Cholecystokinin neurons in the spinal trigeminal nucleus interpolaris regulate mechanically evoked predatory hunting in male mice

Predatory hunting plays a critical role in animal survival. Motion-related vibrissal somatosensory signaling is essential for prey detection and hunting in mice. However, little is known about the neural circuits that convert vibrissal somatosensory cues to trigger predatory hunting. Here, we report that mechanical force onto the vibrissal area of the male mice is a key stimulus for predatory hunting. Mechanically evoked predatory hunting was abrogated by the chemogenetic inactivation of cholecystokinin-positive (Cck<sup>+</sup>) neurons in the spinal trigeminal nucleus interpolaris (Sp5I). The Cck<sup>+</sup> Sp5I neurons responded to the intensity of mechanical stimulus and sent neural signals to the superior colliculus that were relevant to stereotypical predatory hunting motor actions. Synaptic inactivation of the projections from Cck<sup>+</sup> Sp5I neurons to the superior colliculus impaired mechanically evoked predatory attacks. Together, these data reveal a spinal trigeminal nucleus neural circuit that is specifically engaged in translating vibrissal somatosensory cues to provoke predatory hunting.

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Publication Details

Journal
Nature Communications
Published
2025-03-14
DOI
https://doi.org/10.1038/s41467-025-57771-0
Primary Topic
Neurobiology and Insect Physiology Research
Type
article
Field-Weighted Citation Impact
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article

Cholecystokinin neurons in the spinal trigeminal nucleus interpolaris regulate mechanically evoked predatory hunting in male mice

Bo Yang, Qingzhuo Cui, Peng Cao, Huating Gu et al.
Nature Communications
Neurobiology and Insect Physiology Research
article

Cholecystokinin neurons in the spinal trigeminal nucleus interpolaris regulate mechanically evoked predatory hunting in male mice

Bo Yang, Qingzhuo Cui, Peng Cao, Huating Gu, Rong Zheng, Hui Liu, Fan Zhang, Li Zhang, Yaning Li, Tianyun Zhang, Dandan Geng, Zijie Zhao
article en

Abstract

Predatory hunting plays a critical role in animal survival. Motion-related vibrissal somatosensory signaling is essential for prey detection and hunting in mice. However, little is known about the neural circuits that convert vibrissal somatosensory cues to trigger predatory hunting. Here, we report that mechanical force onto the vibrissal area of the male mice is a key stimulus for predatory hunting. Mechanically evoked predatory hunting was abrogated by the chemogenetic inactivation of cholecystokinin-positive (Cck<sup>+</sup>) neurons in the spinal trigeminal nucleus interpolaris (Sp5I). The Cck<sup>+</sup> Sp5I neurons responded to the intensity of mechanical stimulus and sent neural signals to the superior colliculus that were relevant to stereotypical predatory hunting motor actions. Synaptic inactivation of the projections from Cck<sup>+</sup> Sp5I neurons to the superior colliculus impaired mechanically evoked predatory attacks. Together, these data reveal a spinal trigeminal nucleus neural circuit that is specifically engaged in translating vibrissal somatosensory cues to provoke predatory hunting.

Nature CommunicationsVol. 16(1)
Hebei Medical University (CN), Ministry of Education of the People's Republic of China (CN), National Institute of Biological Sciences, Beijing (CN), Hospital of Hebei Province (CN), Tsinghua University (CN)
Openalex Percentile: Top 94%
Neurobiology and Insect Physiology Research
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