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A genetically defined pontine nucleus essential for ingestion in mice
Selvee Sungeelee1, Caroline Mailhes-Hamon1, Zoubida Chettouh1
1Institut de Biologie de l'ENS, Inserm, Centre national de la recherche scientifique, École normale supérieure, Paris Sciences & Lettres Research University, Paris 75005, France.
Summary
Researchers identified a key brainstem nucleus, Sup5Phox2b, crucial for controlling biting and chewing during feeding. This discovery sheds light on the neural circuits governing oral motor patterns in mice.
Area of Science:
- Neuroscience
- Motor Control
- Feeding Behavior
Background:
- Feeding involves complex orofacial muscle coordination for biting and chewing.
- The precise neural circuits controlling these actions, particularly in the hindbrain reticular formation, remain poorly understood.
Purpose of the Study:
- To identify and characterize specific neuron groups in the brainstem involved in regulating orofacial motor patterns during feeding.
- To elucidate the role of the Phox2b-expressing nucleus in the supratrigeminal area (Sup5Phox2b) in feeding control.
Main Methods:
- Characterization of excitatory reticular interneurons expressing Phox2b in the supratrigeminal area.
- Investigation of neural inputs to the Sup5Phox2b nucleus from sensory and cortical regions.
- In vivo analysis of Sup5Phox2b neuronal activity during different feeding behaviors (lapping, biting, chewing).
- Optogenetic manipulation (activation/inhibition) of Sup5Phox2b neurons to assess their role in volitional feeding.
Main Results:
- Identified Sup5Phox2b as a premotor nucleus receiving sensory, motor cortex, and satiation-related inputs.
- Demonstrated that Sup5Phox2b activity differentially correlates with lapping, biting, and chewing.
- Showed that optogenetic activation or inhibition of Sup5Phox2b disrupts feeding sequences.
Conclusions:
- Sup5Phox2b is a critical, genetically and topologically defined subcortical node in the neural control of the oral phase of feeding.
- This nucleus plays an obligatory role in coordinating orofacial motor patterns essential for food intake in mice.

