Sawutz D G, Krafte D S, Oleynek J J, Ault B
Department of Biochemistry, Sterling Winthrop Pharmaceuticals Research Division, Collegeville, PA 19426, USA.
J Recept Signal Transduct Res. 1995 Jul;15(6):829-46. doi: 10.3109/10799899509049860.
AMPA receptors may play an important role in acute and chronic neurodegenerative diseases. An assay for the specific binding of [3H]-amino-3-hydroxy-5-methylisoxazole-4-propionic acid (AMPA) to receptors in membranes from post-mortem human brain is described, which can be used in screening for selective AMPA receptor antagonists. Membranes were prepared from frozen human adult hippocampus and whole fetal brain tissues. [3H]-AMPA binding to human hippocampus was saturable; Scatchard analysis of equilibrium binding data indicated high and low affinity sites with affinity binding constants (KD) of 3.4 +/- 0.5 nM and 65 +/- 9 nM (n = 7) respectively. Biphasic association and dissociation rate constants for [3H]-AMPA binding were consistent with the biphasic Scatchard analysis. Inhibition of [3H]-AMPA binding revealed a rank order of potency as quisqualate = AMPA > BOAA > L-glutamate = DNQX = CNQX > kainate > L-aspartate = NMDA. AMPA receptors in human fetal brain had a comparable pharmacology. AMPA/kainate receptors were expressed in frog oocytes following injection of RNA prepared from human fetal brain. Human brain tissues may therefore be utilized for screening and functional analysis of AMPA receptor antagonists.
AMPA受体可能在急性和慢性神经退行性疾病中发挥重要作用。本文描述了一种用于检测[3H]-氨基-3-羟基-5-甲基异恶唑-4-丙酸(AMPA)与死后人类大脑膜中受体特异性结合的试验,该试验可用于筛选选择性AMPA受体拮抗剂。膜取自冷冻的成人人类海马体和整个胎儿脑组织。[3H]-AMPA与人海马体的结合具有饱和性;对平衡结合数据进行Scatchard分析表明存在高亲和力和低亲和力位点,其亲和结合常数(KD)分别为3.4±0.5 nM和65±9 nM(n = 7)。[3H]-AMPA结合的双相缔合和解离速率常数与双相Scatchard分析一致。对[3H]-AMPA结合的抑制显示出如下效力顺序:quisqualate = AMPA > BOAA > L-谷氨酸 = DNQX = CNQX > 海人酸 > L-天冬氨酸 = NMDA。人类胎儿大脑中的AMPA受体具有类似的药理学特性。注射从人类胎儿大脑制备的RNA后,AMPA/海人酸受体在蛙卵母细胞中表达。因此,人类脑组织可用于AMPA受体拮抗剂的筛选和功能分析。