Basolateral amygdala oscillations enable fear learning in a biophysical model DOI Open Access
Anna Cattani, Don B. Arnold, Michelle M. McCarthy

и другие.

Опубликована: Ноя. 4, 2024

The basolateral amygdala (BLA) is a key site where fear learning takes place through synaptic plasticity. Rodent research shows prominent low theta (∼3-6 Hz), high (∼6-12 and gamma (>30 Hz) rhythms in the BLA local field potential recordings. However, it not understood what role these play supporting Here, we create biophysically detailed model of circuit to show that several classes interneurons (PV, SOM, VIP) can be critically involved producing rhythms; promote formation dedicated shaped spike-timing-dependent Each class necessary for We find rhythm biomarker successful conditioning. makes use commonly found cortex and, hence, may apply wide variety associative situations.

Язык: Английский

Deciphering neuronal variability across states reveals dynamic sensory encoding DOI Creative Commons
Shailaja Akella, Peter Ledochowitsch, Joshua H. Siegle

и другие.

Nature Communications, Год журнала: 2025, Номер 16(1)

Опубликована: Фев. 19, 2025

Язык: Английский

Процитировано

0

Bilateral integration in somatosensory cortex is controlled by behavioral relevance DOI
Hyein Park, Hayagreev V. S. Keri,

Chaeyoung Yoo

и другие.

Nature Neuroscience, Год журнала: 2025, Номер unknown

Опубликована: Май 14, 2025

Язык: Английский

Процитировано

0

Diversity of omission responses to visual images across brain-wide regions DOI
Noam Nitzan, György Buzsáki

Science Advances, Год журнала: 2025, Номер 11(21)

Опубликована: Май 21, 2025

An organism’s survival depends on its ability to anticipate forthcoming events and detect discrepancies between the expected actual sensory inputs. We analyzed data from mice performing a visual go/no-go change-detection task where sequence of stimulus presentations was intermittently interrupted by omission stimulus. The did not elicit discernable spiking responses in cortical neurons. Instead, firing rates image presentations, including period, ramped linearly without interruption at time omitted image. Several neuron types cortex neurons were identified with various images their omissions. A minority cells nonvisual areas, hippocampus, increased onset even when these respond images. Our study elucidates origin sheds light role hippocampal subcortical circuits detection.

Язык: Английский

Процитировано

0

Coordinated changes in a cortical circuit sculpt effects of novelty on neural dynamics DOI Creative Commons
Shinya Ito, Alex T. Piet, Corbett Bennett

и другие.

Cell Reports, Год журнала: 2024, Номер 43(9), С. 114763 - 114763

Опубликована: Сен. 1, 2024

Recent studies have found dramatic cell-type-specific responses to stimulus novelty, highlighting the importance of analyzing cortical circuitry at this granularity understand brain function. Although initial work characterized activity by cell type, alterations in due interacting novelty effects remain unclear. We investigated circuit mechanisms underlying observed neural dynamics response novel stimuli using a large-scale public dataset electrophysiological recordings behaving mice and population network model. The model was constrained multi-patch synaptic physiology electron microscopy data. generally weaker connections under stimuli, with shifts balance between somatostatin (SST) vasoactive intestinal polypeptide (VIP) populations increased excitatory influences on parvalbumin (PV) SST populations. These findings systematically characterize how circuits adapt novelty.

Язык: Английский

Процитировано

1

Basolateral amygdala oscillations enable fear learning in a biophysical model DOI Creative Commons
Anna Cattani, Don B. Arnold, Michelle M. McCarthy

и другие.

eLife, Год журнала: 2024, Номер 12

Опубликована: Ноя. 26, 2024

The basolateral amygdala (BLA) is a key site where fear learning takes place through synaptic plasticity. Rodent research shows prominent low theta (~3–6 Hz), high (~6–12 and gamma (>30 Hz) rhythms in the BLA local field potential recordings. However, it not understood what role these play supporting Here, we create biophysically detailed model of circuit to show that several classes interneurons (PV, SOM, VIP) can be critically involved producing rhythms; promote formation dedicated shaped spike-timing-dependent Each class necessary for We find rhythm biomarker successful conditioning. makes use commonly found cortex and, hence, may apply wide variety associative situations.

Язык: Английский

Процитировано

1

Basolateral amygdala oscillations enable fear learning in a biophysical model DOI Creative Commons
Anna Cattani, Don B. Arnold, Michelle M. McCarthy

и другие.

eLife, Год журнала: 2023, Номер 12

Опубликована: Авг. 14, 2023

The basolateral amygdala (BLA) is a key site where fear learning takes place through synaptic plasticity. Rodent research shows prominent low theta (~3–6 Hz), high (~6–12 and gamma (>30 Hz) rhythms in the BLA local field potential recordings. However, it not understood what role these play supporting Here, we create biophysically detailed model of circuit to show that several classes interneurons (PV, SOM, VIP) can be critically involved producing rhythms; promote formation dedicated shaped spike-timing-dependent Each class necessary for We find rhythm biomarker successful conditioning. makes use commonly found cortex and, hence, may apply wide variety associative situations.

