GPR43 AND OBESITY

Short chain fatty acids and GPR43 in human health and disease

 Coordinatore IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE 

 Organization address address: SOUTH KENSINGTON CAMPUS EXHIBITION ROAD
city: LONDON
postcode: SW7 2AZ

contact info
Titolo: Ms.
Nome: Tatjana
Cognome: Palalic
Email: send email
Telefono: 442076000000
Fax: 442076000000

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 75˙000 €
 EC contributo 75˙000 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2009-RG
 Funding Scheme MC-IRG
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-04-01   -   2013-03-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE

 Organization address address: SOUTH KENSINGTON CAMPUS EXHIBITION ROAD
city: LONDON
postcode: SW7 2AZ

contact info
Titolo: Ms.
Nome: Tatjana
Cognome: Palalic
Email: send email
Telefono: 442076000000
Fax: 442076000000

UK (LONDON) coordinator 75˙000.00

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

scfa    reduces    carbohydrates    release    receptor    gpr    fermentation    immune    diabetes    peptide    cells    obesity    appetite   

 Obiettivo del progetto (Objective)

'These studies will determine the physiological impact of short chain fatty acids (SCFA) which activate the G-coupled protein receptor 43 (GPR43) as dietary supplementation in treating obesity and type 2 diabetes. Non-digestible carbohydrates (NDC) are carbohydrates which are indigestible in the small intestine, but are broken down in the colon by the fermentation process of bacteria. SCFA are the major products of carbohydrate fermentation and bind to a receptor called GPR43 which is expressed on adipocytes, immune cells, pancreatic beta-cells and enteroendocrine cells that release appetite-suppressing hormones glucagon like peptide-1 (GLP-1) and peptide YY (PYY). Therefore, it is suggestive that this receptor provides a cross-talk between different organs and tissues, linking metabolism with the innate immune system. These studies aim to test the hypothesis that administration of the SCFA propionate reduces appetite by inducing anorectic gut hormone release, improves glucose stimulated insulin secretion, reduces body weight, induces adipocyte proliferation and differentiation, and regulates activation of the immune system and systemic inflammation. Should these studies prove positive then this work will propose a novel treatment option for obesity and type 2 diabetes.'

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