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1.
J Neurosci ; 2024 Sep 26.
Artículo en Inglés | MEDLINE | ID: mdl-39327005

RESUMEN

The prefrontal cortex is critical for decision-making across species, with its activity linked to choosing between options. Drift Diffusion Models (DDMs) are commonly employed to understand the neural computations underlying this behavior. Studies exploring the specific roles of regions of the rodent prefrontal cortex in controlling the decision process are limited. This study explored the role of the prelimbic cortex (PLC) in decision-making using a two-alternative forced-choice task. Rats first learned to report the location of a lateralized visual stimulus. The brightness of the stimulus indicated its reward value. Then, the rats learned to make choices between pairs of stimuli. Sex differences in learning were observed, with females responding faster and more selectively to high-value stimuli than males. DDM analysis found that males had decreased decision thresholds during initial learning, whereas females maintained a consistently higher drift rate. Pharmacological manipulations revealed that PLC inactivation reduced the decision threshold for all rats, indicating that less information was needed to make a choice in the absence of normal PLC processing. Mu opioid receptor stimulation of the PLC had the opposite effect, raising the decision threshold and reducing bias in the decision process towards high-value stimuli. These effects were observed without any impact on the rats' choice preferences. Our findings suggest that PLC has an inhibitory role in the decision process and regulates the amount of evidence that is required to make a choice. That is, PLC activity controls "when", but not "how", to act.Significance Statement This study reports causal evidence for a part of the rat prefrontal cortex, the prelimbic cortex, in controlling the amount of information needed to make a choice. Results were based on reversible inactivation using the GABA-A agonist muscimol and by stimulation of mu opioid receptors using intra-cortical infusions of the selective mu agonist DAMGO. We also found evidence for a sex difference in learning and performing a visually guided two-alternative forced-choice task. Drift Diffusion Models found that females had stable decision processes throughout learning, and showed a persistent bias against the lower value option. By contrast, males exhibited changes in their decision processes, notably reducing the amount of information needed to make choice over the period of early choice learning.

2.
bioRxiv ; 2024 Mar 19.
Artículo en Inglés | MEDLINE | ID: mdl-38562679

RESUMEN

The frontal cortex plays a critical role in decision-making. One specific frontal area, the anterior cingulate cortex, has been identified as crucial for setting a threshold for how much evidence is needed before a choice is made (Domenech & Dreher, 2010). Threshold is a key concept in drift diffusion models, a popular framework used to understand decision-making processes. Here, we investigated the role of the prelimbic cortex, part of the rodent cingulate cortex, in decision making. Male and female rats learned to choose between stimuli associated with high and low value rewards. Females learned faster, were more selective in their responses, and integrated information about the stimuli more quickly. By contrast, males learned more slowly and showed a decrease in their decision thresholds during choice learning. Inactivating the prelimbic cortex in female and male rats sped up decision making without affecting choice accuracy. Drift diffusion modeling found selective effects of prelimbic cortex inactivation on the decision threshold, which was reduced with increasing doses of the GABA-A agonist muscimol. Stimulating the prelimbic cortex through mu opioid receptors slowed the animals' choice latencies and increased the decision threshold. These findings provide the first causal evidence that the prelimbic cortex directly influences decision processes. Additionally, they suggest possible sex-based differences in early choice learning.

3.
iScience ; 27(6): 110044, 2024 Jun 21.
Artículo en Inglés | MEDLINE | ID: mdl-38883824

RESUMEN

The dorsolateral striatum (DLS) is important for performing actions persistently, even when it becomes suboptimal, reflecting a function that is reflexive and habitual. However, there are also ways in which persistent behaviors can result from a more prospective, planning mode of behavior. To help tease apart these possibilities for DLS function, we trained animals to perform a lever press for reward and then inhibited the DLS in key test phases: as the task shifted from a 1-press to a 3-press rule (upshift), as the task was maintained, as the task shifted back to the one-press rule (downshift), and when rewards came independent of pressing. During DLS inhibition, animals always favored their initially learned strategy to press just once, particularly so during the free-reward period. DLS inhibition surprisingly changed performance speed bidirectionally depending on the task shifts. DLS inhibition thus encouraged habitual behavior, suggesting it could normally help adapt to changing conditions.

4.
bioRxiv ; 2023 Jan 13.
Artículo en Inglés | MEDLINE | ID: mdl-36711550

RESUMEN

The dorsolateral striatum (DLS) is linked to the learning and honing of action routines. However, the DLS is also important for performing behaviors that have been successful in the past. The learning function can be thought of as prospective, helping to plan ongoing actions to be efficient and often optimal. The performance function is more retrospective, helping the animal continue to behave in a way that had worked previously. How the DLS manages this all is curious. What happens when a learned behavior becomes sub-optimal due to environment changes. In this case, the prospective function of the DLS would cause animals to (adaptively) learn and plan more optimal actions. In contrast, the retrospective function would cause animals to (maladaptively) favor the old behavior. Here we find that, during a change in learned task rules, DLS inhibition causes animals to adjust less rapidly to the new task (and to behave less vigorously) in a 'maladaptive' way. Yet, when the task is changed back to the initially learned rules, DLS inhibition instead causes a rapid and vigorous adjustment of behavior in an 'adaptive' way. These results show that inhibiting the DLS biases behavior towards initially acquired strategies, implying a more retrospective outlook in action selection when the DLS is offline. Thus, an active DLS could encourage planning and learning action routines more prospectively. Moreover, the DLS control over behavior can appear to be either advantageous/flexible or disadvantageous/inflexible depending on task context, and its control over vigor can change depending on task context. Significant Statement: Basal ganglia networks aid behavioral learning (a prospective planning function) but also favor the use of old behaviors (a retrospective performance function), making it unclear what happens when learned behaviors become suboptimal. Here we inhibit the dorsolateral striatum (DLS) as animals encounter a change in task rules, and again when they shift back to those learned task rules. DLS inhibition reduces adjustment to new task rules (and reduces behavioral vigor), but it increases adjustment back to the initially learned task rules later (and increases vigor). Thus, in both cases, DLS inhibition favored the use of the initially learned behavioral strategy, which could appear either maladaptive or adaptive. We suggest that the DLS might promote a prospective orientation of action control.

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