Enhanced nicotinic acetylcholine receptor-mediated [ 3H]norepinephrine release from neonatal rat hypothalamus

• Published in: Neuropharmacology Vol. 50; no. 1; pp. 81 - 88
• Main Authors: O'Leary, K.T., Leslie, F.M.
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 2006
• Subjects: Aconitine - analogs & derivatives; Aconitine - pharmacology; Animals; Animals, Newborn - metabolism; Benzylamines - pharmacology; Catecholamine; Dose-Response Relationship, Drug; Hypothalamus - cytology; Hypothalamus - metabolism; In Vitro Techniques; Locus coeruleus; Male; Neurons, Afferent - drug effects; Neurons, Afferent - metabolism; Neurotransmitter Agents - metabolism; Neurotransmitter release; Nicotine; Nicotinic Antagonists - pharmacology; Norepinephrine - metabolism; Ontogeny; Rats; Rats, Sprague-Dawley; Receptors, Nicotinic - drug effects; Receptors, Nicotinic - metabolism; Tubocurarine - pharmacology; Neurotransmitter release; Ontogeny; Catecholamine; Locus coeruleus; Nicotine
• ISSN: 0028-3908; 1873-7064
• DOI: 10.1016/j.neuropharm.2005.08.013

Nicotinic acetylcholine receptor (nAChR)-evoked release of norepinephrine (NE) has been demonstrated in a number of brain regions that receive sole noradrenergic innervation from the locus coeruleus (LC). Many of these structures display enhanced nicotine-stimulated NE release in the neonate. We have examined the hypothalamus in order to determine if this region, which receives NE projections from both the LC and medullary catecholaminergic nuclei, also demonstrates maturational changes in nAChR-mediated NE release. Quantification of radiolabeled-NE release from rat hypothalamus slices by a maximally effective dose of nicotine revealed a peak response during the first postnatal week. This was followed by a decrease at postnatal day (P) 14, and a second peak at P21. Thereafter, release was equivalent to that observed at P14. Comparison of the pharmacological properties of nAChRs mediating NE release in neonatal (P7) and mature hypothalamus suggested involvement of different nAChR subtypes at the two ages. Using the selective toxin, DSP-4, nAChR-mediated NE release in the neonatal hypothalamus was shown to be from LC terminals. Our findings demonstrate an early sensitivity of hypothalamic LC terminals to nAChR regulation that may be associated with development of systems controlling critical homeostatic functions such as stress, feeding and cardiovascular regulation.