Department of Neurosciences, University of New Mexico School of Medicine, Albuquerque, NM 87131, USA.
Department of Neurosurgery, University of New Mexico School of Medicine, Albuquerque, NM 87131, USA.
Neuroscience. 2024 Jul 23;551:323-332. doi: 10.1016/j.neuroscience.2024.05.035. Epub 2024 May 29.
Spreading depolarization (SD) is a slowly propagating wave of prolonged activation followed by a period of synaptic suppression. Some prior reports have shown potentiation of synaptic transmission after recovery from synaptic suppression and noted similarities with the phenomenon of long-term potentiation (LTP). Since SD is increasingly recognized as participating in diverse neurological disorders, it is of interest to determine whether SD indeed leads to a generalized and sustained long-term strengthening of synaptic connections. We performed a characterization of SD-induced potentiation, and tested whether distinctive features of SD, including adenosine accumulation and swelling, contribute to reports of SD-induced plasticity. Field excitatory postsynaptic potentials (fEPSPs) were recorded in the hippocampal CA1 subregion of murine brain slices, and SD elicited using focal microinjection of KCl. A single SD was sufficient to induce a consistent potentiation of slope and amplitude of fEPSPs. Both AMPA- and NMDA-receptor mediated components were enhanced. Potentiation peaked ∼20 min after SD recovery and was sustained for ∼30 min. However, fEPSP amplitude and slope decayed over an extended 2-hour recording period and was estimated to reach baseline after ∼3 h. Potentiation was saturated after a single SD and adenosine A1 receptor activation did not mask additional potentiation. Induction of LTP with theta-burst stimulation was not altered by prior induction of SD and molecular mediators known to block LTP induction did not block SD-induced potentiation. Together, these results indicate an intermediate duration potentiation that is distinct from hippocampal LTP and may have implications for circuit function for 1-2 h following SD.
去极化扩散(SD)是一种缓慢传播的激活波,随后是一段突触抑制期。一些先前的报告显示,在突触抑制恢复后,突触传递增强,并注意到与长时程增强(LTP)现象的相似性。由于 SD 越来越被认为参与了多种神经疾病,因此确定 SD 是否确实导致突触连接的普遍和持续长期增强是很有意义的。我们对 SD 诱导的增强进行了表征,并测试了 SD 特有的特征,包括腺苷积累和肿胀,是否有助于解释 SD 诱导的可塑性。在鼠脑切片的海马 CA1 亚区记录场兴奋性突触后电位(fEPSP),并通过 KCl 局灶微注射诱导 SD。单次 SD 足以引起 fEPSP 斜率和幅度的一致增强。AMPA 和 NMDA 受体介导的成分都增强了。增强在 SD 恢复后约 20 分钟达到峰值,并持续约 30 分钟。然而,fEPSP 幅度和斜率在长达 2 小时的记录期间衰减,并估计在约 3 小时后达到基线。增强在单次 SD 后达到饱和,并且腺苷 A1 受体激活不会掩盖额外的增强。与先前诱导的 SD 相比,θ爆发刺激诱导的 LTP 没有改变,并且已知阻断 LTP 诱导的分子介质也没有阻断 SD 诱导的增强。这些结果共同表明存在一种中间持续时间的增强,与海马体 LTP 不同,并且可能对 SD 后 1-2 小时的电路功能有影响。