McCain Katherine J, Petro Nathan M, Keil Andreas
Department of Psychology, University of Florida, Gainesville, Florida 32603.
Institute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, Nebraska 68010.
bioRxiv. 2025 May 13:2025.04.24.650318. doi: 10.1101/2025.04.24.650318.
The present study examined the contribution of the koniocellular retino-geniculate visual pathway to the electrocortical amplification of threat cues in human visual cortex using an aversive conditioning task. The task involved tritan stimuli, which are thought to convey visual information through S-cone signals that project to regions along the koniocellular pathway (tritan condition) and achromatic stimuli that preferentially activate luminance channels (luminance condition). Steady-state visual evoked potential (ssVEPs) responses to the conditioned threat (CS+) and safety cues (CS-) in each condition were analyzed using a non-parametric Bayesian bootstrapped approach. Results showed that the tritan and luminance conditions exhibited greater ssVEP responses to the CS+ compared to the CS- stimuli in occipital sensors early into the trial (0 ms - 1000 ms; logBF10 > 2, decisive support). In addition to these early conditioning effects, a late conditioning effect was observed (1500 ms - 2500 ms) in the tritan condition that emerged in bilateral anterior sensors (logBF10 > 2). To further examine the tritan contribution to aversive learning, transitive Bayes factors were computed to compare the magnitude of the conditioning effects across conditions. Transitive Bayes factors showed that the early conditioning effect was larger in the luminance condition compared to the tritan condition (logBF10 > 2). Furthermore, the late conditioning effect remained larger in the tritan condition compared to the luminance condition (logBF10 > 2). Our findings suggest that both the koniocellular visual pathway and luminance channels play a role in the electrocortical amplification of threat signals in human visual cortex.
本研究使用厌恶条件任务,检验了人类视觉皮层中短轴突视网膜 - 膝状体视觉通路对威胁线索的电皮质放大作用。该任务涉及蓝黄色刺激,据认为其通过投射到沿短轴突通路区域的S - 锥体信号传递视觉信息(蓝黄色条件),以及优先激活亮度通道的消色差刺激(亮度条件)。使用非参数贝叶斯自抽样方法分析了每种条件下对条件性威胁(CS +)和安全线索(CS -)的稳态视觉诱发电位(ssVEP)反应。结果显示,在试验早期(0毫秒 - 1000毫秒;对数贝叶斯因子10 > 2,决定性支持),与CS - 刺激相比,枕部传感器中蓝黄色和亮度条件下对CS + 的ssVEP反应更大。除了这些早期条件作用外,在蓝黄色条件下还观察到后期条件作用(1500毫秒 - 2500毫秒),出现在双侧前部传感器中(对数贝叶斯因子10 > 2)。为了进一步检验蓝黄色对厌恶学习的贡献,计算了传递贝叶斯因子以比较不同条件下条件作用效应的大小。传递贝叶斯因子表明,亮度条件下的早期条件作用效应比蓝黄色条件下更大(对数贝叶斯因子10 > 2)。此外,蓝黄色条件下的后期条件作用效应仍比亮度条件下更大(对数贝叶斯因子10 > 2)。我们的研究结果表明,短轴突视觉通路和亮度通道在人类视觉皮层中威胁信号的电皮质放大中均发挥作用。