4.7 Article

Bidirectional Communication between the Pontine Nucleus Incertus and the Medial Septum Is Carried Out by Electrophysiologically-Distinct Neuronal Populations

Journal

JOURNAL OF NEUROSCIENCE
Volume 42, Issue 11, Pages 2234-2252

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.0230-21.2022

Keywords

delta waves; electrophysiology; medial septum; nucleus incertus; theta rhythm

Categories

Funding

  1. Polish National Science Center [UMO-2019/33/B/NZ4/03127, UMO-2018/30/E/NZ4/00687]
  2. doctoral scholarship Etiuda VI [2018/28/T/NZ4/00382]
  3. doctoral scholarship Etiuda VIII [2020/36/T/NZ4/00341, 14 2017/27/N/NZ4/00785]
  4. Institute of Zoology and Biomedical Research, Jagiellonian University
  5. Excellence Initiative-Research University at the Faculty of Biology of the Jagiellonian University in Krakow, Poland

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Theta oscillations play a key role in memory formation, sensorimotor integration, and control of locomotion and behavioral states. This study investigated the generation and synchronization of theta oscillations in the brain, particularly focusing on the interactions between brain nuclei and the medial septum (MS). The researchers discovered distinct populations of neurons in the pontine nucleus incertus (NI) that fire action potentials in different manners and have different connections with the MS. These findings provide insights into the mechanisms of theta rhythm generation and transmission in the brain.
Theta oscillations are key brain rhythm involved in memory formation, sensorimotor integration, and control of locomotion and behavioral states. Generation and spatiotemporal synchronization of theta oscillations rely on interactions between brain nuclei forming a large neural network, which includes pontine nucleus incertus (NI). Here we identified distinct populations of NI neurons, based on the relationship of their firing to hippocampal waves, with a special focus on theta oscillations, and the direction and type of interaction with the medial septum (MS) in male, urethane-anesthetized rats. By recording NI neuronal firing and hippocampal LFP, we described NI neurons that fire action potentials in a theta phase-independent or theta phase-locked and delta wave-independent or delta wave-locked manner. Among hippocampal activity-independent NI neurons, irregular, slow-firing, and regular, fast-firing cells were observed, while hippocampal oscillation-/wave-locked NI neurons were of a bursting or nonbursting type. By projection-specific optotagging, we revealed that only fast-firing theta phase-independent NI neurons innervate the MS, rarely receiving feedback information. In contrast, the majority of theta-bursting NI neurons were inhibited by MS stimulation, and this effect was mediated by direct GABAergic input. Described NI neuronal populations differ in reciprocal connections with the septohippocampal system, plausibly forming separate neuronal loops. Our results suggest that theta phase-independent NI neurons participate in theta rhythm generation through direct innervation of the MS, while theta-bursting NI neurons further transmit the rhythmic signal received from the MS to stabilize and/or strengthen rhythmic activity in other structures.

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