TY - JOUR
T1 - Loss of mGlu5 receptors in somatostatin-expressing neurons alters negative emotional states
AU - Ramos-Prats, Arnau
AU - Matulewicz, Pawel
AU - Edenhofer, Marie Luise
AU - Wang, Kai Yi
AU - Yeh, Chia Wei
AU - Fajardo-Serrano, Ana
AU - Kress, Michaela
AU - Kummer, Kai
AU - Lien, Cheng Chang
AU - Ferraguti, Francesco
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/9
Y1 - 2024/9
N2 - Subtype 5 metabotropic glutamate receptors (mGlu5) are known to play an important role in regulating cognitive, social and valence systems. However, it remains largely unknown at which circuits and neuronal types mGlu5 act to influence these behavioral domains. Altered tissue- or cell-specific expression or function of mGlu5 has been proposed to contribute to the exacerbation of neuropsychiatric disorders. Here, we examined how these receptors regulate the activity of somatostatin-expressing (SST+) neurons, as well as their influence on behavior and brain rhythmic activity. Loss of mGlu5 in SST+ neurons elicited excitatory synaptic dysfunction in a region and sex-specific manner together with a range of emotional imbalances including diminished social novelty preference, reduced anxiety-like behavior and decreased freezing during retrieval of fear memories. In addition, the absence of mGlu5 in SST+ neurons during fear processing impaired theta frequency oscillatory activity in the medial prefrontal cortex and ventral hippocampus. These findings reveal a critical role of mGlu5 in controlling SST+ neurons excitability necessary for regulating negative emotional states.
AB - Subtype 5 metabotropic glutamate receptors (mGlu5) are known to play an important role in regulating cognitive, social and valence systems. However, it remains largely unknown at which circuits and neuronal types mGlu5 act to influence these behavioral domains. Altered tissue- or cell-specific expression or function of mGlu5 has been proposed to contribute to the exacerbation of neuropsychiatric disorders. Here, we examined how these receptors regulate the activity of somatostatin-expressing (SST+) neurons, as well as their influence on behavior and brain rhythmic activity. Loss of mGlu5 in SST+ neurons elicited excitatory synaptic dysfunction in a region and sex-specific manner together with a range of emotional imbalances including diminished social novelty preference, reduced anxiety-like behavior and decreased freezing during retrieval of fear memories. In addition, the absence of mGlu5 in SST+ neurons during fear processing impaired theta frequency oscillatory activity in the medial prefrontal cortex and ventral hippocampus. These findings reveal a critical role of mGlu5 in controlling SST+ neurons excitability necessary for regulating negative emotional states.
UR - http://www.scopus.com/inward/record.url?scp=85189646883&partnerID=8YFLogxK
U2 - 10.1038/s41380-024-02541-5
DO - 10.1038/s41380-024-02541-5
M3 - Article
AN - SCOPUS:85189646883
SN - 1359-4184
VL - 29
SP - 2774
EP - 2786
JO - Molecular Psychiatry
JF - Molecular Psychiatry
IS - 9
ER -