the subject will ingest 16 mg of Rapamycin or placebo (800 mg Calcium) in pill form. Following ingestion, the study subject will rest for 2 hour and at that time catheters are inserted in both femoral veins, the femoral artery in one of the legs and in each forearm vein (antecubital veins) for later blood sampling and intravenous infusion of insulin, glucose, stable D2-glucose and stable 13C6-phenylalanine. At 8:30 a.m. the study subjects will perform one-leg knee extension exercise for 1 hour at an intensity of 80% of maximal work capacity. In this work protocol there are inserted 3 intervals of 5 minutes duration where the study subject works at 100% of maximal intensity with the purpose of securing a full activation/recruiting of all muscle fibers. Immediately following conclusion of the exercise bout 13C6-phenylalanine is infused for later determination of muscle protein synthesis. 2 hours into the recovery from exercise D2-glucose is infused for later determination of hepatic glucose production. 4 hours into the recovery from exercise an euglycaemic hyperinsulinemic clamp will be initiated for 2 hours for determination of insulin stimulated muscle glucose uptake. Muscle biopsies from the m. vastus lateralis muscle in one or both legs will be taken before, immediately after, as well as 2, 4 and 6 hours after conclusion of exercise. Pulmonary oxygen uptake is measured with the use of an online system before, during and after exercise and is used for determination of substrate metabolism. Blood samples from the femoral veins in both legs and the femoral artery in one of the legs are drawn before, during exercise, and during the recovery period after exercise. At the same time blood flow is measured in the femoral arteries in both legs with the use of Doppler technique. Determination of arteriovenous difference (AV difference) by simultaneous measurement of blood flow enables us to calculate skeletal muscle glucose uptake and uptake/release of relevant substances (proteins, peptides and metabolites etc.). The experimental part of trial A is completed at 15:30 p.m. The study subject will be given food and drink and will be observed for one hour before they may leave the research laboratory.

Trial B is an identical protocol, except that the subject will receive opposite drug from trial A (Rapamycin or placebo). Trial A and B will be separated by a minimum of 14 days.

Вмешательства

  • Другое Exercise
    1 hour of one-legged knee-extensor exercise followed by 4 hours of rest
  • Процедура Insulin infusion
    2 hours of Euglycemic Hyperinsulinemic Clamp
  • Препарат Placebo
    Administration of 800 mg of calcium tablets
  • Препарат Rapamycin
    Administration of 16 mg of Rapamycin tablets

Первичные конечные точки

  • Insulin stimulated muscle glucose uptake [Срок оценки: Through study completion, approx. 1 year.]
Вторичные конечные точки (2)
  • Insulin stimulated muscle protein synthesis [Срок оценки: 1-2 year.]
  • Posttranslational modification of proteins in muscle biopsies [Срок оценки: 5 years]

Критерии участия

Критерии включения

  • Healthy persons (no known disease) without diabetes in the family
  • No use of medications
  • Non-smokers
  • Men
  • Age 22-35 years
  • Physical activity level (VO2peak) between 30-50 mL O2/min/kg
  • BMI between 18.0 and 25.0

Критерии исключения

  • Women
  • Physical activity (e.g., running, cycling, fitness, etc.) above 6 hours a week.
  • Persons who show signs of metabolic diseases, hematologic diseases, reduced liver function, human immunodeficiency virus (HIV), hepatitis, thyroid diseases or other signs of disease that may affect the outcome of the study or the study subject's wellbeing will be excluded.
  • Acute sickness less than 2 weeks prior to study start.
  • If disease appears or is identified and/or a need for medication arises after inclusion but before initiation of the study.

Disease during conclusion of the study

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Нерандомизированное
Модель
Перекрёстный дизайн
Маскирование
Двойное слепое
Основная цель
Фундаментальное исследование

Центры проведения

Дания · 1 центр
  • University of Copenhagen — Copenhagen

Идентификаторы

NCT: NCT05233722 · Rapa Study

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