Carlin R K, Siekevitz P
J Neurochem. 1984 Oct;43(4):1011-7. doi: 10.1111/j.1471-4159.1984.tb12837.x.
The binding of [3H]GABA and [3H]flunitrazepam was performed with synaptic membranes and post-synaptic densities (PSDs) isolated from canine cerebral cortex and cerebellum. Two GABA binding sites were found with cerebral cortex membranes but only one with cerebellar membranes. PSDs isolated from these showed only single binding sites, with cerebellar PSDs exhibiting lower KD values and a larger concentration of sites than did cerebral cortex PSDs. In the case of flunitrazepam, only one binding site was found for all four preparations, with cerebellar PSDs having twice the concentration of sites of cerebral PSDs. Photoaffinity labeling of the flunitrazepam receptor in PSDs resulted in the binding to a 51,000 Mr protein in both cases, with cerebellar PSDs again showing an increased concentration over that found in cerebral cortex PSDs. Based on this work, and on earlier work of ourselves and of others, we conclude that both populations of isolated PSDs contain inhibitory sites, but that the intact PSDs in both preparations are derived from Gray type I, probably excitatory, synapses, and that the inhibitory sites are found in the broken-up material in the PSD fractions which are derived from Gray type II, probably inhibitory, synapses.
采用从犬大脑皮层和小脑中分离出的突触膜和突触后致密物(PSD)进行[3H]GABA和[3H]氟硝西泮的结合实验。在大脑皮层膜中发现了两个GABA结合位点,而在小脑膜中仅发现一个。从这些组织中分离出的PSD仅显示单一结合位点,与大脑皮层PSD相比,小脑PSD的KD值更低,位点浓度更高。就氟硝西泮而言,在所有四种制剂中均仅发现一个结合位点,小脑PSD的位点浓度是大脑PSD的两倍。对PSD中氟硝西泮受体进行光亲和标记,结果在两种情况下均与一种51,000 Mr的蛋白质结合,小脑PSD的浓度再次高于大脑皮层PSD。基于这项工作以及我们自己和其他人早期的工作,我们得出结论,分离出的两种PSD群体均含有抑制性位点,但两种制剂中完整的PSD均源自I型灰质,可能是兴奋性突触,并且抑制性位点存在于PSD组分中破碎的物质中,这些物质源自II型灰质,可能是抑制性突触。