Coordinatore | THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE
Organization address
address: The Old Schools, Trinity Lane contact info |
Nazionalità Coordinatore | United Kingdom [UK] |
Sito del progetto | http://www.eurochip-obesity.com |
Totale costo | 3˙854˙510 € |
EC contributo | 2˙999˙996 € |
Programma | FP7-HEALTH
Specific Programme "Cooperation": Health |
Code Call | FP7-HEALTH-2009-single-stage |
Funding Scheme | CP-FP |
Anno di inizio | 2009 |
Periodo (anno-mese-giorno) | 2009-10-01 - 2013-09-30 |
# | ||||
---|---|---|---|---|
1 |
THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE
Organization address
address: The Old Schools, Trinity Lane contact info |
UK (CAMBRIDGE) | coordinator | 546˙666.11 |
2 |
KLINIKUM DER UNIVERSITAET ZU KOELN
Organization address
address: Kerpener Strasse 62 contact info |
DE (KOELN) | participant | 387˙640.00 |
3 |
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM)
Organization address
address: 101 Rue de Tolbiac contact info |
FR (PARIS) | participant | 387˙560.00 |
4 |
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE
Organization address
address: Rue Michel -Ange 3 contact info |
FR (PARIS) | participant | 387˙440.00 |
5 |
IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE
Organization address
address: SOUTH KENSINGTON CAMPUS EXHIBITION ROAD contact info |
UK (LONDON) | participant | 387˙440.00 |
6 |
GOETEBORGS UNIVERSITET
Organization address
address: VASAPARKEN contact info |
SE (GOETEBORG) | participant | 387˙400.00 |
7 |
HELMHOLTZ ZENTRUM MUENCHEN DEUTSCHES FORSCHUNGSZENTRUM FUER GESUNDHEIT UND UMWELT GMBH
Organization address
address: Ingolstaedter Landstrasse 1 contact info |
DE (MUENCHEN) | participant | 215˙215.75 |
8 |
DEUTSCHES INSTITUT FUER ERNAEHRUNGSFORSCHUNG POTSDAM REHBRUECKE
Organization address
address: Arthur-Scheunert-Allee 114-116 contact info |
DE (NUTHETAL) | participant | 172˙289.14 |
9 |
EUROQUALITY SARL
Organization address
address: Rue de l'Isly 8 contact info |
FR (PARIS) | participant | 128˙345.00 |
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'The past decade has seen tremendous progress in our understanding of homeostatic regulators controlling energy balance. Insights from human and murine genetics have illuminated multiples pathways within the hypothalamus, brainstem and higher brain regions that play a key role in the control of food intake, whilst physiological studies focusing on the gastrointestinal tract have revealed a panoply of hormones that are secreted in response to or in anticipation of food intake and act centrally to regulate appetite. EurOCHIP brings together world leaders specializing in both areas in order to explore the interaction between the periphery and the brain in the control of energy homeostasis. Our programme of research will comprise four interdependent work-packages: i) characterising the interaction of gastrointestinal hormones with the hypothalamus and brainstem, with the aim of identifying novel molecules and pathways that mediate food intake; ii) using imaging techniques and behavioural phenotyping to explore the response of brain areas involved in higher cognitive and affective functions to these gastrointestinal hormones; iii) harnessing the power of human genetics to determine the role of sequence variation in and around newly identified candidate genes in appetitive behaviour and response to dietary interventions, focusing in particular on childhood obesity and iv) determining the effects of specific dietary interventions on gastrointestinal hormone secretion and using pharmacological studies in humans to mimic the hormonal milieu seen after a meal or bariatric surgery.'
A European study proved that understanding the physiology of food intake and body-weight control can provide the answer to obesity.
Obesity represents one of the main health challenges of the 21st century. Its high incidence and adverse impact on health poses a heavy socioeconomic burden in most European countries. Current treatment modalities are limited and bariatric surgery is often the only option.
Energy homeostasis is a complex process that critically depends on the regulated communication between the gastrointestinal tract and the brain. Specific signals inform the brain about nutrient stores as well as the ingestive status, thereby influencing meal initiation and termination.
In this context, scientists on the EU- funded 'European obesity consortium studying the hypothalamus and its interaction with peripheral organs' (http://www.eurochip-obesity.com/ (EUROCHIP)) project proposed that devising new treatments for obesity requires in-depth investigation of the signals from the gut to the brain.
Researchers performed extensive gene expression analysis to identify the effector systems in the hypothalamus and brainstem, which are regulated by gut peptides such as ghrelin.
They discovered that chronic ghrelin administration increased food intake and that a high fat diet rendered certain parts of the brain resistant to the activity of ghrelin. Also they found that ghrelin regulated metabolic homeostasis through the activation of genes involved in the oxidative phosphorylation pathway.
Leptin, the satiety hormone and insulin signalling in neurons were critical for regulating blood glucose levels and body weight. Simultaneous blocking of these two parameters was proposed as a potential strategy for altering blood glucose levels.
Team members studied obese families and discovered gene variants associated with appetitive behaviour. Four new obesity susceptibility loci were identified while the majority of mutations were associated with loss of function of nerve growth factor-mediated signalling.
Project outcomes have revealed critical factors affecting food intake and body weight control. These could be used to develop novel obesity interventions to treat even childhood obesity.
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