Shearman M S, Strange P G
Department of Biochemistry, Medical School, Queen's Medical Centre, Nottingham, U.K.
Biochem Pharmacol. 1988 Aug 15;37(16):3097-102. doi: 10.1016/0006-2952(88)90306-1.
Specific [3H]ketanserin binding to serotonin 5-HT2 receptors of rat frontal cortex tissue is of high affinity, saturable and unaffected by guanine nucleotides. Antagonists displace [3H]ketanserin from a single recognition site (pseudo-Hill coefficients close to unity), which is also unaffected by guanine nucleotides. Agonist displacement of either [3H]ketanserin or [3H]spiperone from three different membrane preparations showed pseudo-Hill coefficients less than one, and may be described in terms of two agonist binding sites with differing agonist affinities. In the presence of guanine nucleotides, overall agonist affinity was lowered slightly, with little or no change in pseudo-Hill coefficient.
特异性[³H]酮色林与大鼠额叶皮质组织中5-羟色胺5-HT₂受体的结合具有高亲和力、可饱和性且不受鸟嘌呤核苷酸影响。拮抗剂从单一识别位点取代[³H]酮色林(伪希尔系数接近1),该位点也不受鸟嘌呤核苷酸影响。[³H]酮色林或[³H]螺哌隆从三种不同膜制剂中的激动剂取代显示伪希尔系数小于1,并且可以用具有不同激动剂亲和力的两个激动剂结合位点来描述。在鸟嘌呤核苷酸存在的情况下,总体激动剂亲和力略有降低,伪希尔系数几乎没有变化或没有变化。