Johansson P
Comp Biochem Physiol C Comp Pharmacol Toxicol. 1984;78(2):253-61. doi: 10.1016/0742-8413(84)90079-3.
On anatomical and functional bases, alpha-adrenoceptors have been divided into pre- and postsynaptic alpha-adrenoceptors. Recently, alpha-adrenoceptors have been classified as alpha 1 and alpha 2 according to their pharmacological responses, irrespective of their anatomical location. The presynaptic alpha-adrenoceptors, which have been recognized as alpha 2, determine the frequency of the nerve impulses travelling along the axon and also the amount of transmitter released per nerve impulse from the varicose terminal. Postsynaptic alpha-adrenoceptors have been recognized in various tissues including smooth muscle, pancreatic islets, fat cells, platelets and other tissues. Both alpha 1- and alpha 2-adrenoceptors have been located postsynaptically. alpha-Adrenoceptors have been found also in the central nervous system. Generally, they fall into the same categories (alpha 1 and alpha 2) as the peripheral alpha-adrenoceptors. A new class of drugs, the so called calcium blockers, inhibit the postsynaptic response to alpha 2 stimulation but not the alpha 1-mediated response, indicating that the alpha 2-adrenoceptors are dependent on Ca2+ ions for their function. In the most primitive group of vertebrates, the fishes, alpha-adrenoceptors seem to be different in as much as they do not respond to many of the classical drugs employed to distinguish between alpha-adrenoceptors in mammals. In reptiles and amphibians alpha 2-adrenoceptors have been shown to exist. These receptors are involved in the regulation of melanocytes. In the most advanced non-mammalian vertebrates (birds) both peripheral and central alpha-adrenoceptors seem to be qualitatively similar to the mammalian types.
基于解剖学和功能学基础,α - 肾上腺素能受体已被分为突触前和突触后α - 肾上腺素能受体。最近,α - 肾上腺素能受体根据其药理反应被分类为α1和α2,而不考虑其解剖位置。已被认定为α2的突触前α - 肾上腺素能受体,决定了沿轴突传播的神经冲动频率,以及曲张终末每个神经冲动释放的递质数量。突触后α - 肾上腺素能受体已在包括平滑肌、胰岛、脂肪细胞、血小板和其他组织在内的各种组织中被识别。α1和α2肾上腺素能受体均位于突触后。α - 肾上腺素能受体也已在中枢神经系统中被发现。一般来说,它们与外周α - 肾上腺素能受体属于同一类别(α1和α2)。一类新的药物,即所谓的钙阻滞剂,抑制对α2刺激的突触后反应,但不抑制α1介导的反应,这表明α2 - 肾上腺素能受体的功能依赖于Ca2 +离子。在最原始的脊椎动物类群鱼类中,α - 肾上腺素能受体似乎有所不同,因为它们对许多用于区分哺乳动物α - 肾上腺素能受体的经典药物没有反应。在爬行动物和两栖动物中已证明存在α2 - 肾上腺素能受体。这些受体参与黑素细胞的调节。在最先进的非哺乳动物脊椎动物(鸟类)中,外周和中枢α - 肾上腺素能受体在性质上似乎与哺乳动物类型相似。