Show pageBacklinksCite current pageExport to PDFBack to top This page is read only. You can view the source, but not change it. Ask your administrator if you think this is wrong. The alpha-2 (α2) adrenergic receptor (or adrenoceptor) is a [[G protein coupled receptor]] (GPCR) associated with the Gi heterotrimeric G-protein. It consists of three highly homologous subtypes, including α2A-, α2B-, and α2C-adrenergic. Some species other than humans express a fourth α2D-adrenergic receptor as well. Catecholamines like norepinephrine (noradrenaline) and epinephrine (adrenaline) signal through the α2-adrenergic receptor in the central and peripheral nervous systems. The continued quest for a novel sedating agent for intensive care and need for drugs to blunt the stress response to the surgical stimulus has led to the increasing use of α-2 adrenergic agonists in these clinical settings. These drugs have a favorable pharmacological profile owing to their sympatholytic, sedative, analgesic, anxiolytic, and anesthetic drugs sparing effects. Clonidine, which was introduced earlier as an anti-hypertensive was commonly used α-2 adrenergic agonist in various clinical scenarios including regional and general anesthesia. Newer more selective α-2 agonist [[dexmedetomidine]] alpha_2_adrenergic_receptor.txt Last modified: 2024/06/07 02:49by 127.0.0.1