Search bioRxiv⌕ Search

bioRxiv · 10.1101/097410

When Attended and Conscious Perception Deactivates Fronto-Parietal Regions

Abstract

Conscious and attended perception is commonly thought to elicit fronto-parietal activity. However, supportive evidence comes largely from studies which involve detecting a target and reporting its visibility. This approach confounds conscious perception with goal completion of either the perceptual task of detection or the metacognitive task of introspective reporting. In contrast, in real life such perceptions are a means of achieving goals and rarely a goal in themselves, and almost never involve explicit metacognitive reports. It therefore remains unclear if fronto-parietal activity is indeed a correlate of conscious perception or is the result of confounds related to goal completion. Here we show that conscious and attended perception when delinked from goals does not increase fronto-parietal activity, and when inconsequential for the goal may even deactivate these regions. In experiments 1 and 2 participants attended to a highly visible stream of letters to detect the occasional targets in their midst. The non-target letters, in spite of being visible and attended to, deactivated fronto-parietal regions. In experiment 3 we looked at the activity elicited by a loud auditory cue that had to be kept in memory for up to 9 s and used to select the correct rule for completing the goal. Even such a salient, attended and remembered event did not elicit prefrontal activity. Across these experiments conscious and attended perception only activated the relevant sensory regions while goal completion events activated fronto-parietal regions.\n\nSignificance statementConsciousness and attended perception has been seen to correlate with fronto-parietal activity. This informs key theories of consciousness and attention, e.g. widespread availability of incoming information or its higher level representation causes perceptual awareness, or that top down attention during perception broadcasts incoming sensations into frontal and parietal regions. However such experiments unwittingly conflate attended and conscious perception with some form of goal completion, whereas such perception in our daily life mostly serves as a means of goal completion and not a goal in itself. Here we show that such perception when delinked from goal completion does not activate fronto-parietal regions, and may even deactivate these regions if the percept is inconsequential for goal completion.

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Farooqui, A. A., Manly, T.. 2016-12-30. When Attended and Conscious Perception Deactivates Fronto-Parietal Regions. https://doi.org/10.1101/097410

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Sex differences in fear extinction are conditional, not categorical

Threat memories are dynamic, and their behavioral expression can change with subsequent experience and the passage of time. Extinction training can reduce conditioned fear responses, yet these responses may re-emerge over time through spontaneous recovery. Although biological sex has been implicated as modulatory factor in fear and extinction memory processes, studies have reported inconsistent findings. Here, we investigated how differences in extinction training and the timing of memory assessment influence extinction memory in male and female mice. Using contextual fear conditioning, we assessed fear acquisition and threat retention, characterized within-session and across-session extinction during repeated training, and compared shorter (3-minute) and longer (6-minute) daily extinction sessions. We subsequently evaluated extinction memory retention and spontaneous recovery at a later time point. Estrous-cycle stage in females was monitored daily throughout the experimental protocol to examine its potential association with fear and extinction behavior. We found that males and females demonstrated comparable fear acquisition and threat memory, as well as similar extinction progression across days. During longer extinction sessions, but not shorter, males showed greater within-session reductions in freezing, whereas females exhibited modestly higher overall freezing. We found no significant sex difference in the magnitude of spontaneous recovery. There was no significant association between estrous-cycle stage and freezing behavior. Together, our findings suggest that sex-dependent differences in contextual fear extinction are not uniformly expressed, but rather depend on the experimental conditions under which extinction is assessed

neuroscience↗

LAMA2-related muscular dystrophy alters Schwann cell calcium homeostasis and increases peripheral nerve inflammation

LAMA2-related muscular dystrophy (LAMA2-RD) affects skeletal muscle and peripheral nerves, yet the consequences of LAMA2 deficiency on peripheral nerve integrity beyond early postnatal development remain incompletely understood. We investigated sciatic nerve architecture and molecular alterations across postnatal life in hypomorphic Lama2dy2J/dy2J mice. LAMA2 localizes around the abaxonal surface of myelinating Schwann cells in control nerves. LAMA2-deficient nerves exhibited patchy regions lacking myelinated axons from early postnatal stages into adulthood, including expanded Remak bundles along with axons completely lacking normal Schwann cell ensheathment. In adult nerves, myelin infolding and reduced myelin circularity revealed abnormalities in the architecture of myelin that had formed. Bulk sciatic nerve RNA sequencing identified altered calcium-signaling and immune-related transcriptional signatures. Complementary Fura Red measurements in primary nerve-derived Schwann cell cultures demonstrated decreased intracellular calcium in LAMA2-deficient samples, while ATP-evoked responses were preserved. Older LAMA2-deficient nerves also exhibited increased CD45+CD11b+ myeloid-cell infiltration. Together, these observations extend the characterization of LAMA2-associated neuropathy into adulthood and identify calcium homeostasis and neuroimmune responses as candidate processes relevant to persistent peripheral nerve pathology.

neuroscience↗

Endothelin-1 from Tongue Glands Gates 1 Sodium Taste and Intake

Sodium is an essential nutrient. To survive sodium deficiency, animals dramatically increase their appetite for salt. However, whether and how sodium depletion impacts the taste of salt to drive sodium intake is unknown. Here we show that tongue gland-derived endothelin-1 (EDN1) regulates the amiloride-sensitive, sodium-selective salt taste. Edn1 is specifically expressed in the glands embedded within the tongue. Under normal conditions, EDN1 suppresses salt taste by acting on its receptor EDNRB on the projections of salt-sensing taste neurons innervating taste buds. When internal sodium levels drop, EDN1 expression decreases, lifting this inhibition and enhancing responses to salt. Applying EDN1 directly to the tongue, using a nonionic eutectic-based organogel (Neogel) delivery technology that we establish here, dampens the activity of the salt-sensing taste neurons and reduces salt intake and preference. Conversely, genetic deletion of Ednrb in taste neurons mimics the effects of sodium deficiency, enhancing salt-sensing neuron activity and increasing salt consumption. These findings reveal a peripheral mechanism that regulates salt taste and intake in response to internal sodium levels, highlighting a direct role of the taste pathway in maintaining nutrient homeostasis.

neuroscience↗