Beato Marco
Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6BT, United Kingdom.
J Neurosci. 2008 Jul 16;28(29):7412-25. doi: 10.1523/JNEUROSCI.0581-08.2008.
The concentration of transmitter in the synaptic cleft and its clearance time are one of the main determinants of synaptic strength. We estimated the time course of glycine at rat lumbar motoneurons synapses in spinal cord slices by recording synaptic currents in the presence of a low-affinity competitive antagonist at glycine receptors [2-(3-carboxypropyl)-3-amino-6-(4-methoxyphenyl)pyridazinium (SR-95531)]. Data were analyzed by using the established activation mechanism for glycine receptors and our measurements of SR-95531 binding rates. We show that this technique alone is not sufficient to determine simultaneously the peak concentration of transmitter and its clearance time. However, we found that block of the glial glycine transporter prolongs the glycine transient. This observation puts additional constraints on the range of possible values of the time course of glycine, indicating that glycine reaches a peak concentration of 2.2-3.5 mM and is cleared from the cleft with a time constant of 0.6-0.9 ms.
突触间隙中递质的浓度及其清除时间是突触强度的主要决定因素之一。我们通过在存在甘氨酸受体低亲和力竞争性拮抗剂[2-(3-羧丙基)-3-氨基-6-(4-甲氧基苯基)哒嗪鎓(SR-95531)]的情况下记录突触电流,来估计大鼠脊髓切片中腰段运动神经元突触处甘氨酸的时间进程。利用已确立的甘氨酸受体激活机制以及我们对SR-95531结合速率的测量对数据进行了分析。我们发现仅这项技术不足以同时确定递质的峰值浓度及其清除时间。然而,我们发现胶质细胞甘氨酸转运体的阻断会延长甘氨酸瞬变。这一观察结果对甘氨酸时间进程可能值的范围施加了额外限制,表明甘氨酸达到2.2 - 3.5 mM的峰值浓度,并以0.6 - 0.9 ms的时间常数从突触间隙清除。