Pastuszko A, Wilson D F, Erecińska M
FEBS Lett. 1984 Nov 19;177(2):249-54. doi: 10.1016/0014-5793(84)81293-4.
Thiopental, a thiobarbiturate which partitions prefentially into the hydrophobic environment, inhibited transport of amino acid neurotransmitters, GABA, aspartate and glutamate, and of biogenic amine, dopamine, across the synaptosomal membrane. At a given protein and thiopental concentration GABA transport was more sensitive to the barbiturate than were the movements of aspartate and glutamate although the uptake of each amino acid was inhibited essentially to the same extent as was its K+-stimulated release. By contrast, inhibition of dopamine uptake was larger than that of its release. Thiopental also inhibited the release of amino acid neurotransmitters caused by anaerobiosis. It is suggested that the barbiturate modifies the properties of the synaptosomal lipids and/or hydrophobic segments of proteins and thereby, simultaneously and independently, affects various membrane functions. The equal inhibition of uptake and release of amino acid neurotransmitters is consistent with the postulate that their transport occurs through the reversible membrane carriers which function efficiently in both the inward and outward directions.
硫喷妥钠是一种硫代巴比妥酸盐,它优先分布于疏水环境中,抑制氨基酸神经递质γ-氨基丁酸(GABA)、天冬氨酸和谷氨酸以及生物胺多巴胺跨突触体膜的转运。在给定的蛋白质和硫喷妥钠浓度下,GABA转运对巴比妥酸盐的敏感性高于天冬氨酸和谷氨酸的转运,尽管每种氨基酸的摄取受到的抑制程度与钾离子刺激的释放受到的抑制程度基本相同。相比之下,多巴胺摄取的抑制作用大于其释放的抑制作用。硫喷妥钠还抑制无氧状态引起的氨基酸神经递质的释放。有人认为,巴比妥酸盐改变了突触体脂质和/或蛋白质疏水片段的性质,从而同时且独立地影响各种膜功能。氨基酸神经递质摄取和释放受到同等抑制,这与它们的转运通过可逆膜载体进行的假设一致,这些载体在向内和向外方向上均能高效发挥作用。