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Systemic Administration of Orexin a Loaded Liposomes Potentiates Nucleus Accumbens Shell Dopamine Release by Sucrose Feeding

Bibliographic Data

ID15519212
AuthorsFrancesco Lai (University of Cagliari), Flavia Cucca (University of Cagliari), Roberto Frau (0000-0002-5922-2404, University of Cagliari), Francesco Corrias (0000-0002-1324-7681, University of Cagliari), Michele Schlich (0000-0002-7214-9045, University of Cagliari), Pierluigi Caboni (0000-0003-2448-3767, University of Cagliari), Anna Maria Fadda (0000-0001-9848-0556, University of Cagliari), Valentina Bassareo (0000-0001-9439-6090, University of Cagliari, corresponding author)
Year2018
Volume9
Pages640-640
Publication date2018-12-03
Open AccessYes
TypeARTICLE
VenueFrontiers in Psychiatry (JOURNAL)
Journal identifiersISSN: 1664-0640 • E-ISSN: 1664-0640
PublisherFrontiers Media (PUBLISHER • CH)
DOI10.3389/fpsyt.2018.00640
PMID30559683
OpenAlexW2902749596
LanguageEN
References cited65

Orexin neurons originate in the lateral and dorsomedial hypothalamus and perifornical area and produce two different neuropeptides: orexin A (OxA) and orexin B (OxB), which activate OxR1 and OxR2 receptors. In the lateral hypothalamus (LH) orexin neurons are involved in behavior motivated by natural rewards such as palatable food (sugar, high-fat food) and it has been demonstrated similarly that the orexin signaling in the ventral tegmental area (VTA) is implicated in the intake of high-fat food. The VTA is an important area involved in reward processing. Given the involvement of nucleus accumbens (NAc) shell dopamine (DA) in motivation for food, we intended to investigate the effect of OxA on the basal and feeding-activated DA transmission in the NAc shell. OxA is a large peptide and does not cross the blood-brain barrier and for this reason was loaded on two kinds of liposomes: anti-transferrin-monoclonal antibodies (OX26-mAb) and lactoferrin-modified stealth liposomes. The effect of IV administration of both OxA liposomes on NAc shell DA was studied by microdialysis in freely moving rats. OxA, administered using both kinds of liposomes, produced a delayed and transitory increase in dialysate DA in the NAc shell, strongly and lastingly potentiated the increase in dialysate DA elicited by sucrose pellet consumption and increased the number of eaten pellets. These effects of OxA on DA transmission and feeding were prevented by the OxR1 antagonist SB 334867. Hence, OxA acting on VTA OxR1 can facilitate sucrose-stimulated NAc shell DA transmission directly by increasing the basal activity of VTA DA neurons that send their projections to the NAc shell

Dopamine · Dopaminergic · Hypothalamus · Lateral hypothalamus · Microdialysis · Neuropeptide · Nucleus accumbens · Orexin · Orexin-A · Receptor · Ventral tegmental area · Chemistry · Medicine · Regulation of Appetite and Obesity · Sleep and related disorders · Sleep and Wakefulness Research · Endocrinology · Internal Medicine · Pharmacology

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Highly citedNo

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