Linden D J, Smeyne M, Connor J A
Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Neuron. 1993 Dec;11(6):1093-100. doi: 10.1016/0896-6273(93)90222-d.
Cerebellar long-term depression (LTD) is a persistent attenuation of the parallel fiber-Purkinje neuron (PF-PN) synapse induced by conjunctive stimulation of PF and climbing fiber (CF) inputs. A similar phenomenon is seen in the voltage-clamped PN in tissue culture when iontophoretic quisqualate application and PN depolarization are substituted for PF and CF stimulation, respectively. In this model, LTD induction requires activation of both AMPA and metabotropic receptors, together with PN depolarization. We have sought to determine the role of the AMPA receptor in LTD induction. The AMPA receptor does not appear to exert its effect by directly gating Ca2+ influx. Replacement of external Na+ during quisqualate/depolarization conjunction with permeant ions caused a blockade of LTD induction, suggesting that Na+ influx through the AMPA-associated channel is necessary for this process. Similarly, pairing quisqualate pulses with depolarizing steps near ENa also failed to induce LTD. The present results indicate that postsynaptic Na+ influx is necessary for LTD induction. While a portion of the relevant Na+ influx is provided by voltage-gated channels, the AMPA-associated ion channel is most important in this regard.
小脑长时程抑制(LTD)是平行纤维 - 浦肯野神经元(PF - PN)突触在PF和攀缘纤维(CF)输入联合刺激下引起的持续性减弱。当分别用离子电泳施加quisqualate和PN去极化替代PF和CF刺激时,在组织培养中电压钳制的PN中也能看到类似现象。在这个模型中,LTD诱导需要AMPA和代谢型受体的激活,以及PN去极化。我们试图确定AMPA受体在LTD诱导中的作用。AMPA受体似乎不是通过直接控制Ca2+内流来发挥作用。在quisqualate/去极化联合过程中用渗透性离子替代外部Na+会导致LTD诱导的阻断,这表明通过与AMPA相关的通道的Na+内流对于这个过程是必要的。同样,将quisqualate脉冲与接近ENa的去极化步骤配对也未能诱导LTD。目前的结果表明,突触后Na+内流对于LTD诱导是必要的。虽然一部分相关的Na+内流由电压门控通道提供,但在这方面与AMPA相关的离子通道最为重要。