Gautam Deepshila, Shields Abby, Krepps Emily, Ummear Raza Muhammad, Sivarao Digavalli V
Department of Pharmaceutical Sciences, Bill Gatton College of Pharmacy, East Tennessee State University, Johnson City, TN, United States.
Department of Pharmaceutical Sciences, Bill Gatton College of Pharmacy, East Tennessee State University, Johnson City, TN, United States.
Brain Res. 2024 Oct 15;1841:149091. doi: 10.1016/j.brainres.2024.149091. Epub 2024 Jun 17.
Auditory neural networks in the brain naturally entrain to rhythmic stimuli. Such synchronization is an accessible index of local network performance as captured by EEG. Across species, click trains delivered ∼ 40 Hz show strong entrainment with primary auditory cortex (Actx) being a principal source. Imaging studies have revealed additional cortical sources, but it is unclear if they are functionally distinct. Since auditory processing evolves hierarchically, we hypothesized that local synchrony would differ between between primary and association cortices. In female SD rats (N = 12), we recorded 40 Hz click train-elicited gamma oscillations using epidural electrodes situated at two distinct sites; one above the prefrontal cortex (PFC) and another above the Actx, after dosing with saline (1 ml/kg, sc) or the NMDA antagonist, MK801 (0.025, 0.05 or 0.1 mpk), in a blocked crossover design. Post-saline, both regions showed a strong 40 Hz auditory steady state response (ASSR). The latencies for the N1 response were ∼ 16 ms (Actx) and ∼ 34 ms (PFC). Narrow band (38-42 Hz) gamma oscillations appeared rapidly (<40 ms from stim onset at Actx but in a more delayed fashion (∼200 ms) at PFC. MK801 augmented gamma synchrony at Actx while dose-dependently disrupting at the PFC. Event-related gamma (but not beta) coherence, an index of long-distance connectivity, was disrupted by MK801. In conclusion, local network gamma synchrony in a higher order association cortex performs differently from that of the primary auditory cortex. We discuss these findings in the context of evolving sound processing across the cortical hierarchy.
大脑中的听觉神经网络会自然地与节律性刺激同步。这种同步是脑电图所捕捉到的局部网络性能的一个可获取指标。在所有物种中,以约40赫兹频率传递的点击序列显示出强烈的同步,初级听觉皮层(Actx)是主要来源。成像研究揭示了其他皮层来源,但尚不清楚它们在功能上是否有区别。由于听觉处理是分层发展的,我们推测初级皮层和联合皮层之间的局部同步会有所不同。在雌性SD大鼠(N = 12)中,我们采用阻断交叉设计,在给予生理盐水(1毫升/千克,皮下注射)或NMDA拮抗剂MK801(0.025、0.05或0.1毫克/千克)后,使用置于两个不同部位的硬膜外电极记录40赫兹点击序列诱发的伽马振荡;一个位于前额叶皮层(PFC)上方,另一个位于Actx上方。注射生理盐水后,两个区域均显示出强烈的40赫兹听觉稳态反应(ASSR)。N1反应的潜伏期在Actx约为16毫秒,在PFC约为34毫秒。窄带(38 - 42赫兹)伽马振荡迅速出现(在Actx刺激开始后<40毫秒,但在PFC出现得更延迟(约200毫秒)。MK801增强了Actx处的伽马同步,同时在PFC处呈剂量依赖性地破坏伽马同步。事件相关伽马(而非贝塔)相干性是远距离连接的一个指标,被MK801破坏。总之,高级联合皮层中的局部网络伽马同步与初级听觉皮层的表现不同。我们在整个皮层层次结构中不断演变的声音处理背景下讨论这些发现。