Dehlin E, Marcusson J, Fowler C J, Winblad B
J Neural Transm. 1982;54(1-2):91-103. doi: 10.1007/BF01249282.
The binding of [3H]-5-hydroxytryptamine ([3H]-5-HT) to homogenates of human brain has been studied. The specific binding is saturable, with a Kd (frontal cortex) of 12 /+- 2 nM, and is inhibited by non-radioactive 5-HT (IC50=26 nM) and D-Lysergic acid diethylamide (IC50=20 nM). Specific, but not non-specific binding of [3H]-5-TH was inhibited by incubation of the homogenates at 50 degrees C. The binding of [3H]-5-HT across the human brain was not uniform, the highest binding being found in the substantia nigra and hippocampus, and the lowest in the thalamus and pons. The Kd of the binding sites towards 5-HT did, however, appear to be similar for the different brain regions.
对[3H]-5-羟色胺([3H]-5-HT)与人脑匀浆的结合进行了研究。特异性结合具有饱和性,额叶皮质的解离常数(Kd)为12±2 nM,且受到非放射性5-HT(半数抑制浓度[IC50]=26 nM)和麦角酸二乙胺(IC50=20 nM)的抑制。将匀浆在50℃孵育可抑制[3H]-5-TH的特异性结合,但不抑制非特异性结合。[3H]-5-HT在人脑中的结合并不均匀,在黑质和海马中结合最高,而在丘脑和脑桥中最低。然而,不同脑区的5-HT结合位点的Kd似乎相似。