Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/9400
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dc.contributor.authorGundlach, Andrew Len
dc.date.accessioned2015-05-15T22:28:54Z-
dc.date.available2015-05-15T22:28:54Z-
dc.date.issued2002-04-12en
dc.identifier.citationEuropean Journal of Pharmacology; 440(2-3): 255-68en
dc.identifier.govdoc12007540en
dc.identifier.otherPUBMEDen
dc.identifier.urihttp://ahro.austin.org.au/austinjspui/handle/1/9400en
dc.description.abstractScientific and commercial pharmacological interest in the role of galanin and galanin receptors in the regulation of food intake, energy balance, and obesity has waned recently, following initial enthusiasm during the 1980-1990s. It has been replaced by efforts to understand the role of newly discovered peptide systems such as the hypocretin/orexins, melanocortins and cocaine- and amphetamine-regulated transcript (CART) and their relationship to the important hormones, leptin and insulin. Thus, while numerous studies have revealed the ability of galanin to stimulate food intake via actions at sites within the hypothalamus, and shown reliable changes in hypothalamic galanin synthesis in response to food ingestion; findings including the lack of a 'body weight/obesity' phenotype in galanin transgenic mouse strains and a lack of agonists/antagonists for galanin receptor subtypes have probably served to reduce enthusiasm. However, as more is learnt about the general and galanin-related neurochemistry of brain pathways involved in feeding, metabolism and body weight control, the potential importance of galanin systems is again in focus. Studies of the newly discovered galanin family peptide, 'galanin-like peptide' (GALP), highlight the likely role of galanin peptides and receptors in the physiological coupling of body weight, adiposity and reproductive function. GALP is produced by a discrete population of neurons within the basomedial arcuate nucleus (and median eminence) that send projections to the anterior paraventricular nucleus and that make close contacts with leutinizing hormone-releasing hormone (LHRH) neurons in basal forebrain. Furthermore, GALP neurons express leptin receptors and respond to leptin treatment by increasing their expression of GALP mRNA. Centrally administered GALP activates LHRH-immunoreactive neurons and increases plasma LH levels. These findings suggest a direct stimulatory action of endogenous GALP on gonadotropin secretion via actions within the hypothalamus/basal forebrain, with leptin actions linking this system to body adipose levels.en
dc.language.isoenen
dc.subject.otherAmino Acid Sequenceen
dc.subject.otherBody Weight.physiologyen
dc.subject.otherEating.physiologyen
dc.subject.otherGalanin.genetics.pharmacology.physiologyen
dc.subject.otherGalanin-Like Peptideen
dc.subject.otherGene Expressionen
dc.subject.otherHumansen
dc.subject.otherHypothalamus.physiologyen
dc.subject.otherModels, Biologicalen
dc.subject.otherMolecular Sequence Dataen
dc.subject.otherMutationen
dc.subject.otherNerve Tissue Proteins.genetics.pharmacology.physiologyen
dc.subject.otherNeurons.drug effects.physiologyen
dc.subject.otherObesity.genetics.physiopathologyen
dc.subject.otherReceptors, Galaninen
dc.subject.otherReceptors, Neuropeptide.physiologyen
dc.subject.otherSequence Homology, Amino Aciden
dc.titleGalanin/GALP and galanin receptors: role in central control of feeding, body weight/obesity and reproduction?en
dc.typeJournal Articleen
dc.identifier.journaltitleEuropean Journal of Pharmacologyen
dc.identifier.affiliationHoward Florey Institute of Experimental Physiology and Medicine, and Department of Medicine, Austin and Repatriation Medical Centre, The University of Melbourne, Victoria, 3010, Australiaen
dc.description.pages255-68en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/12007540en
dc.type.austinJournal Articleen
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairetypeJournal Article-
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