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Logas, K.

Publications and source records attributed to Logas, K..

2 recordsLinked to original sources

Paraventricular thalamus gates hippocampal coding of salient experiences.

Adaptive behavior requires neural circuits that encode salient stimuli to guide approach and avoidance. The hippocampal ventral subiculum (vSub) encodes information related to avoidance and reward seeking, yet how upstream inputs shape its representations of salient appetitive and aversive events remains unclear. Here, we show that a projection from the anterior paraventricular thalamus (PVT) to vSub carries an aversive-state signal that biases vSub representations toward threat-related information. In anxiety-provoking environments, anterior PVT to vSub activity is associated with avoidance behavior and enhanced vSub discrimination of threat and safety. During associative learning, this circuit preferentially promotes vSub responses to threat-predictive cues and aversive outcomes while constraining representations of rewarding stimuli. These findings refine canonical limbic circuit models by identifying a direct thalamic influence over hippocampal coding of rewarding versus aversive stimuli and the approach-avoidance behaviors they guide.

neuroscience↗

vCA1 SST neurons represent avoidance states that guide anxiety-related behavioral choices

In uncertain, threatening environments, rapid and flexible behavioral decisions are essential for survival. The ventral CA1 region of the hippocampus encodes threatening contexts and can regulate avoidance-related behaviors. While activity patterns in excitatory neurons of vCA1 have been well characterized, the contributions of specific interneuron subtypes to avoidance decisions in threatening situations remain to be fully elucidated. Here, we show that somatostatin expressing (SST) interneurons in vCA1 are selectively recruited during avoidance behavior and play a causal role in shaping behavioral responses in aversive spaces. We find that vCA1 SST interneurons ramp their activity in anticipation of, and during, avoidance. This contrasted with parvalbumin (PV) and vasoactive intestinal peptide (VIP) interneurons, which are preferentially active during exploratory approach behaviors. Unlike other classes of vCA1 interneurons, SST neuron activity more reliably represented the animals intention to avoid rather than its spatial position. Moreover, optogenetic silencing of SST interneurons reduced the efficiency of approach-avoidance decisions. These findings identify vCA1 SST interneurons as key regulators of threat assessment, revealing a cell-type-specific mechanism by which vCA1 microcircuits govern avoidance behaviors. This work provides a new framework for understanding hippocampal control of avoidance behavior and highlights SST-expressing interneurons as key contributors to anxiety-related behaviors.

neuroscience↗