Journal
EUROPEAN JOURNAL OF NEUROSCIENCE
Volume 37, Issue 6, Pages 891-900Publisher
WILEY-BLACKWELL
DOI: 10.1111/ejn.12084
Keywords
arousal; hypocretin; orexin; lateral hypothalamus; norepinephrine; sleep and wakefulness
Categories
Funding
- PHS [DA10681, DA00389]
- University of Wisconsin Graduate School
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Central norepinephrine exerts potent wake-promoting effects, in part through the actions of noradrenergic 1- and -receptors located in the medial septal and medial preoptic areas. The lateral hypothalamic area (LHA), including the lateral hypothalamus, perifornical area and adjacent dorsomedial hypothalamus, is implicated in the regulation of arousal and receives a substantial noradrenergic innervation. To date the functional significance of this innervation is unknown. The current studies examined the degree to which noradrenergic 1- and -receptor stimulation within the rat LHA modulates arousal. Specifically, these studies examined the wake-promoting effects of intra-tissue infusions (250nL) of the 1-receptor agonist phenylephrine (10, 20 and 40nmol) and the -receptor agonist isoproterenol (3, 10 and 30nmol) in rats. Results show that stimulation of LHA 1-receptors elicits robust and dose-dependent increases in waking. In contrast, -receptor stimulation within the LHA had relatively modest arousal-promoting actions. Nonetheless, combined 1- and -receptor stimulation elicited additive wake-promoting effects. Arousal-promoting hypocretin/orexin (HCRT)-synthesising neurons are located within the LHA. Therefore, additional immunohistochemical studies examined whether 1-receptor-dependent waking is associated with an activation of HCRT neurons as measured by Fos, the protein product of the immediateearly gene c-fos. Analyses indicate that although intra-LHA 1-receptor agonist infusion elicited a robust increase in Fos immunoreactivity (ir) in this region, this treatment did not activate HCRT neurons as measured by Fos-ir. Collectively, these observations indicate that noradrenergic 1-receptors within the LHA promote arousal via actions that are independent of HCRT neuronal activation.
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