The endocannabinoids (ECs) and N-acylethanolamines (NAEs) are a group of endogenous lipid mediators which have a pleiotropic activity in the body modulating several biological pathways such as: appetite cues, food intake, blood pressure, inflammation, glycaemia, cognition and immunity. The ECs consist of N-arachidonoylethanolamide (AEA) and 2-arachidonoylglycerol (2-AG). They may have agonist activity on cannabinoid receptors CB1 and CB2 which are located in the central nervous system (CNS) and in peripheral tissues such as in the enteric nervous system (ENS), in the liver and in the adipose tissue. NAEs are known as "endocannabinoid-like" molecules and include oleoylethanolamine (OEA), linoleylethanolamine (LEA), and palmitoyletahanolamine (PEA). Evidence indicates that diet composition may affect fasting and post-prandial plasma ECs, N-acylphosphatidylethanolamines (NAPEs) and NAEs profile due to the content of their precursors, fatty acids and amines. It is hypothesized that the concentration of NAPEs, NAEs and ECs in a meal could influence the intestinal concentrations of these lipid mediators that could bind the receptors located on the intestinal mucosa and in turn, differently modulate appetite and energy metabolism. The study is an acute randomized crossover feeding study in ileostmists (n=14), having a breakfast meal low or high in NAPEs, NAEs and ECs. The meals are designed on a database published by our collaborators (University of Naples) and detailed in the research proposal. Concentrations of NAEs and ECs in urine, plasma and ileal fluid, beside the blood glucose, hormonal response, appetite feelings and food intake will be monitored over the experimental days.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Enrollment
14
Milk (150 mL), white bread (46 g), jam (10 g), cocoa powder (15 g), whole-grain cereals (30 g).
Milk (150 mL), whole-grain bread (80 g), jam (10 g), butter (5 g), instant coffee (2 g), dried apples (30 g).
Human Intervention Studies Unit, Ulster University
Coleraine, Co.Londonderry, United Kingdom
RECRUITINGN-acylphosphatidylethanolamines (NAPEs) levels in biofluids
Significant changes from baseline in plasma, urines and, Ileal fluids levels of NAPEs by HPLC-MS analysis.
Time frame: Change from baseline at 2, 4, 6 and, 8 hours after breakfast intake
N-acylethanolamines (NAEs) levels in biofluids
Significant changes from baseline in plasma, urines and, Ileal fluids levels of NAEs by HPLC-MS analysis.
Time frame: Change from baseline at 2, 4, 6 and, 8 hours after breakfast intake
Endocannabinoids levels in biofluids
Significant changes from baseline in plasma, urines and, Ileal fluids levels of ECs by HPLC-MS analysis.
Time frame: Change from baseline at 2, 4, 6 and, 8 hours after breakfast intake
Glycaemia
Measure of glycaemia by using a bedside glucometer.
Time frame: Change from baseline at 2, 4, 6 and, 8 hours after breakfast intake
Appetite sensations
Significant changes from baseline in hunger, satiety, fullness and prospective of consumption.
Time frame: Change from baseline at 2, 4, 6 and, 8 hours after breakfast intake
Glucagon-like peptide 1 (GLP-1) plasmatic levels
Measure of GLP-1 by using of Luminex kits in plasma samples pre-treated with protease inhibitor cocktail.
Time frame: Change from baseline at 2, 4, 6 and, 8 hours after breakfast intake
Glucose-dependent insulinotropic peptide (GIP) plasmatic levels
Measure of GIP by mean of Luminex kits in plasma samples pre-treated with protease inhibitor cocktail.
Time frame: Change from baseline at 2, 4, 6 and, 8 hours after breakfast intake
Insulin plasmatic levels
Measure of insulin by mean of Luminex kits in plasma samples pre-treated with protease inhibitor cocktail.
Time frame: Change from baseline at 2, 4, 6 and, 8 hours after breakfast intake
Glucagon plasmatic levels.
Measure of glucagon by mean of Luminex kits in plasma samples pre-treated with protease inhibitor cocktail.
Time frame: Change from baseline at 2, 4, 6 and, 8 hours after breakfast intake
C-peptide plasmatic levels.
Measure of c-peptide by mean of Luminex kits in plasma samples pre-treated with protease inhibitor cocktail.
Time frame: Change from baseline at 2, 4, 6 and, 8 hours after breakfast intake
Ghrelin plasmatic levels.
Measure of ghrelin by mean of Luminex kits in plasma samples pre-treated with protease inhibitor cocktail.
Time frame: Change from baseline at 2, 4, 6 and, 8 hours after breakfast intake
Leptin plasmatic levels
Measure of leptin by mean of Luminex kits in plasma samples pre-treated with protease inhibitor cocktail.
Time frame: Change from baseline at 2, 4, 6 and, 8 hours after breakfast intake
Energy intake during a buffet meal test
Kilojoules
Time frame: 0 hours
Gut microbiota composition
Microbiota composition will be determined by high throughput sequencing of the 16S ribosomal ribonucleic acid (rRNA) gene. The massive number of sequences obtained will be analyzed by using state of the art bioinformatics tools and the presence and relative abundance of the microbial species occurring in each sample will be determined.
Time frame: Change from baseline at 2, 4, 6 and, 8 hours after breakfast intake
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.