Traditional sleep research has largely considered the cerebral cortex a passive recipient of sleep-inducing signals originating from deeper brain regions. The slow rhythms characteristic of deep sleep are visible in the cortex, but their initiation was previously attributed to subcortical areas.
A recent study published in Nature by Geoffrey Terral and Renata Batista-Brito from the Albert Einstein College of Medicine identified a specific population of cortical cells that can initiate these sleep rhythms. These cells, named Sst-Chodl neurons after two active genes, constitute approximately one percent of the cortex's inhibitory neurons.
The research demonstrated that activating these Sst-Chodl neurons in mice was sufficient to induce sleep in the animals. This indicates that the cortex is not merely observing sleep rhythms but can actively initiate them, a finding that alters previous understandings of sleep mechanisms.
Long-range inhibitory neurons marked by the activity of these genes have been known from studies in monkeys, but manipulating them proved difficult. Targeting a single gene would activate a broad range of different neurons, making specific manipulation challenging. The research team spent years developing a strategy to specifically label cells where both Sst and Chodl genes were active, enabling their targeted study.
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Researchers at Albert Einstein College of Medicine identified a population of cortical cells, called Sst-Chodl neurons, that can initiate sleep rhythms in the brain. This discovery challenges the long-held belief that sleep is primarily controlled by subcortical regions, suggesting the cortex plays a more active role in sleep induction.