Beckman Institute, University of Illinois at Urbana-Champaign, Urbana, IL 61801.
Department of Comparative Biosciences, College of Veterinary Medicine, University of Illinois at Urbana-Champaign, Urbana, IL 61802.
eNeuro. 2021 Feb 1;8(1). doi: 10.1523/ENEURO.0321-20.2021. Print 2021 Jan-Feb.
Polychlorinated biphenyls (PCBs) are enduring environmental toxicants and exposure is associated with neurodevelopmental deficits. The auditory system appears particularly sensitive, as previous work has shown that developmental PCB exposure causes both hearing loss and gross disruptions in the organization of the rat auditory cortex. However, the mechanisms underlying PCB-induced changes are not known, nor is it known whether the central effects of PCBs are a consequence of peripheral hearing loss. Here, we study changes in both peripheral and central auditory function in rats with developmental PCB exposure using a combination of optical and electrophysiological approaches. Female rats were exposed to an environmental PCB mixture in utero and until weaning. At adulthood, auditory brainstem responses (ABRs) were measured, and synaptic currents were recorded in slices from auditory cortex layer 2/3 neurons. Spontaneous IPSCs (sIPSCs) and miniature IPSCs (mIPSCs) were more frequent in PCB-exposed rats compared with controls and the normal relationship between IPSC parameters and peripheral hearing was eliminated in PCB-exposed rats. No changes in spontaneous EPSCs were found. Conversely, when synaptic currents were evoked by laser photostimulation of caged-glutamate, PCB exposure did not affect evoked inhibitory transmission, but increased the total excitatory charge, the number and distance of sites that evoke a significant response. Together, these findings indicate that early developmental exposure to PCBs causes long-lasting changes in both inhibitory and excitatory neurotransmission in the auditory cortex that are independent of peripheral hearing changes, suggesting the effects are because of the direct impact of PCBs on the developing auditory cortex.
多氯联苯 (PCBs) 是持久的环境毒物,接触这些毒物与神经发育缺陷有关。听觉系统似乎特别敏感,因为之前的工作表明,发育性 PCB 暴露会导致听力损失和大鼠听觉皮层组织的严重紊乱。然而,PCBs 引起的变化的机制尚不清楚,也不知道 PCBs 的中枢效应是否是外周听力损失的结果。在这里,我们使用光学和电生理方法相结合,研究了发育性 PCB 暴露大鼠的外周和中枢听觉功能变化。雌性大鼠在子宫内和断奶前暴露于环境 PCB 混合物中。成年后,测量听觉脑干反应 (ABR),并在听觉皮层 2/3 层神经元的切片中记录突触电流。与对照组相比,PCB 暴露大鼠的自发 IPSC(sIPSC) 和微小 IPSC(mIPSC) 更为频繁,并且在 PCB 暴露大鼠中消除了 IPSC 参数与外周听力之间的正常关系。未发现自发 EPSC 有变化。相反,当通过笼状谷氨酸的激光光刺激诱发突触电流时,PCB 暴露不会影响诱发的抑制性传递,但增加了总兴奋性电荷、引起显著反应的位点的数量和距离。总之,这些发现表明,早期发育性 PCB 暴露会导致听觉皮层中抑制性和兴奋性神经传递的持久变化,而与外周听力变化无关,这表明这些效应是因为 PCBs 对发育中的听觉皮层的直接影响。