Chemogenetic silencing reveals presynaptic Gi/o protein-mediated inhibition of developing hippocampal synchrony in vivo

Chemogenetic silencing reveals presynaptic G_i/o protein-mediated inhibition of developing hippocampal synchrony in vivo

Jürgen Graf*, Arash Samiee*, Tom Flossmann, Knut Holthoff, Knut Kirmse (2024)

iScience, Volume 27, Issue 10, 110997

https://doi.org/10.1016/j.isci.2024.110997

Recent advances in understanding how neuronal activity shapes developing brain circuits increasingly rely on G_i/o-dependent inhibitory chemogenetic tools (G_i-DREADDs). However, their mechanisms of action and efficacy in neurons with immature G_i/osignaling are elusive. Here, we express the G_i-DREADD hM4Di in glutamatergic telencephalic neurons and analyze its impact on CA1 pyramidal neurons in neonatal mice. Using acousto-optic two-photon Ca²⁺ imaging, we report that activation of hM4Di leads to a complete arrest of spontaneous synchrony in CA1 in vitro. We demonstrate that hM4Di does not cause somatic hyperpolarization or shunting but rather mediates presynaptic silencing of glutamatergic neurotransmission. In vivo, inhibition through hM4Di potently suppresses early sharp waves (eSPWs) and discontinuous oscillatory network activity in CA1 of head-fixed mice before eye opening. Our findings provide insights into the role of G_i/o signaling in synchronized activity in the neonatal hippocampus and bear relevance for applying chemogenetic silencing at early developmental stages.

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