Platelet Aggregation and Inflammation Clinical Trial
Official title:
Investigation of in Vivo Anti-inflammatory and Anti-platelet Mechanisms of Natural Extract by Modulating PAF Metabolism and Actions
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.
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.
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