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临床试验/NCT02084797
NCT02084797已完成不适用

Revisiting the Human Sweat Gland - Does Arginine Vasopressin Modulate Sweat Sodium Concentration Via the V2 Receptor?

Oakland University1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2011年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
10
试验地点
1
主要终点
Sweat Sodium Concentration Obtained After the Steady-state Portion of the Trial

研究概览

简要总结

This primary aim of this study was to critically assess whether or not sweat water content and sodium concentration were acutely regulated by dynamic changes in antidiuretic hormone (arginine vasopressin or AVP) acting on the Vasopressin 2 receptor (V2R) during exercise. Secondary aims were to evaluate running performance and core temperature to further characterize the role of AVP in the coordinated balance of fluid and temperature homeostasis during exercise. The primary hypothesis was that activation of the V2R in sweat glands would result in water reabsorption and fluid conservation during endurance exercise.

详细描述

Ten healthy habitual runners (> 50km running per week) between 18-60 years of age participated in this double blind randomized control trial. Each subject presented to the exercise lab on four separate occasions. Trial 1 was a familiarization trial to determine each subject's maximal aerobic capacity and peak treadmill running speak (VO2 Peak test). Trials 2, 3 and 4 utilized the same exact protocol, differing only in pharmacological intervention. In a randomized, double-blind order (both participant and investigator blinded to the intervention), either a placebo pill, the V2 receptor antagonist tolvaptan (Samsca™, 30mg tablet), or the V2 receptor agonist desmopressin (DDAVP™, 0.2mg tablet) was ingested along with the CorTemp™ Core Temperature Sensor two hours before commencement of the Exercise Trial with 240mL of bottled water. The exercise protocol consisted of 60 minutes of treadmill running at 60% of peak speed (steady-state) followed by a performance test (the VO2 Peak test). Blood, saliva and urine, were collected before the exercise trial (baseline) and again after both the steady-state run and performance runs. Sweat was obtained from sweat patches after both the steady-state and performance runs. Core temperature, fluid intake, performance time, body weight, thirst and sodium palatability ratings were also assessed. Free access to water was allowed during the trial and all urine produced during the trial was measured and collected. The main outcome measure was sweat sodium concentration.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy (no acute or chronic medical conditions or regular prescription medication use), habitual (>50km/week)
  • Distance runners between the ages of 18-60 years.

排除标准

  • Individuals with chronic medical problems which require regular prescription medication
  • Runners with pre-existing kidney problems
  • Unable to sense thirst
  • Difficulty swallowing
  • Gastrointestinal disorders
  • History of fainting associated with blood draw.

研究组 & 干预措施

all study participants

Experimental

All study participants received all interventions. V2R Antagonist: 30mg Tolvaptan tablet ingested 2 hours before exercise. V2R agonist: 0.2mg DDAVP tablet ingested 2 hours before exercise Placebo

干预措施: V2R (Vasopressin 2 receptor) (Drug)

结局指标

主要结局

Sweat Sodium Concentration Obtained After the Steady-state Portion of the Trial

时间窗: 4 study trials (4 weeks)

Changes in sweat sodium concentration will parallel changes in urine sodium concentration with use of the V2R antagonist, agonist and placebo if the primary hypothesis is true (sweat sodium is regulated by the V2R, similar to how urine sodium is regulated by principle cells located within in the kidney collecting duct)

次要结局

  • Urine Sodium Concentration After the Steady-state Portion of the Trial(4 study trials (4 weeks))
  • Blood Sodium Concentration(4 study trials (4 weeks))
  • Saliva Sodium Concentration(4 trials (4 weeks))

研究者

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

Tamara Hew-Butler

Assoc Prof Exercise Science, Exercise Science

Oakland University

研究点 (1)

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