Conceitos essenciais
Chronic heat exposure triggers negative emotional responses and hyperarousal in mice by inducing persistent activity changes in the neural pathway connecting the preoptic area (POA) to the posterior paraventricular thalamus (pPVT).
Estatísticas
Mice subjected to chronic heat exposure spent less time in the open arms of an elevated plus maze, indicating increased anxiety.
Chronic heat-exposed mice displayed reduced interest in exploring an unfamiliar mouse compared to an inanimate object, suggesting decreased sociability.
These mice also exhibited decreased latencies to attack and increased attack durations in a resident-intruder test, indicating elevated aggression.
Chronic heat exposure amplified the acoustic startle response in mice, suggesting hyperarousal.
Optogenetic activation of POA excitatory terminals in the pPVT induced aversion in a real-time place preference test.
This activation also led to pupil dilation, a physiological indicator of arousal.
Chronic optogenetic activation of the POA-pPVT pathway mimicked the behavioral effects of chronic heat exposure, inducing anxiety, decreased sociability, heightened aggression, and hyperarousal.
Optogenetic inhibition of POA recipient pPVT neurons during chronic heat exposure prevented the development of these behavioral changes.
Chronic heat exposure increased the frequency of miniature excitatory postsynaptic currents (mEPSCs) in pPVT neurons, indicating enhanced excitatory synaptic transmission.
pPVT neurons from chronic heat-exposed mice exhibited increased intrinsic excitability, characterized by a lower rheobase for action potential generation.
The POA-pPVT pathway in brain slices from chronic heat-exposed mice failed to exhibit long-term potentiation (LTP), suggesting that this pathway was already potentiated.