Abstract

Neuropsychological and neuroimaging studies have suggested the presence of a fast, subcortical route for the processing of emotionally-salient visual information in the primate brain. This putative pathway consists of the superior colliculus (SC), pulvinar and amygdala. While the presence of such a pathway has been confirmed in sub-primate species, it has yet to be documented in the primate brain using conventional anatomical methods. We injected retrograde tracers into the amygdala and anterograde tracers into the colliculus, and examined regions of colocalization of these signals within the pulvinar of the macaque. Anterograde tracers injected into the SC labeled axonal projections within the pulvinar, primarily within the oral, lateral and medial subdivisions. These axonal projections from the colliculus colocalized with cell bodies within the pulvinar that were labeled by retrograde tracer injected into the lateral amygdala. This zone of overlap was most notable in the medial portions of the medial (PM), oral (PO) and inferior pulvinar (PI), and was often densely concentrated in the vicinity of the brachium of the SC. These data provide an anatomical basis for the previously suggested pathway mediating fast processing of emotionally salient information.

Highlights

  • Threatening stimuli require fast detection and response from an organism

  • The corresponding injection site in superior colliculus (SC) was localized to the lateral portion of stratum griseum intermedium (SGI), stratum album intermedium (SAI), stratum griseum profundum (SGP) and stratum album profundum (SAP)

  • We have shown a colocalization of projections from the SC with amygdala-projecting neurons in all nuclei of the macaque pulvinar, with the heaviest label occurring ventromedially in oral and portions of the medial (PM)

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Summary

Introduction

Threatening stimuli require fast detection and response from an organism. The canonical cortical visual processing stream refines information from coarse, low level representations in early cortical areas to detailed, high level information. In a non-conscious manner, patients with so-called ‘‘blindsight’’ can detect, localize, and distinguish between stimuli that are presented within the field of vision damaged by a lesion (Cowey and Stoerig, 1991; Sahraie et al, 1998). The LGN, which is the primary relay to visual cortex, projects to primary visual areas, and to higher order cortical regions (e.g., V4, MT; Born and Bradley, 2005). These extrastriate projections are likely preserved after damage to V1 (Schmid et al, 2009). Inactivation of either the LGN or the SC disrupts blindsight in macaques (Schmid et al, 2010; Kato et al, 2011; Takakuwa et al, 2017)

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