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Elevation of hilar mossy cell activity suppresses hippocampal excitability and avoidance behavior.
Wang, Kai-Yi; Wu, Jei-Wei; Cheng, Jen-Kun; Chen, Chun-Chung; Wong, Wai-Yi; Averkin, Robert G; Tamás, Gábor; Nakazawa, Kazu; Lien, Cheng-Chang.
Afiliação
  • Wang KY; Institute of Neuroscience, National Yang Ming Chiao Tung University, Taipei 11221, Taiwan.
  • Wu JW; Institute of Neuroscience, National Yang Ming Chiao Tung University, Taipei 11221, Taiwan.
  • Cheng JK; Department of Medicine, Mackay Medical College, New Taipei 252, Taiwan; Department of Anesthesiology, Mackay Memorial Hospital, Taipei 104, Taiwan.
  • Chen CC; Institute of Physics, Academia Sinica, Taipei 115, Taiwan.
  • Wong WY; Institute of Neuroscience, National Yang Ming Chiao Tung University, Taipei 11221, Taiwan.
  • Averkin RG; ELKH-SZTE Research Group for Cortical Microcircuits, Department of Physiology, Anatomy and Neuroscience, University of Szeged, Közép fasor 52, Szeged 6726, Hungary.
  • Tamás G; ELKH-SZTE Research Group for Cortical Microcircuits, Department of Physiology, Anatomy and Neuroscience, University of Szeged, Közép fasor 52, Szeged 6726, Hungary.
  • Nakazawa K; Department of Neuroscience, Southern Research, Birmingham, AL 35205, USA; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Lien CC; Institute of Neuroscience, National Yang Ming Chiao Tung University, Taipei 11221, Taiwan; Brain Research Center, National Yang Ming Chiao Tung University, Taipei 11221, Taiwan. Electronic address: cclien@nycu.edu.tw.
Cell Rep ; 36(11): 109702, 2021 09 14.
Article em En | MEDLINE | ID: mdl-34525354
ABSTRACT
Modulation of hippocampal dentate gyrus (DG) excitability regulates anxiety. In the DG, glutamatergic mossy cells (MCs) receive the excitatory drive from principal granule cells (GCs) and mediate the feedback excitation and inhibition of GCs. However, the circuit mechanism by which MCs regulate anxiety-related information routing through hippocampal circuits remains unclear. Moreover, the correlation between MC activity and anxiety states is unclear. In this study, we first demonstrate, by means of calcium fiber photometry, that MC activity in the ventral hippocampus (vHPC) of mice increases while they explore anxiogenic environments. Next, juxtacellular recordings reveal that optogenetic activation of MCs preferentially recruits GABAergic neurons, thereby suppressing GCs and ventral CA1 neurons. Finally, chemogenetic excitation of MCs in the vHPC reduces avoidance behaviors in both healthy and anxious mice. These results not only indicate an anxiolytic role of MCs but also suggest that MCs may be a potential therapeutic target for anxiety disorders.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Comportamento Animal / Fibras Musgosas Hipocampais / Hipocampo Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Comportamento Animal / Fibras Musgosas Hipocampais / Hipocampo Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article