Autophagy Maintains Vascular Function Through a Novel Glycolysis-linked Pathway Regulating eNOS
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 16
- 试验地点
- 1
- 主要终点
- Change in biomarker Atg7 after chronic exercise training
研究概览
简要总结
Aging is inevitable and is the primary risk factor for developing cardiovascular disease. The molecular mechanisms that drive vascular dysfunction in the context of aging are incompletely understood. The overall hypothesis is that the age-related decline in endothelial cell (EC) autophagy leads to arterial dysfunction. This study will determine whether physiological shear-stress affects autophagosome formation and nitrous oxide (NO) generation in ECs.
详细描述
It is hypothesized that genetic autophagy suppression prevents shear-stress induced purinergic signaling to endothelial nitrous oxide synthase (eNOS) and this pathway will be evaluated in primary arterial ECs obtained from older adult (> 60 years) and adult (18-30 years) subjects before and following rhythmic handgrip exercise that elevates brachial artery shear-rate similarly in both groups. ECs will be used to quantify markers of EC autophagy, eNOS activation, and NO generation. The study will also determine whether exercise-training attenuates the aging-associated decline in EC autophagy, and whether intact autophagy is required for training-induced vascular improvements. To evaluate this potential, it will be determined whether one-limb rhythmic handgrip exercise training by older adult (> 60 y) human subjects is sufficient to elevate basal and shear-induced EC autophagy initiation, eNOS activation, and NO generation vs. the contralateral sedentary limb. Results from this work have tremendous potential to reveal a new therapeutic target and approach for restoring / maintaining vascular function in the aging population.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Single Group
- 主要目的
- Basic Science
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 90 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Candidates must be between 18 and 90 y of age
- •Candidates must be free of overt disease as assessed by a) medical history; b) standard blood chemistries (chem. 7 panel), c) ECG at rest; d) limb vascular examination (ankle-brachial BP index > 0.9); e) resting BP < 140/90 mmHg; and f) skinfold % body fat assessment.
- •Subjects will have a body mass index (BMI) between 19 and 30 and have plasma glucose concentrations < 7.0 mmol/L under fasting conditions and < 11.1 mmol/L at 120 minutes of an oral glucose tolerance test (OGTT)
排除标准
- •Candidates <18 or >90 y of age
- •Candidates demonstrating abnormal ECG, ankle-brachial BP index <0.9, resting BP > 140/90
- •Candidates demonstrating a BMI <19 or > 30
- •Candidates demonstrating plasma glucose concentrations > 7.0 mmol/L under fasting conditions and > 11.1 mmol/L at 120 minutes of an oral glucose tolerance test (OGTT)
- •Candidates demonstrating dyslipidemia (plasma total cholesterol > 240 mg/dl with LDL-cholesterol > 160 mg/dl)
- •Candidates reporting a history of myocardial infarction, unstable cardiac ischemia, recent cardiac catheterization, carotid artery disease, transient ischemic attack
- •Women taking hormone replacement therapy (HRT) currently or in the preceding year will be excluded from the proposed studies due to the direct vascular effects of HRT.
研究组 & 干预措施
Healthy Adult Subjects
Healthy adult subjects (18 - 30 years) will be assessed for markers of EC autophagy, eNOS activation, and NO generation before and after Rhythmic Handgrip Exercise
干预措施: Rhythmic Handgrip Exercise (Other)
Healthy Older Adult Subjects
Healthy older adult subjects (> 60 years) will be assessed for markers of EC autophagy, eNOS activation, and NO generation before and after Rhythmic Handgrip Exercise and after Chronic Exercise Training.
干预措施: Rhythmic Handgrip Exercise (Other)
Healthy Older Adult Subjects
Healthy older adult subjects (> 60 years) will be assessed for markers of EC autophagy, eNOS activation, and NO generation before and after Rhythmic Handgrip Exercise and after Chronic Exercise Training.
干预措施: Chronic Exercise Training (Other)
结局指标
主要结局
Change in biomarker Atg7 after chronic exercise training
时间窗: 8 weeks
Change in biomarker beclin-1 after Rhythmic Handgrip Exercise
时间窗: 60 min
Change in biomarker Atg3 after Rhythmic Handgrip Exercise
时间窗: 60 min
Change in biomarker Atg5 after Rhythmic Handgrip Exercise
时间窗: 60 min
Change in biomarker Atg7 after Rhythmic Handgrip Exercise
时间窗: 60 min
Change in biomarker Lamp1 after Rhythmic Handgrip Exercise
时间窗: 60 min
Change in biomarker Lamp2 after Rhythmic Handgrip Exercise
时间窗: 60 min
Change in biomarker p62 after Rhythmic Handgrip Exercise
时间窗: 60 min
Change in biomarker beclin-1 after chronic exercise training
时间窗: 8 weeks
Change in biomarker Atg3 after chronic exercise training
时间窗: 8 weeks
Change in biomarker Atg5 after chronic exercise training
时间窗: 8 weeks
Change in biomarker Lamp1 after chronic exercise training
时间窗: 8 weeks
Change in biomarker Lamp2 after chronic exercise training
时间窗: 8 weeks
Change in biomarker p62 after chronic exercise training
时间窗: 8 weeks
次要结局
- Change in biomarker p-eNOSS1177 after Rhythmic Handgrip Exercise(60 min)
- Change in radial arterial diameter after chronic exercise training(8 weeks)
- Change in radial arterial flow rate after chronic exercise training(8 weeks)
- Change in radial arterial diameter after Rhythmic Handgrip Exercise(60 min)
- Change in radial arterial flow rate after Rhythmic Handgrip Exercise(60 min)
- Change in biomarker p-eNOSS1177 after chronic exercise training(8 weeks)
研究者
John David Symons
Professor
University of Utah