Язык: Английский

Процитировано

2

Basolateral amygdala oscillations enable fear learning in a biophysical model DOI Creative Commons
Anna Cattani, Don B. Arnold, Michelle M. McCarthy

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2023, Номер unknown

Опубликована: Апрель 28, 2023

Abstract The basolateral amygdala (BLA) is a key site where fear learning takes place through synaptic plasticity. Rodent research shows prominent low theta (∼3-6 Hz), high (∼6-12 and gamma (>30 Hz) rhythms in the BLA local field potential recordings. However, it not understood what role these play supporting Here, we create biophysically detailed model of circuit to show that several classes interneurons (PV, SOM, VIP) can be critically involved producing rhythms; promote formation dedicated shaped spike-timing-dependent Each class necessary for We find rhythm biomarker successful conditioning. makes use commonly found cortex and, hence, may apply wide variety associative situations. Significance Our paper accounts experimental evidence showing amygdalar exist, suggests network origins rhythms, points their central mechanisms plasticity learning. It one few papers address high-order cognition with models, which are sometimes thought too adequately constrained. provides template how information about brain constrain biophysical models. detail, first time, multiple help provide time scales some kinds (STDP). spells out conditions under such interactions between needed STDP why. Finally, our work helps framework by discrepancies literature might reevaluated. In particular, discuss issues Hebbian learning; context neuromodulation resolve those issues. addresses more general than since based on cortex, as well amygdala.

Язык: Английский

Процитировано

1

Selective engagement of prefrontal VIP neurons in reversal learning DOI Creative Commons
Jee Hyun Yi, Young Ju Yoon, Huijeong Jeong

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown

Опубликована: Апрель 5, 2024

ABSTRACT To gain insights into neural mechanisms enabling behavioral adaptations to complex and multidimensional environmental dynamics, we examined roles of VIP neurons in mouse medial prefrontal cortex (mPFC) probabilistic reversal learning. Behaviorally, manipulating neuronal activity left classical conditioning unaffected but severely impaired Physiologically, conditioned cue-associated responses changed abruptly after encountering an unexpected reward. They also conveyed strong reward prediction error signals during reversal, not before or after, unlike pyramidal which consistently throughout all phases. Furthermore, the signal’s persistence across trials correlated with learning duration. These results suggest that mPFC play crucial rapid learning, incremental cue-outcome association by monitoring significant deviations from ongoing contingency imposing error-correction adjustments. findings shed light on intricate cortical circuit dynamics underpinning flexibility complex, multifaceted environments.

Язык: Английский

Процитировано

0

Bilateral integration in somatosensory cortex is controlled by behavioral relevance DOI Creative Commons

Hyein Park,

Hayagreev V. S. Keri,

Chaeyoung Yoo

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown

Опубликована: Июнь 1, 2024

Abstract Sensory perception naturally requires processing stimuli from both sides of the body. Yet, how neurons bind stimulus features across hemispheres to create a unified perceptual experience remains unknown. To address this question, we performed large-scale recordings in somatosensory cortices (S1) while mice shared information between their and discriminated two categories bilateral stimuli. When expert touched associated with reward, they moved whiskers greater symmetry. During period, synchronous spiking enhanced spike-field coupling emerged hemispheres. This coordinated activity was absent stimulus-matched naïve animals, indicating that interhemispheric (IH) binding controlled by goal-directed, internal process. In S1 neurons, addition ipsilateral touch primarily facilitated contralateral, principal whisker response. facilitation for reward-associated lost on trials where failed respond. Taken together, these results reveal novel state-dependent logic underlying integration S1, are behavioral relevance.

Язык: Английский

Процитировано

0

Selective engagement of prefrontal VIP neurons in reversal learning DOI Creative Commons
Min Whan Jung, Jee Hyun Yi, Young Ju Yoon

и другие.

Research Square (Research Square), Год журнала: 2024, Номер unknown

Опубликована: Июнь 6, 2024

Abstract To gain insights into neural mechanisms enabling behavioral adaptations to complex and multidimensional environmental dynamics, we examined roles of VIP neurons in mouse medial prefrontal cortex (mPFC) probabilistic reversal learning. Behaviorally, manipulating neuronal activity left classical conditioning unaffected but severely impaired Physiologically, conditioned cue-associated responses changed abruptly after encountering an unexpected reward. They also conveyed strong reward prediction error signals during reversal, not before or after, unlike pyramidal which consistently throughout all phases. Furthermore, the signal’s persistence across trials correlated with learning duration. These results suggest that mPFC play crucial rapid learning, incremental cue-outcome association by monitoring significant deviations from ongoing contingency imposing error-correction adjustments. findings shed light on intricate cortical circuit dynamics underpinning flexibility complex, multifaceted environments.

Язык: Английский

Процитировано

0