cognitive control Flashcards
1
Q
Liebe (2012)
A
- monkeys performing visual WM task
- simultaneous recording from lateral PFC and V4
- increased synchrony between theta phases in PFC and V4 during delay period
- stronger synchrony when monkeys successfully maintained info in WM / remembered stimulus
- provides explanation of mechanism for how info is shared between both areas during maintenance of WM
- therefore how PFC exerts cognitive control over lower areas
2
Q
Pasternak (2015)
A
- delayed match-to-sample task with random dot stimuli of varying motion coherence
- lesion to lateral PFC impaired ability of monkeys to remember direction of motion, but didn’t depend on motion coherence (i.e. stimulus properties)
- also more impaired for same stimulus in certain locations
suggests PFC plays role in attending to stimuli and shifting attention to motion in other areas
3
Q
Postle (2006)
A
- retention of info in WM occurs alongside sustained activity in same brain regions responsible for representation of info in non-WM situations, so PFC is not simply a substrate for storage during WM
- instead, role of PFC is to employ control processes (e.g. attentional selection, flexible control etc) that are also required when performing WM task
- so PFC actively focuses attention on relevant sensory representation, selects info and performs executive functions necessary for cognitive processing of selected info
4
Q
Wallis (2001)
A
- single-cell recordings from PFC (dorsolateral, ventrolateral and orbitofrontal) of monkeys trained to use two abstract rules: indicate whether two images were same or different depending on current rule
- performed task with new images = shows general rule had been abstracted from previous experience
- 50% neurons showed higher activity for match rule and 50% for non-match = selective for specific rule
- ability to abstract rules from direct experience allows these rules to be applied to general situations = intelligent behaviour
5
Q
Asaad (2000)
A
- recordings from PFC neurons in 2 monkeys during 3 types of task: spatial, object and associative
- for many PFC neurons, activity was modulated by task being performed e.g. different baseline activity
- some neurons always active to same object regardless of task, others active to object only when certain behavioural response was required (so both sensory/perceptual and higher-level decision-making processes)
- increased neuronal activity in delay during object task: could represent impending choice / preparation, or could be inhibition of actions involved in the associative task for same object
6
Q
Milner 1963 / Dias 1997
A
- impairment on WCST is classic sign of PFC damage in humans
- unable to exert cognitive control / flexibly alter their responses to same stimuli depending on which rule is currently in effect
- Dias = primate analogue
7
Q
Miller (2000)
A
- humans don’t just reflexively react to immediate sensory info
- we have complex behaviours geared towards internally-generated and often far-removed goals
- mechanisms sculpted through experience/learning control lower-level sensory/motor operations for higher purpose
- forms basis of intelligent behaviour
- PFC must extract goal-relevant features of experiences that can be applied to future / abstract situations
- while HC binds stimuli into long-term memories consisting of specific episodes (e.g. Squire & Zola-Morgan 1991), PFC represents regularities in goals between different episodes = flexibility
- VTA dopaminergic neurons encode unexpected reward / reward prediction / prediction error so encode for associative learning
- DA influx affects plasticity by strengthening associative connections, and protects them against interference from distractors (maintain goal)
- PFC provides excitatory bias signals to other brain structures to flexibly guide flow of activity along task-relevant neural pathways (link to competition bias theory)
8
Q
Miller 1996
A
- sustained activity to sample in PFC may enhance responses to its repetition in inferior temporal cortex
- PFC therefore provides excitatory bias signals to other brain structures to flexibly guide flow of activity along task-relevant neural pathways (link to competition bias theory)
9
Q
Ragland (2015)
A
- fMRI and schizophrenic patients
- can engage VLPFC to provide control over semantic encoding of individual items
- but impaired at engaging DLPFC to provide more general control over all task items and only encode those that are task-appropriate
- therefore didn’t display improved episodic memory for target vs non-target items (whereas controls did)
- highlights differential roles for VLPFC and DLPFC in cognitive control
10
Q
Levy (2011)
A
- fMRI of right vlPFC
- inferior frontal junction (IFJ) = detection of behaviourally relevant stimuli (stopping and reflexive orienting)
- posterior areas of VLPFC = action updating
- other VLPFC areas = motor inhibition
- so has rich functional heterogeneity to allow for complex executive function
11
Q
Anderson (2001; 2016)
A
- DLPFC responsible for inhibitory control over behaviour via retrieval suppression (top-down modulation of HC activity) - although Aron (2007) argued against existence of this kind of inhibition
- form of executive control, prevents activation of HC episodic memories
process also implicated in forgetting
12
Q
Curtis & D’Esposito (2003)
A
DLPFC activation reflects top-down biasing control over posterior lower-level regions that store sensory representations = cognitive control during WM task
13
Q
Wager (2004)
A
fMRI showed lateral PFC more active when performing tasks that demand cognitive flexibility
14
Q
Damasio (1994)
A
- phineas gage: ventromedial PFC / OFC damage from tamping iron, loss of cognitive control
- impaired rational decision-making and processing of emotion = inappropriate behaviour in social situations (dysexecutive syndrome)
- impulsive, irresponsible
- but good performance on perceptual, memory and motor skills, and normal IQ
15
Q
Schoenbaum (2006)
A
- rats and outcome devaluation: food devaluated by adding poison
- despite showing they had learnt association between food and nausea (so had learned devaluation the same as normal rats), rats with OFC lesions still tried to get food
- inability to use stored memory of emotional event / outcome expectancies to guide action