1. Academic Validation
  2. Absorption, Pharmacokinetics, and Urinary Excretion of Pyridines After Consumption of Coffee and Cocoa-Based Products Containing Coffee in a Repeated Dose, Crossover Human Intervention Study

Absorption, Pharmacokinetics, and Urinary Excretion of Pyridines After Consumption of Coffee and Cocoa-Based Products Containing Coffee in a Repeated Dose, Crossover Human Intervention Study

  • Mol Nutr Food Res. 2020 Sep;64(18):e2000489. doi: 10.1002/mnfr.202000489.
Letizia Bresciani 1 Michele Tassotti 1 Alice Rosi 2 Daniela Martini 1 3 Monica Antonini 4 Alessandra Dei Cas 4 Riccardo Bonadonna 4 Furio Brighenti 2 Daniele Del Rio 1 Pedro Mena 2
Affiliations

Affiliations

  • 1 Human Nutrition Unit, Department of Veterinary Science, University of Parma, Via Volturno 39, Parma, 43125, Italy.
  • 2 Human Nutrition Unit, Department of Food and Drug, University of Parma, Via Volturno 39, Parma, 43125, Italy.
  • 3 Department of Food, Environmental and Nutritional Sciences, Università degli Studi di Milano, Via Celoria 2, Milan, 20122, Italy.
  • 4 Division of Endocrinology and Metabolic Diseases, Department of Medicine and Surgery, University of Parma, Via Gramsci 14, Parma, 43126, Italy.
Abstract

Scope: The present study assesses the absorption, pharmacokinetics, and urinary excretion of coffee pyridines and their metabolites after daily regular exposure to specific dosages of coffee or cocoa-based products containing coffee (CBPCC), considering different patterns of consumption.

Methods and results: In a three-arm, crossover, randomized trial, 21 volunteers are requested to randomly consume for 1 month: one cup of espresso coffee per day, three cups of espresso coffee per day, or one cup of espresso coffee plus two CBPCC twice per day. The last day of the one-month treatment, blood and urine samples are collected for 24 h. Trigonelline, N-methylpyridinium, N-methylnicotinamide, and N-methyl-4-pyridone-5-carboxamide are quantified. Trigonelline and N-methylpyridinium absorption curves and 24-h urinary excretion reflect the daily consumption of different servings of coffee or CBPCC, showing also significant differences in main pharmacokinetic parameters. Moreover, inter-subject variability due to sex and smoking is assessed, showing sex-related differences in the metabolism of trigonelline and smoking-related ones for N-methylpyridinium.

Conclusion: The daily exposure to coffee pyridines after consumption of different coffee dosages in a real-life setting is established. This data will be useful for future studies aiming at evaluating the bioactivity of coffee-derived circulating metabolites in cell experiments, mimicking more realistic experimental conditions.

Keywords

bioavailability; coffee; dietary pattern; human intervention study; pyridine.

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