Crucial for survival, the central nervous system must reliably process sensory information over all stages of a hibernation bout to ensure homeostatic regulation is maintained and well-matched to dramatically altered behavioral states. Comparing neural responses in the nucleus tractus solitarius of rats and euthermic Syrian hamsters, we tested the hypothesis that hamster nucleus tractus solitarius neurons have adaptations sustaining signal processing while conserving energy. Using patch-clamp techniques, we classified second-order nucleus tractus solitarius neurons as rapid-onset or delayed-onset spiking phenotypes based on their spiking-onset to a depolarizing pulse (following a −80 mV prepulse). As temperature decreased from 33°C to 15°C, the excitability of all neurons decreased. However, hamster rapid-onset neurons had the highest spiking response and shortest action potential width at every temperature, while hamster delayed-onset neurons had the most negative resting membrane potential. Spontaneous excitatory post-synaptic current frequency in both phenotypes decreased as temperature decreased, yet tractus solitarius stimulation-evoked excitatory post-synaptic current amplitudes were greater in hamsters than in rats regardless of phenotype and temperature. Changes were significant (P<0.05), supporting our hypothesis by showing that, as temperature falls, rapid-onset neurons contribute more to signal processing but less to energy conservation than do delayed-onset neurons.