Rommelspacher H, Strauss S, Fähndrich E, Haug H J
J Neural Transm. 1987;69(1-2):85-96. doi: 10.1007/BF01244099.
[3H] UK-14,304 was used to investigate alpha 2-adrenoceptors in rat brain and human platelets. Receptor pharmacology revealed that the ligand binds with high affinity to alpha 2-adrenoceptors. Psychoactive substances like neuroleptics, antidepressants, and beta-carbolines displace [3H] UK-14,304 from its binding sites in the lower micromolar range. A Hill number around 2 for most neuroleptics suggests a positive cooperativity with the alpha 2-adrenoceptors. Comparative studies with [3H] UK-14,304 and [3H] clonidine utilizing platelet membranes from human volunteers demonstrated that the former ligand is more suitable to investigate possible changes of alpha 2-adrenoceptors; [3H] UK-14,304 labels more receptors with a lower standard deviation, whereby the volume of the blood sample amounted to 35 ml instead of 50 ml required for [3H] clonidine as ligand. No sex differences of binding constants were detected, however an inverse correlation of maximum number of binding sites and affinity was found for female subjects with both ligands. No age-dependent changes of Bmax and KD-values were observed in the range of 24 to 59 years.
[3H] UK - 14,304被用于研究大鼠脑和人血小板中的α2 - 肾上腺素能受体。受体药理学研究表明,该配体与α2 - 肾上腺素能受体具有高亲和力。精神活性物质如抗精神病药、抗抑郁药和β - 咔啉在低微摩尔浓度范围内可将[3H] UK - 14,304从其结合位点上置换下来。大多数抗精神病药的希尔系数约为2,表明与α2 - 肾上腺素能受体存在正协同性。利用人类志愿者的血小板膜对[3H] UK - 14,304和[3H]可乐定进行的比较研究表明,前一种配体更适合研究α2 - 肾上腺素能受体的可能变化;[3H] UK - 14,304标记的受体更多,标准差更低,而作为配体的[3H]可乐定所需的血样体积为50 ml,[3H] UK - 14,304所需血样体积为35 ml。未检测到结合常数的性别差异,然而,对于两种配体而言,女性受试者的最大结合位点数与亲和力呈负相关。在24至59岁范围内未观察到Bmax和KD值随年龄的变化。