Murashima M, Hirano T
Department of Biophysics, Graduate School of Science, Kyoto University, Sakyo-ku, Kyoto 606-8502, Japan.
J Neurosci. 1999 Sep 1;19(17):7326-33. doi: 10.1523/JNEUROSCI.19-17-07326.1999.
The cerebellar long-term depression (LTD) is the long-lasting reduction of transmission efficacy at the granule neuron-Purkinje neuron (G-P) synapses and is a candidate mechanism for the motor learning. Despite extensive studies on its induction and expression mechanisms, it has not been known how long the LTD lasts. The LTD is accompanied by the decrease in the postsynaptic responsiveness to glutamate, the transmitter at G-P synapses. Therefore, during the LTD, the amplitude of miniature EPSCs (mEPSCs) at G-P synapses should decrease. We studied the depression of mEPSC amplitudes (DME) as a possible contributing factor for the LTD and found that the conditioning treatment of cultured cerebellar neurons with 50 mM K(+) and 100 microM glutamate, an analogous condition used to induce the LTD, induced the long-lasting DME. The mEPSC amplitudes recovered to the original level 48 hr after the 5 min conditioning treatment. Changing the duration of the conditioning revealed that the DME consisted of two distinct phases: the early phase lasting for a few hours and the late phase for >1 d. The latter was distinguished from the former by its requirement of prolonged conditioning treatment and syntheses of mRNA and protein for the induction. There were critical periods for mRNA and protein syntheses. The critical period for protein synthesis was much longer than that for mRNA synthesis. These results demonstrate that the DME lasts for 1-2 d and that it consists of two phases, whose induction and maintenance mechanisms are distinct.
小脑长时程抑制(LTD)是颗粒神经元 - 浦肯野神经元(G - P)突触处传递效能的长期降低,是运动学习的一种潜在机制。尽管对其诱导和表达机制进行了广泛研究,但LTD持续多长时间尚不清楚。LTD伴随着突触后对谷氨酸(G - P突触处的递质)反应性的降低。因此,在LTD期间,G - P突触处微小兴奋性突触后电流(mEPSCs)的幅度应会降低。我们研究了mEPSC幅度降低(DME)作为LTD可能的促成因素,发现用50 mM K⁺和100 μM谷氨酸对培养的小脑神经元进行条件处理(一种用于诱导LTD的类似条件)可诱导长期的DME。在5分钟的条件处理后48小时,mEPSC幅度恢复到原始水平。改变条件处理的持续时间表明,DME由两个不同阶段组成:早期阶段持续数小时,晚期阶段持续超过1天。后者与前者的区别在于其需要延长的条件处理以及诱导所需的mRNA和蛋白质合成。mRNA和蛋白质合成存在关键时期。蛋白质合成的关键时期比mRNA合成的关键时期长得多。这些结果表明,DME持续1 - 2天,且由两个阶段组成,其诱导和维持机制不同。