Gyires Klára, Zádori Zoltán S, Török Tamás, Mátyus Péter
Department of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Neurochem Int. 2009 Dec;55(7):447-53. doi: 10.1016/j.neuint.2009.05.014. Epub 2009 May 27.
alpha(2)-Adrenoceptors are involved in various physiological functions, particularly in the cardiovascular system and the central nervous system. Different adrenoceptor subtypes (alpha(2A), alpha(2B) and alpha(2C)) have been recognised and the different subtypes may have role in activation of distinct physiological and pharmacological pathways. Some of the actions of alpha(2)-adrenoceptor stimulants are likely to be mediated exclusively by alpha(2A)-adrenoceptor subtype, like antihypertensive and bradycardic effects. alpha(2A)-Adrenoceptor may have dominant role in sedative and hypothermic actions, in inhibition of gastric acid secretion and gastric motor activity, as well as in stabilisation of thrombus. Besides alpha(2A)-adrenergic receptors alpha(2B) and alpha(2C)-adrenoceptor subtypes may also be involved in some of the classical effects of alpha(2)-adrenoceptor stimulants, like in presynaptic regulation of transmitter release and antinociceptive action. alpha(2B)-Adrenoceptor has dominant role in the vasoconstrictor effect of alpha(2)-adrenoceptor agonists, and its activation induces contraction of rat uterus in late pregnancy. alpha(2B)-Adrenoceptor mediates gastric mucosal protective action initiated centrally in the rat, as well as it may have role also in developmental or reproductive processes. alpha(2C)-Adrenoceptor subtypes may be involved in stress-dependent depression and other psychiatric illnesses like attention deficit hyperactivity disorder-together with alpha(2A)-adrenoceptor. alpha(2C)-Adrenergic receptors seem to mediate peripheral actions as well, like venous vasoconstriction. Identification of separate physiological roles for different alpha(2)-adrenergic receptor subtypes could improve design of novel compounds for specific therapeutic goals.
α₂肾上腺素能受体参与多种生理功能,尤其是在心血管系统和中枢神经系统中。已识别出不同的肾上腺素能受体亚型(α₂A、α₂B和α₂C),不同亚型可能在激活不同的生理和药理途径中发挥作用。α₂肾上腺素能受体激动剂的一些作用可能仅由α₂A肾上腺素能受体亚型介导,如降压和心动过缓作用。α₂A肾上腺素能受体可能在镇静、体温降低作用、抑制胃酸分泌和胃运动活性以及血栓稳定中起主导作用。除α₂A肾上腺素能受体外,α₂B和α₂C肾上腺素能受体亚型也可能参与α₂肾上腺素能受体激动剂的一些经典作用,如在突触前调节递质释放和抗伤害感受作用中。α₂B肾上腺素能受体在α₂肾上腺素能受体激动剂的血管收缩作用中起主导作用,其激活可诱导妊娠晚期大鼠子宫收缩。α₂B肾上腺素能受体介导大鼠中枢引发的胃黏膜保护作用,并且它可能在发育或生殖过程中也起作用。α₂C肾上腺素能受体亚型可能与α₂A肾上腺素能受体一起参与应激依赖性抑郁和其他精神疾病,如注意力缺陷多动障碍。α₂C肾上腺素能受体似乎也介导外周作用,如静脉血管收缩。确定不同α₂肾上腺素能受体亚型的单独生理作用可改善针对特定治疗目标的新型化合物的设计。