Abstract
Basic and clinical observations suggest that the caudal hypothalamus comprises a key node of the ascending arousal system, but the cell types underlying this are not fully understood. Here we report that glutamate-releasing neurons of the supramammillary region (SuM(vglut2)) produce sustained behavioral and EEG arousal when chemogenetically activated. This effect is nearly abolished following selective genetic disruption of glutamate release from SuM(vglut2) neurons. Inhibition of SuM(vglut2) neurons decreases and fragments wake, also suppressing theta and gamma frequency EEG activity. SuM(vglut2) neurons include a subpopulation containing both glutamate and GABA (SuM(vgat/vglut2)) and another also expressing nitric oxide synthase (SuM(Nos1/Vglut2)). Activation of SuM(vgat/vglut2) neurons produces minimal wake and optogenetic stimulation of SuM(vgat/vglut2) terminals elicits monosynaptic release of both glutamate and GABA onto dentate granule cells. Activation of SuM(Nos1/Vglut2) neurons potently drives wakefulness, whereas inhibition reduces REM sleep theta activity. These results identify SuM(vglut2) neurons as a key node of the wake-sleep regulatory system.