The adrenergic receptors are metabolic G protein-coupled receptors. They are the targets of catecholamines. The binding of an agonist to them causes a sympathetic response.
The α-2 adrenergic receptor (A2AR) inhibits insulin or glucagons release.
The β-1 adrenergic receptor (B1AR) increases cardiac output and secretion of rennin and ghrelin.[1]
An activated G protein-coupled receptor (human β-2 adrenergic receptor in blue ) in a complex with a heterotrimeric G protein (3 subunits:reddish to orange-brown) and hormone (gold) (3sn6), resolution 3.2Å. The boundaries of the membrane in which the GPCR sits are represented in light green.
Alprenolol and Propranolol are B2AR antagonists used in treatment of angina pectoris. Timolol ia a B2AR antagonist used in treatment of glaucoma. Carvedilol is A2AR and B2AR antagonist used in treatment of high blood pressure. Salbutamol (Ventolin) and Salmeterol are B2AR agonists used for muscle relaxation in asthma attacks.
↑Strosberg AD. Structure and function of the beta 3-adrenergic receptor. Annu Rev Pharmacol Toxicol. 1997;37:421-50. PMID:9131260 doi:10.1146/annurev.pharmtox.37.1.421
↑Cherezov V, Rosenbaum DM, Hanson MA, Rasmussen SG, Thian FS, Kobilka TS, Choi HJ, Kuhn P, Weis WI, Kobilka BK, Stevens RC. High-resolution crystal structure of an engineered human beta2-adrenergic G protein-coupled receptor. Science. 2007 Nov 23;318(5854):1258-65. Epub 2007 Oct 25. PMID:17962520
Robert J. Lefkowitz and Brian K. Kobilka share the 2012 Nobel Prize in Chemistry for work on GPCRs that includes solving the first structures of a ligand-activated GPCR (2007) and the first activated GPCR in complex with its G protein (2011). A detailed description of the laureates' body of work on this class of receptors with images is here.