Isolating the Contribution of the Koniocellular Visual Pathway in Aversive Learning in Human Visual Cortex
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The present study examined how the koniocellular retino-geniculate visual pathway contributes to the electrocortical amplification of threat cues in human visual cortex using a simple aversive conditioning task. The task involved S-cone isolating stimuli (Tritan condition) and achromatic luminance stimuli (luminance condition) that preferentially activated the koniocellular pathway and luminance channels, respectively. Steady-state visual evoked potential (ssVEPs) responses to the conditioned threat cues (CS+) and safety cues (CS-) in each condition were analyzed using a non-parametric Bayesian bootstrapped approach. The Tritan and luminance conditions exhibited greater ssVEP responses to the CS+ stimuli compared to the CS-stimuli in occipital sensors early into the trial (0 ms - 1000 ms; logBF10 > 2). In addition to these early conditioning effects, a late conditioning effect was observed (1500 ms - 2500 ms) in the Tritan condition that emerged over bilateral anterior sensors (logBF10 > 2). To further examine the koniocellular contribution to aversive learning, transitive Bayes factors were computed to compare the magnitude of the conditioning effects across conditions. Transitive Bayesian comparisons showed that the early conditioning effect was larger for the luminance condition than for the Tritan condition (logBF10 > 2). Furthermore, the late conditioning effect remained larger in the Tritan condition compared to the luminance condition (logBF10 > 2). Our results are consistent with previous work demonstrating that Tritan stimuli elicit enhanced electrocortical responses and with theoretical notions suggesting that the koniocellular pathway contributes to the representation of threat signals in human visual cortex.
Significance Statement
The functional roles of the koniocellular retino-geniculate pathway in human visual processing are topics of much interest. However, the extent that the koniocellular pathway contributes to the amplification of threat signals in the human visual cortex remains unclear. Therefore, the present study examined the contribution of the koniocellular pathway in aversive learning in humans using neurophysiological recordings. Our findings indicate that the koniocellular visual pathway plays a role in the electrocortical amplification of threat signals in humans and extends our growing understanding of the functional properties of the koniocellular pathway.