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Somatostatin-Positive Neurons in the Rostral Zona Incerta Modulate Innate Fear-Induced Defensive Response in Mice

Shan Lin; Meng-Yue Zhu; Meng-Yu Tang; Mi Wang; Xiao-Dan Yu; Yi Zhu; Shi-Ze Xie; Dan Yang; Jiadong Chen; Xiao-Ming Li
Neuroscience Bulletin · Vol. 39, Issue 2 · pp. 245-260 · 2023

Abstract

Defensive behaviors induced by innate fear or Pavlovian fear conditioning are crucial for animals to avoid threats and ensure survival. The zona incerta (ZI) has been demonstrated to play important roles in fear learning and fear memory, as well as modulating auditory-induced innate defensive behavior. However, whether the neuronal subtypes in the ZI and specific circuits can mediate the innate fear response is largely unknown. Here, we found that somatostatin (SST)-positive neurons in the rostral ZI of mice were activated by a visual innate fear stimulus. Optogenetic inhibition of SST-positive neurons in the rostral ZI resulted in reduced flight responses to an overhead looming stimulus. Optogenetic activation of SST-positive neurons in the rostral ZI induced fear-like defensive behavior including increased immobility and bradycardia. In addition, we demonstrated that manipulation of the GABAergic projections from SST-positive neurons in the rostral ZI to the downstream nucleus reuniens (Re) mediated fear-like defensive behavior. Retrograde trans-synaptic tracing also revealed looming stimulus-activated neurons in the superior colliculus (SC) that projected to the Re-projecting SST-positive neurons in the rostral ZI (SC-ZIr SST -Re pathway). Together, our study elucidates the function of SST-positive neurons in the rostral ZI and the SC-ZIr SST -Re tri-synaptic circuit in mediating the innate fear response.

Bibliographic Information

JournalNeuroscience Bulletin
PublisherSpringer
Publication Date2023-02-01
Publication Year2023
Volume39
Issue2
Pages245-260
Document TypeJournal Article
Print ISSN1673-7067
eISSN1995-8218
DOI10.1007/s12264-022-00958-y

Access Information

NARA Access Coverage2007-01-01~Current
Journal Homepagehttps://www.springer.com/journal/12264
Publisher PageOpen Publisher Page
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