| Literature DB >> 33888606 |
Mary Gazea1,2, Szabina Furdan3, Péter Sere3,4, Lukas Oesch2,3, Benedek Molnár3,4, Giuseppe Di Giovanni5,6, Lief E Fenno7, Charu Ramakrishnan8, Joanna Mattis7, Karl Deisseroth7,9, Susan M Dymecki10, Antoine R Adamantidis11,2, Magor L Lőrincz12,4,5.
Abstract
The lateral hypothalamus (LH), together with multiple neuromodulatory systems of the brain, such as the dorsal raphe nucleus (DR), is implicated in arousal, yet interactions between these systems are just beginning to be explored. Using a combination of viral tracing, circuit mapping, electrophysiological recordings from identified neurons, and combinatorial optogenetics in mice, we show that GABAergic neurons in the LH selectively inhibit GABAergic neurons in the DR, resulting in increased firing of a substantial fraction of its neurons that ultimately promotes arousal. These DRGABA neurons are wake active and project to multiple brain areas involved in the control of arousal, including the LH, where their specific activation potently influences local network activity leading to arousal from sleep. Our results show how mutual inhibitory projections between the LH and the DR promote wakefulness and suggest a complex arousal control by intimate interactions between long-range connections and local circuit dynamics.SIGNIFICANCE STATEMENT: Multiple brain systems including the lateral hypothalamus and raphe serotonergic system are involved in the regulation of the sleep/wake cycle, yet the interaction between these systems have remained elusive. Here we show that mutual disinhibition mediated by long range inhibitory projections between these brain areas can promote wakefulness. The main importance of this work relies in revealing the interaction between a brain area involved in autonomic regulation and another in controlling higher brain functions including reward, patience, mood and sensory coding.Entities:
Keywords: arousal; brain states; disinhibition; inhibition; neuromodulation; optogenetics
Mesh:
Year: 2021 PMID: 33888606 PMCID: PMC8260159 DOI: 10.1523/JNEUROSCI.2850-20.2021
Source DB: PubMed Journal: J Neurosci ISSN: 0270-6474 Impact factor: 6.167