Beaumont K, Chilton W S, Yamamura H I, Enna S J
Brain Res. 1978 Jun 9;148(1):153-62. doi: 10.1016/0006-8993(78)90385-2.
[3H]Muscimol binding to crude synaptic membrane fractions of the rat central nervous is saturable with a high affinity dissociation constant of 2.2 nM. The regional distribution of this binding in rat brain and the effects of freezing, sodium and Triton X-100 are similar to those previously reported for [3H]GABA binding to the the synaptic GABA receptor site. Also, the substrate specificity of [3H]muscimol binding is identifical to that observed for the GABA receptor. Thus, [3H]muscimol is displaced, stereospecifically, only by those drugs and amino acids which are known to neurophysiologically interact with the synaptic GABA receptor but is unaffected by agents which activate or inhibit other neurotransmitter receptors. This suggests that the behavioral effects observed after the systemic administration of muscimol are probably the result of GABA receptor activation.
[3H]蝇蕈醇与大鼠中枢神经系统粗制突触膜组分的结合具有饱和性,其高亲和力解离常数为2.2 nM。这种结合在大鼠脑中的区域分布以及冷冻、钠和 Triton X - 100 的影响与先前报道的[3H]γ-氨基丁酸(GABA)与突触GABA受体位点的结合情况相似。此外,[3H]蝇蕈醇结合的底物特异性与GABA受体所观察到的相同。因此,[3H]蝇蕈醇仅被那些已知在神经生理学上与突触GABA受体相互作用的药物和氨基酸立体特异性地取代,但不受激活或抑制其他神经递质受体的药物影响。这表明全身给予蝇蕈醇后观察到的行为效应可能是GABA受体激活的结果。