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食品补充剂中苯乙胺类似物对人肾上腺素能受体和痕量胺相关受体 1 的激活作用。

Activation of Human Adrenergic Receptors and Trace Amine-Associated Receptor 1 by Phenethylamine Analogues Present in Food Supplements.

机构信息

Department of Pharmacology and Toxicology, Maastricht University, 6200 MD Maastricht, The Netherlands.

Research Institute of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University, 6200 MD Maastricht, The Netherlands.

出版信息

Nutrients. 2024 May 22;16(11):1567. doi: 10.3390/nu16111567.

Abstract

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 . The potency and efficacy of the selected PEAs and AAs was studied by using cell lines overexpressing human ADRα/α/α/α/α/β/β 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 = 34 nM-690 µM; E = 8-105%). Almost all PEAs activated TAAR1 (EC = 1.8-92 µM; E = 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.

摘要

健身前补充剂在运动员和超重人群中很受欢迎。苯乙胺(PEAs)和烷基胺(AA)广泛存在于这些补充剂中。虽然这些类似物的健康影响尚未得到充分理解,但据推测它们是儿茶酚胺(ADR)和微量胺相关受体(TAARs)的激动剂。因此,我们旨在通过研究它们对 ADR 和 TAAR1 的激活特性来对这些化合物进行药理学表征。通过使用过表达人 ADRα/α/α/α/α/β/β或 TAAR1 的细胞系,研究了选定的 PEAs 和 AAs 的效力和效能。浓度-反应关系表示为通过全 ADR 激动剂肾上腺素或全 TAAR1 激动剂苯乙胺获得的最大信号的百分比。多种 PEAs 激活了 ADR(EC = 34 nM-690 µM;E = 8-105%)。几乎所有的 PEAs 都激活了 TAAR1(EC = 1.8-92 µM;E = 40-104%)。我们的结果揭示了经常在食品补充剂中使用的 PEAs 和 AAs 的药理学特征。几种 PEAs 对多种受体具有强烈的激动作用,类似于内源性配体的效力,表明它们可能通过多种机制进一步刺激运动中已经激活的交感神经系统。含有一种或多种 PEA 的补充剂的使用可能会对消费者的健康构成风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/038b/11174489/9ebfad0efbcd/nutrients-16-01567-g0A1.jpg

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