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Results: 1 to 4 of 4

Publication Record


The role of the central melanocortin system in the regulation of food intake and energy homeostasis: lessons from mouse models.
Ellacott KL, Cone RD
(2006) Philos Trans R Soc Lond B Biol Sci 361: 1265-74
MeSH Terms: Animals, Energy Metabolism, Feeding Behavior, Homeostasis, Melanocortins, Melanocyte-Stimulating Hormones, Mice, Models, Animal
Show Abstract · Added December 10, 2013
A little more than a decade ago, the molecular basis of the lipostat was largely unknown. At that time, many laboratories were at work attempting to clone the genes encoding the obesity, diabetes, fatty, tubby and agouti loci, with the hope that identification of these obesity genes would help shed light on the process of energy homeostasis, appetite and energy expenditure. Characterization of obesity and diabetes elucidated the nature of the adipostatic hormone leptin and its receptor, respectively, while cloning of the agouti gene eventually led to the identification and characterization of one of the key neural systems upon which leptin acts to regulate intake and expenditure. In this review, we describe the neural circuitry known as the central melanocortin system and discuss the current understanding of its role in feeding and other processes involved in energy homeostasis.
0 Communities
2 Members
0 Resources
8 MeSH Terms
Leptin and inflammation-associated cachexia in chronic kidney disease.
Mak RH, Cheung W, Cone RD, Marks DL
(2006) Kidney Int 69: 794-7
MeSH Terms: Animals, Appetite, Cachexia, Humans, Inflammation, Inflammation Mediators, Kidney Failure, Chronic, Leptin, Melanocyte-Stimulating Hormones, Mice, Receptors, Cell Surface, Receptors, Leptin, Receptors, Melanocortin, Signal Transduction
Show Abstract · Added December 10, 2013
Leptin is an adipocyte-derived hormone that acts as a major regulator of food intake and energy homeostasis. It circulates both as a free and as a protein-bound entity. Leptin is released into the blood in proportion to the amount of body fat and exerts sustained inhibitory effects on food intake while increasing energy expenditure. The leptin receptor belongs to the class I cytokine receptor superfamily and possesses strong homology to the signal-transducing subunits of the IL-6 receptor. The hypothalamic melanocortin system, and specifically the melanocortin-4 receptor (MC-4R), is critical in mediating leptin's effect on appetite and metabolism. Serum leptin concentrations are elevated in patients with chronic kidney disease (CKD) and correlate with C-reactive protein levels suggesting that inflammation is an important factor that contributes to hyperleptinemia in CKD. Hyperleptinemia may be important in the pathogenesis of inflammation-associated cachexia in CKD. We showed that experimental uremic cachexia was attenuated in db/db mice, a model of leptin receptor deficiency. Nephrectomy in these animals did not result in any change in weight gain, body composition, resting metabolic rate, and efficiency of food consumption. Furthermore, experimental uremic cachexia could be ameliorated by blocking leptin signaling through the hypothalamic MC-4R. MC-4R knockout mice or mice administered the MC-4R and MC-3R antagonist, agouti-related peptide, resisted uremia-induced loss of lean body mass and maintained normal basal metabolic rates. Thus, melanocortin receptor antagonism may provide a novel therapeutic strategy for inflammation-associated cachexia in CKD.
0 Communities
1 Members
0 Resources
14 MeSH Terms
Interactions between gut peptides and the central melanocortin system in the regulation of energy homeostasis.
Ellacott KL, Halatchev IG, Cone RD
(2006) Peptides 27: 340-9
MeSH Terms: Animals, Cholecystokinin, Energy Metabolism, Gastrointestinal Tract, Ghrelin, Homeostasis, Humans, Melanocyte-Stimulating Hormones, Peptide Fragments, Peptide Hormones, Peptide YY, Peptides
Show Abstract · Added December 10, 2013
Genetic and pharmacological studies have shown that the central melanocortin system plays a critical role in the regulation of energy homeostasis. Animals and humans with defects in the central melanocortin system display a characteristic melanocortin obesity phenotype typified by increased adiposity, hyperphagia, metabolic defects and increased linear growth. In addition to interacting with long-term regulators of energy homeostasis such as leptin, more recent data suggest that the central melanocortin system also responds to gut-released peptides involved in mediating satiety. In this review, we discuss the interactions between these systems, with particular emphasis on cholecystokinin (CCK), ghrelin and PYY(3-36).
0 Communities
2 Members
0 Resources
12 MeSH Terms
Characterization of pro-ACTH/endorphin-derived peptides in rat hypothalamus.
Emeson RB, Eipper BA
(1986) J Neurosci 6: 837-49
MeSH Terms: Acetylation, Adrenocorticotropic Hormone, Amino Acid Sequence, Animals, Chromatography, Gel, Chromatography, High Pressure Liquid, Chromatography, Ion Exchange, Corticotropin-Like Intermediate Lobe Peptide, Endorphins, Hypothalamus, Isoelectric Focusing, Male, Melanocyte-Stimulating Hormones, Molecular Weight, Peptide Fragments, Pro-Opiomelanocortin, Rats, Rats, Inbred Strains, beta-Endorphin, beta-Lipotropin
Show Abstract · Added July 12, 2010
The proteolytic processing pattern of pro-ACTH/endorphin in rat hypothalamus is similar to the pattern in the pars intermedia; peptides the size of beta-endorphin, gamma-lipotropin (gamma-LPH), corticotropin-like intermediate lobe peptide (CLIP), alpha-melanotropin (gamma-MSH), joining peptide, and glycosylated gamma 3-MSH all represent predominant end products. Equimolar amounts of beta-endorphin-, alpha-MSH-, CLIP-, gamma-LPH-, and joining peptide-related immunoreactivity are found in hypothalamic extracts (approximately 3 pmol per hypothalamus). Although the proteolytic processing pattern in the hypothalamus is similar to that in the pars intermedia, a tissue-specific posttranslational processing pattern was detected. Ion-exchange analysis of beta-endorphin-sized immunoreactive material from hypothalamic extracts resolves three major forms, corresponding to beta-endorphin(1-31), beta-endorphin(1-27), and beta-endorphin(1-26). The alpha-N-acetylated forms of endorphin represent less than 10% of the total beta-endorphin immunoreactivity. Analyses of hypothalamic alpha-MSH-sized molecules with acetyl- and amide-directed alpha-MSH antisera suggest that hypothalamic alpha-MSH is fully amidated, but largely not alpha-N-acetylated. Fractionation by reverse-phase high-performance liquid chromatography (HPLC) confirms that greater than 85% of the alpha-MSH immunoreactivity corresponds to ACTH(1-13)NH2 or its sulfoxide, and less than 10% corresponds to alpha-MSH [alpha-N-acetyl-ACTH(1-13)NH2] or its sulfoxide. Isoelectric focusing demonstrates that 83-93% of hypothalamic CLIP is phosphorylated. Isoelectric focusing suggests that the majority of the hypothalamic gamma-LPH-sized immunoreactive material is indistinguishable from gamma-LPH synthesized by pituitary melanotropes. The minor extent of alpha-N-acetylation of alpha-MSH and beta-endorphin, the limited carboxyl-terminal proteolysis of beta-endorphin, and the extensive phosphorylation of CLIP represent major differences between the posttranslational processing patterns of pro-ACTH/endorphin in the hypothalamus and pars intermedia.
1 Communities
1 Members
0 Resources
20 MeSH Terms