Isaacson J S, Solís J M, Nicoll R A
Physiology Graduate Program, University of California, San Francisco 94143-0450.
Neuron. 1993 Feb;10(2):165-75. doi: 10.1016/0896-6273(93)90308-e.
In the CNS, gamma-aminobutyric acid (GABA) acts as an inhibitory transmitter via ligand-gated GABAA receptor channels and G protein-coupled GABAB receptors. Both of these receptor types mediate inhibitory postsynaptic transmission in the hippocampus. In addition to these direct postsynaptic actions, GABAB receptor agonists inhibit excitatory transmission through presynaptic receptors on excitatory afferent terminals. However, a physiological role for the GABAB receptors on excitatory nerve endings has not been established. In this study, we have found a brief, heterosynaptic depression of excitatory synaptic transmission in the CA1 region of the hippocampal slice following short-lasting repetitive stimulation and determined that this inhibition is mediated by presynaptic GABAB receptors. The inhibition of GABA uptake greatly enhanced both the presynaptic action of GABA and the slow GABAB-mediated inhibitory postsynaptic current. Transmitter uptake was also found to regulate the "spill-over" of GABA at conventional GABAA synapses. These results suggest that uptake mechanisms restrict the spatial range of both point-to-point synaptic transmission mediated by GABA and its action at a distance.
在中枢神经系统中,γ-氨基丁酸(GABA)通过配体门控的GABAA受体通道和G蛋白偶联的GABAB受体发挥抑制性递质的作用。这两种受体类型均介导海马体中的抑制性突触后传递。除了这些直接的突触后作用外,GABAB受体激动剂还通过兴奋性传入终末上的突触前受体抑制兴奋性传递。然而,兴奋性神经末梢上GABAB受体的生理作用尚未明确。在本研究中,我们发现在短暂的重复刺激后,海马切片CA1区的兴奋性突触传递出现短暂的异突触抑制,并确定这种抑制是由突触前GABAB受体介导的。GABA摄取的抑制极大地增强了GABA的突触前作用以及缓慢的GABAB介导的抑制性突触后电流。还发现递质摄取可调节常规GABAA突触处GABA的“溢出”。这些结果表明,摄取机制限制了由GABA介导的点对点突触传递及其远距离作用的空间范围。