Pole of Pharmacology and Therapeutics (FATH), Institut de Recherche Experimentale et Clinique (IREC), Université Catholique de Louvain, B1.57.04, 57 Avenue Hippocrate, 1200 Brussels, Belgium.
Department of Medicine, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, 10 Avenue Hippocrate, 1200 Brussels, Belgium.
Cells. 2020 Dec 2;9(12):2584. doi: 10.3390/cells9122584.
The third isotype of beta-adrenoreceptors (β3-AR) has recently come (back) into focus after the observation of its expression in white and beige human adipocytes and its implication in metabolic regulation. This coincides with the recent development and marketing of agonists at the human receptor with superior specificity. Twenty years ago, however, we and others described the expression of β3-AR in human myocardium and its regulation of contractility and cardiac remodeling. Subsequent work from many laboratories has since expanded the characterization of β3-AR involvement in many aspects of cardiovascular physio(patho)logy, justifying the present effort to update current paradigms under the light of the most recent evidence.
β 肾上腺素能受体的第三种亚型(β3-AR)最近重新成为研究焦点,这是因为人们观察到它在白色和米色人类脂肪细胞中的表达,并认为它与代谢调节有关。这与最近开发和上市的具有更高特异性的人类受体激动剂不谋而合。然而,20 年前,我们和其他人就已经描述了 β3-AR 在人类心肌中的表达及其对心肌收缩力和心脏重构的调节作用。此后,许多实验室的后续工作扩大了对 β3-AR 参与心血管生理(病理)生理学诸多方面的认识,这也证明了目前根据最新证据更新现有范式的必要性。