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临床试验/NCT03906409
NCT03906409已完成不适用

Effect of Nutrient Delivery Pattern on Biological Rhythms in Human Skeletal Muscle

University of Bath1 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2019年2月28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
18
试验地点
1
主要终点
Autophagy

研究概览

简要总结

Recent work has established biological rhythms in human skeletal muscle. It remains unknown how the timing and pattern of meals influences these rhythms. Therefore, this study sets out to establish how frequent (CONSTANT) vs infrequent (BOLUS) feeding patterns influence established biological rhythms in skeletal muscle.

详细描述

Human metabolism is regulated on a daily basis via a circadian timing system that coordinates metabolic responses between various tissues. Skeletal muscle is a major site for the oxidation or storage of key metabolites, with recent studies at Bath and Surrey demonstrating biological rhythms in this tissue over a 24-h cycle. It is well established that dysregulated metabolism in skeletal muscle contributes to poor metabolic health and that poor diet is a causal factor in this deterioration. Diet can be characterised by three nutritional considerations: how much is eaten (i.e. quantity/dose), what is eaten (i.e. type) and when it is eaten (i.e. timing). Whilst most dietary approaches and most scientific studies have focused on the first two factors, there is convincing evidence that human health is also dictated by the pattern of nutrient delivery; this includes the frequency and regularity of daily eating occasions, along with their timing both in absolute terms (i.e. time-of-day) and relative to when other inter-related daily events occur - or usually occur (e.g. light exposure, sleep, exercise, etc.).

It remains unknown whether the interaction of such factors may affect the biological rhythms previously documented in human skeletal muscle. In particular, from a basic science perspective, the fundamental contrast between frequent versus infrequent feeding warrants investigation. To this end, 16-24 healthy adults will be randomly allocated to receive their individual daily energy requirements delivered via naso-gastric infusion either continuously over 24 hours (n=8-12; CONSTANT) or as two bolus infusions at the start (0800 h) and mid-point (2000 h) of the monitoring period (n=8-12; BOLUS). Serial skeletal muscle (vastus lateralis) biopsies will be sampled every 4 hours over a controlled 24-h sleep-wake cycle.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Body mass index >19 but <30 kg/m2
  • •Be able and willing to give informed oral and written consent, complete and meet the defined criteria of pre-study questionnaires and screens,
  • •Have a regular sleep cycle with a sleep duration between 6 and 8 hours, do not exhibit extreme morning or evening preference (Horne and Ostberg, 1976)
  • •Agree to keep a constant sleep/wake cycle with a self-selected 8 hour sleep duration (from which it cannot be deviated by more than 30 minutes) for one week prior to the lab study,
  • •Obtain 15 minutes of sunlight within 1.5 hours of waking up and agree to nap only within a 4 h designated nap window for one week prior to the lab study,
  • •Allow confirmation of compliance to these instructions by wearing ActiHeart monitors continuously and complete daily sleep and event diaries for one week before the study session,
  • •Agree to refrain from alcohol, caffeine, heavy exercise and certain food components TWO days before the study session,
  • •Agree to weigh and record daily meals (based on individual energy requirements) for TWO days prior to the study,
  • •Agree to refrain from prescribed and 'over the counter' medication and food/vitamin supplements for a wash-out period three weeks before and during the study.

排除标准

  • •Are taking regular medication (also non-prescribed) or food supplements (e.g vitamins, minerals, fish oil, antioxidant tablets) from which it is not possible to refrain, known to influence: Sleep/alertness/the circadian timing system (e.g beta-blockers, barbituates, antidepressants, benzodiazepines, melatonin, ritalin, modafinil, soporifics, St John's Wort), any of the metabolic functions (e.g. affecting thyroid, kidney, liver or gastrointestinal function)
  • •Any of the inflammatory markers (e.g. aspirin, ibuprofen, antiobiotics, hay fever medication, medication for sore throats and colds)
  • •And/or any of the endothelial markers (e.g. ACE inhibitors and angiotensin (receptor) blockers, diuretics, Beta-blockers, anti-thrombosis medication),
  • •Have a history of any circadian or sleep disorder or metabolic, cardiovascular or chronic infectious / inflammatory disease as confirmed by the GP or the pre-study questionnaires (e.g. a Pittsburgh Sleep Quality Index > 5 will result in exclusion),
  • •Have a history of psychiatric or neurological disease or drug and alcohol abuse,
  • •Have donated over 400 ml of blood in the three months preceding the study,
  • •Have participated in shift work or have travelled across more than two time zones within three weeks of the study,
  • •Do not keep a regular sleep-wake cycle,
  • •Do not refrain from alcohol, caffeine containing drinks (e.g. coffee, coke, tea, redbull), heavy exercise and certain foods (e.g. those high in fat and green vegetables) TWO days before and during the laboratory session,
  • •Normally consume more than 4 cups of caffeinated beverages (e.g. tea, coffee, cola) daily

研究组 & 干预措施

Constant

Active Comparator

Participants will be provided with their daily energy requirements in a continuous drip across the day (1 ml/minute).

干预措施: Constant (Other)

Bolus

Experimental

Participants will be provided with their daily energy requirements in two bolus feeds. One at 08:00-08:15 and one at 20:00-20:15

干预措施: Bolus (Other)

结局指标

主要结局

Autophagy

时间窗: 4 hours

Rhythms in autophagy with different feeding patterns

Transcriptomic, rhythms in human skeletal muscle

时间窗: Over a 24-hour period at a 4 hour resolution

Assessing rhythms in core-clock genes within the muscle samples

次要结局

  • Continuously monitored subcutaneous interstitial glucose concentrations(48-hours)
  • Endocrine responses of systemic blood plasma over 24-hours(24-hours)

研究者

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

James Betts

Professor James Betts

University of Bath

研究点 (1)

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