In Vitro Activation of Human Adrenergic Receptors and Trace Amine-Associated Receptor 1 by Phenethylamine Analogues Present in Food Supplements.
Nicole E T PinckaersW Matthijs BlankesteijnAnastasiya MirchevaXiao ShiAntoon OpperhuizenFrederik-Jan van SchootenMisha F VrolijkPublished in: Nutrients (2024)
Pre-workout supplements are popular among sport athletes and overweight individuals. Phenethylamines (PEAs) and alkylamines (AA) are widely present in these supplements. Although the health effects of these analogues are not well understood yet, they are hypothesised to be agonists of adrenergic (ADR) and trace amine-associated receptors (TAARs). Therefore, we aimed to pharmacologically characterise these compounds by investigating their activating properties of ADRs and TAAR1 in vitro . The potency and efficacy of the selected PEAs and AAs was studied by using cell lines overexpressing human ADRα 1A /α 1B /α 1D /α 2a /α 2B /β 1 /β 2 or TAAR1. Concentration-response relationships are expressed as percentages of the maximal signal obtained by the full ADR agonist adrenaline or the full TAAR1 agonist phenethylamine. Multiple PEAs activated ADRs (EC 50 = 34 nM-690 µM; E max = 8-105%). Almost all PEAs activated TAAR1 (EC 50 = 1.8-92 µM; E max = 40-104%). Our results reveal the pharmacological profile of PEAs and AAs that are often used in food supplements. Several PEAs have strong agonistic properties on multiple receptors and resemble potencies of the endogenous ligands, indicating that they might further stimulate the already activated sympathetic nervous system in exercising athletes via multiple mechanisms. The use of supplements containing one, or a combination of, PEA(s) may pose a health risk for their consumers.
Keyphrases
- health risk
- endothelial cells
- heavy metals
- adverse drug
- healthcare
- induced pluripotent stem cells
- molecular docking
- public health
- human health
- photodynamic therapy
- pluripotent stem cells
- signaling pathway
- risk assessment
- physical activity
- weight loss
- emergency department
- gene expression
- genome wide
- body composition
- body mass index
- dna methylation
- binding protein
- structure activity relationship
- electronic health record
- drug induced
- anterior cruciate ligament