Kawaguchi S, Hirano T
Department of Biophysics, Graduate School of Science, Kyoto University, Japan.
Neuron. 2000 Aug;27(2):339-47. doi: 10.1016/s0896-6273(00)00041-6.
At inhibitory synapses on a cerebellar Purkinje neuron, the depolarization caused by heterosynaptic climbing fiber activation induces long-lasting potentiation accompanied by an increase in GABA(A) receptor responsiveness. Here we show that activation of a presynaptic inhibitory interneuron during the conditioning postsynaptic depolarization suppresses the potentiation. The suppression is due to postsynaptic GABA(B) receptor activation by GABA released from presynaptic terminals. The results suggest that GABA(B) receptor activation decreases the activity of cAMP-dependent protein kinase through the G(i)/G(o) proteins. The presynaptic activity-dependent suppression of synaptic plasticity is a novel regulatory mechanism of synaptic efficacy at individual synapses and may contribute to the learning and computational ability of the cerebellar cortex.
在小脑浦肯野神经元的抑制性突触处,由异突触攀缘纤维激活引起的去极化诱导了长时程增强,并伴有GABA(A)受体反应性增加。我们在此表明,在条件性突触后去极化期间,突触前抑制性中间神经元的激活会抑制这种增强。这种抑制是由于突触前终末释放的GABA激活了突触后GABA(B)受体。结果表明,GABA(B)受体激活通过G(i)/G(o)蛋白降低了cAMP依赖性蛋白激酶的活性。突触前活动依赖性对突触可塑性的抑制是单个突触处突触效能的一种新型调节机制,可能有助于小脑皮质的学习和计算能力。