Effect of Acute Fish Protein Hydrolysates Ingestion on Vascular Function of the Type 2 Diabetes Subjects
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 22
- 试验地点
- 1
- 主要终点
- High performance liquid chromatography
研究概览
简要总结
Type 2 diabetes mellitus (T2DM) is a chronic metabolic disease of abnormal carbohydrate metabolism which is related with high morbidity and mortality rates caused by its complications. One of the major diabetes-related arterial phenotypes thought to be responsible for development of cardiovascular disease is endothelial dysfunction. Nitric oxide (NO) is a potent molecule derived of endothelium, which plays key role in control of vascular tone. In T2DM present endothelial dysfunction due to reduced NO bioavailability. Fish protein hydrolysates (FPH) have been showed to present antioxidant peptides (and high value of ACE inhibition activity. Therefore, the present study aimed to examine whether single dose of FPH ingestion would reversal macro- and microvascular endothelial dysfunction in T2DM.
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
- Double (Participant, Investigator)
盲法说明
Double blind
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
- •Type 2 diabetes mellitus
排除标准
- •History of symptomatic coronary artery disease;
- •Stroke or other known atherosclerotic disease;
- •HIV positive;
- •Alcohol or drug abuse within the past 6 months previous the visit 1;
- •use any antioxidant supplementation
研究组 & 干预措施
Health control
Health young subjects free of diabetes mellitus and nutritional intervention
DM Placebo
Sucralose
干预措施: Placebo (Other)
DM FHP
Fish protein hydrolysates
干预措施: Fish protein hydrolysates (Other)
结局指标
主要结局
High performance liquid chromatography
时间窗: 75 min after nutritional intervention
serum amino acids
Flow-mediated dilation
时间窗: 60 min after nutritional intervention
macrovascular endothelial function
Near infrared spectroscopy
时间窗: 70 min after nutritional intervention
microvascular endothelial function
次要结局
未报告次要终点
研究者
Thiago Alvares
D.sc
Universidade Federal do Rio de Janeiro
