跳至主要内容
临床试验/NCT04436263
NCT04436263Unknown不适用

Investigation of in Vivo Anti-inflammatory and Anti-platelet Mechanisms of Natural Extract by Modulating PAF Metabolism and Actions

Harokopio University1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2020年1月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
15
试验地点
1
主要终点
Effect on platelet aggregation

研究概览

简要总结

The purpose of this study is to investigate the anti-platelet and anti-inflammatory properties of a winery by-products extract as well as to detect extract compounds and their metabolites in biological fluids. The study is a randomized, double-blind, crossover, placebo controlled postprandial study in healthy women.

详细描述

The well-known cardioprotective and metabolic effects of wine consumption are mainly attributed to its micro-constituents. Grape pomace (GP) is a by-product of the winemaking process and consists mainly of skins and seeds. Winery by-products are a cheap and rich source of similar-to wine micro-constituents, which can be used either to enrich other foods or to be included in food supplements targeting the prevention or partially the therapy of cardiovascular diseases.In this line, our previous results revealed the potent in vitro anti-platelet effects of a specific ethanol-water extract rich in Platelet-Activating Factor inhibitors from winery by-products.

The purpose of this study is to investigate the in vivo anti-platelet and anti-inflammatory properties of the specific winery by-products extract as well as to detect the extract compounds and their metabolites in biological fluids.

Therefore a randomized double-blind, crossover, placebo controlled postprandial study in healthy women will be implemented. For this purpose, 15 healthy women will participate in the protocol. The two daily trials will take place during specific days based on their menstrual cycle. Three days before each blood collection the volunteers will be instructed to abstain from food and beverages rich in phenolic compounds and their dietary intake will be recorded (three 24h recalls and one food frequency questionnaire). The blood collections will be carried out after 8h fasting. At trial day, the volunteers will bring the first morning urine sample and anthropometric measurements will take place (weight, height, waist/hip circumference, bioelectrical impedance). Then a venous catheter will be placed and after 10 minutes the fasting blood will be collected. Volunteers will proceed to the consumption of a standardized meal (1131 kcal, 19.7% carbohydrates, 11.2% protein, 66.7% fat) along with the capsules (study extract or placebo). The type of the capsules consumed (study extract or placebo) will be randomized and blind during the two intervention days for both volunteers and investigators. Blood will be drown after the meal consumption and for the next 6h (every 30minutes for the first 4h and every 1h for the next 2h). Serum, plasma, platelet-rich plasma, leukocyte-rich plasma and urine samples will be isolated at certain time points during trial days so that the anti-platelet, anti-inflammatory and antioxidant effects of the study extract can be evaluated.

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
Triple (Participant, Care Provider, Investigator)

入排标准

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

入选标准

  • •BMI: 22-32 kg/m2

排除标准

  • •Systematic medication
  • •Chronic disease conditions
  • •Specific dietary conditions (vegeterian, vegan...)
  • •Eating disorders

研究组 & 干预措施

Supplement

Experimental

Ethanol-water extract of winery by-products

干预措施: Supplement (Behavioral)

Placebo

Placebo Comparator

Maltodextrin-based placebo

干预措施: Placebo (Behavioral)

结局指标

主要结局

Effect on platelet aggregation

时间窗: Change between timepoints (before meal consumption, 30min, 90min, 150min, 210min, 300min) of the 6hour trial and between the two different interventions

% Change of EC50 value of platelet aggregation against PAF

Effect on inflammatory markers

时间窗: Change between timepoints (before meal consumption, 0min, 30min, 60min, 90min, 120min, 150min, 180min, 210min, 240min, 300min, 360min) of the 6hour trial and between the two different interventions

Change in PAF degradation enzyme activity (Lp-PLA2)

Effect on inflammatory markers

时间窗: Change between timepoints (before meal consumption, 60min, 120min, 180min, 210min, 240min, 300min, 360min) of the 6hour trial and between the two different interventions

Change in PAF biosynthetic enzymes activity (lyso-PAF AT)

Effect on inflammatory markers

时间窗: Change between timepoints (before meal consumption, 60min, 120min, 180min, 240min, 360min) of the 6hour trial and between the two different interventions

Change in PAF levels Change in PAF degradation enzyme activity (Lp-PLA2) Change in PAF levels IL6

次要结局

  • Effect on classical biochemical markers(Change between timepoints (before meal consumption, 0min, 30min, 60min, 90min, 120min, 150min, 180min, 210min, 240min, 300min, 360min) of the 6hour trial and between the two different interventions)
  • Detection and estimation of extract compounds metabolites(Change between timepoints (before meal consumption, 60min, 120min, 240min, 360min) of the 6hour trial and between the two different interventions)

研究者

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

Elizabeth Fragopoulou

Assistant Professor in Biological Chemistry

Harokopio University

研究点 (1)

Loading locations...

相似试验