The focus of the present review is to reconsider the role of endogenous nor
epinephrine (NE) in brain, specifically within the hypothalamic paraventric
ular nucleus (PVN), with regard to its potential role in eliciting eating o
r satiety. The PVN is innervated by NE fibers and is a site at which infusi
on of exogenous NE elicits eating at low doses. Two subtypes of alpha -adre
nergic receptors within the PVN exert antagonistic actions on eating in the
rat:activation of PVN alpha (2)-adrenoceptors increases eating, whereas ac
tivation of PVN alpha (1)-adrenoceptors suppresses eating. Pharmacologic ma
nipulations that elevate NE can increase or decrease food intake; depending
on the site and type of NE manipulation. Certain antiobesity drugs may act
to reduce eating via release of NE and subsequent activation of alpha (1)-
adrenoceptors. The PVN exhibits a reliable rhythm in the secretion of endog
enous NE over the dark-and-light cycle, and this rhythm may interact with c
hanges in numbers of PVN alpha (1)- and alpha (2)-adrenoceptors to modulate
eating during the dark-and-light cycle. Push-and-pull and microdialysis st
udies indicate that NE secretion is strongly associated with eating, partic
ularly at the start of the dark phase. The present review considers potenti
al interactions of NE with substances such as leptin and neuropeptide Y tha
t alter eating. Nutrition 2000; 16:837-842. (C) Elsevier Science Inc. 2000.