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Journal ArticleDOI

Post-prandial decrease of circulating human ghrelin levels.

TLDR
Ghrelin appears to be one possible candidate to provide feedback signaling between nutrient intake, gastric motor function and the central nervous system.
Abstract
Ghrelin, an endogenous ligand of the GH secretagogue-receptor, has recently been shown to stimulate GH secretion and to have orexigenic and adipogenic effects in rodents, but little is known about its regulation and biological function in humans. Gastric motor function is under control of the central nervous system; however, the afferent and efferent loops of this feedback control mechanism remain to be elucidated. In the study presented here we investigated the effect of nutrient intake on circulating human ghrelin levels, and a possible association between ghrelin levels and gastric emptying. Ten healthy volunteers received a standard meal after an overnight fast. Food intake significantly decreased plasma ghrelin levels from 248.5±15.0 to 179.5±17.9 fmol/ml (120 min after meal, p=0.047). Gastric emptying half-time (non-invasive 13C-octanoic acid breath test) was correlated with fasting plasma ghrelin levels (r=0.74, p=0.0013). Ghrelin appears to be one possible candidate to provide feedback signaling between nutrient intake, gastric motor function and the central nervous system.

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Journal ArticleDOI

Ghrelin: Structure and Function

TL;DR: The discovery of ghrelin indicates that the release of GH from the pituitary might be regulated not only by hypothalamic GH-releasing hormone, but also by gh Relin derived from the stomach, which plays important roles for maintaining GH release and energy homeostasis in vertebrates.
Journal ArticleDOI

Anatomy and regulation of the central melanocortin system.

TL;DR: Given that the central melanocortin system is an active target for development of drugs for the treatment of obesity, diabetes and cachexia, it is important to understand the system in its full complexity, including the likelihood that the system also regulates the cardiovascular and reproductive systems.
Journal ArticleDOI

Biological, physiological, pathophysiological, and pharmacological aspects of ghrelin.

TL;DR: Ghrelin is considered a gastrointestinal peptide contributing to the regulation of diverse functions of the gut-brain axis and there is indeed a possibility that ghrelin analogs, acting as either agonists or antagonists, might have clinical impact.
Journal ArticleDOI

The role of leptin and ghrelin in the regulation of food intake and body weight in humans: a review.

TL;DR: A review of the role of leptin and ghrelin in food intake and body weight in humans and their mechanism of action is presented in this article, where possible abnormalities in the leptin and Ghrelin systems that may contribute to the development of obesity are discussed.
References
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Journal ArticleDOI

Ghrelin is a growth-hormone-releasing acylated peptide from stomach.

TL;DR: The occurrence of ghrelin in both rat and human indicates that GH release from the pituitary may be regulated not only by hypothalamic GHRH, but also by ghrelIn, a peptide specifically releases GH both in vivo and in vitro.
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Ghrelin induces adiposity in rodents.

TL;DR: It is proposed that ghrelin, in addition to its role in regulating GH secretion, signals the hypothalamus when an increase in metabolic efficiency is necessary, suggesting an involvement in regulation of energy balance.
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Ghrelin is an appetite-stimulatory signal from stomach with structural resemblance to motilin.

TL;DR: Ghrelin, which is negatively regulated by leptin and IL-1 beta, is secreted by the stomach and increases arcuate NPY expression, which in turn acts through Y(1) receptors to increase food intake and decrease energy expenditure.
Journal ArticleDOI

Ghrelin stimulates gastric acid secretion and motility in rats.

TL;DR: Intravenous administrations of rat ghrelin at 0.8 to 20 microgram/kg dose-dependently increased not only gastric acid secretion measured by a lumen-perfused method, but also gastric motility measured byA miniature balloon method suggest that gh Relin may play a physiological role in the vagal control of gastric function in rats.
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