Jones M V, Westbrook G L
Vollum Institute, Oregon Health Sciences University, Portland 97201, USA.
Neuron. 1995 Jul;15(1):181-91. doi: 10.1016/0896-6273(95)90075-6.
We studied the role of desensitization at inhibitory synapses by comparing nonequilibrium GABAA channel gating with inhibitory postsynaptic currents (IPSCs). Currents activated by brief pulses of 1-10 mM GABA to outside-out patches from cultured hippocampal neurons mimicked GABA-mediated IPSCs. Although the average open time of single GABAA channels following brief pulses was less than 10 ms, channels entered long (tau = 38-69 ms) closed states and subsequently reopened. Movement through these states resulted in paired-pulse desensitization. The time required for deactivation after removal of agonist also increased in proportion to the extent of desensitization. These results suggest that visits to desensitized states buffer the channel in bound conformations and underlie the expression of long-lasting components of the IPSC. Reopening after GABAA receptor desensitization may thus enhance inhibitory synaptic transmission by prolonging the response to a brief synaptic GABA transient.
我们通过比较非平衡GABAA通道门控与抑制性突触后电流(IPSCs),研究了脱敏在抑制性突触中的作用。用1-10 mM GABA的短脉冲激活培养的海马神经元外翻膜片上的电流,模拟了GABA介导的IPSCs。尽管短脉冲后单个GABAA通道的平均开放时间小于10毫秒,但通道进入长(τ = 38-69毫秒)关闭状态并随后重新开放。通过这些状态的转换导致了双脉冲脱敏。去除激动剂后失活所需的时间也与脱敏程度成比例增加。这些结果表明,进入脱敏状态会使通道处于结合构象中,这是IPSC持久成分表达的基础。因此,GABAA受体脱敏后的重新开放可能通过延长对短暂突触GABA瞬变的反应来增强抑制性突触传递。