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Scheunemann, L.

Publications and source records attributed to Scheunemann, L..

2 recordsLinked to original sources

A state-dependent neural circuit resolves approach-avoidance conflicts

To survive, animals must balance opportunity and risk, yet how internal motivational state biases this trade-off remains poorly understood. Here we show that hunger gates nociceptive avoidance in Drosophila to enable food approach under conflict. Using a behavioural assay in which flies must cross an electric shock barrier to reach food, we find that starvation promotes shock tolerance only when food-related olfactory cues are present. This state- and context-dependent behavioural shift is mediated by a defined neuromodulatory circuit. Leucokinin neurons encode hunger and convey this information to PV5K1 lateral horn output neurons, which integrate internal state signals with food odour cues and suppress shock-responsive FB2B neurons in the ventral fan-shaped body. Accordingly, electric shock-evoked activity in FB2B neurons is suppressed in starved flies exposed to food cues. These findings identify a circuit mechanism by which motivational state gates aversive processing to bias action selection towards goal-directed behaviour. TeaserHunger enables flies to suppress nociceptive avoidance when food cues signal reward availability via a defined neuromodulatory circuit.

neuroscience↗

Mating proximity blinds threat perception.

Romantic engagement can bias sensory perception. This love blindness reflects a common behavioral principle across organisms: favoring pursuit of a coveted reward over potential risks. In the case of animal courtship, such sensory biases may support reproductive success but can also expose individuals to danger, such as predation. How do neural networks balance the trade-off between risk and reward? Here, we discover a dopamine-governed filter mechanism in male Drosophila that reduces threat perception as courtship progresses. We show that during early courtship stages, threat-activated visual neurons inhibit central courtship nodes via specific serotonergic neurons. This serotonergic inhibition prompts flies to abort courtship when they see imminent danger. However, as flies advance in the courtship process, the dopaminergic filter system reduces visual threat responses, shifting the balance from survival to mating. By recording neural activity from males as they approach mating, we demonstrate that progress in courtship is registered as dopaminergic activity levels ramping up. This dopamine signaling inhibits the visual threat detection pathway via Dop2R receptors, allowing male flies to focus on courtship when they are close to copulation. Thus, dopamine signaling biases sensory perception based on perceived goal proximity, in order to prioritize between competing behaviors.

neuroscience↗