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Immunization Against Active Ghrelin Using Virus-Like Particles for Obesity Treatment

Ghrelin is a gut hormone that stimulates food intake. In physiological conditions, ghrelin plasma levels rise with fasting and decrease after meals. Obese individuals have low fasting ghrelin levels that rise after food restriction, which is pointed out as a reason for the difficulty in maintaining...

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Autores principales: Andrade, Sara, Pinho, Filipa, Ribeiro, Andreia M, Carreira, Marcos, Casanueva, Felipe F, Roy, Polly, Monteiro, Mariana P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850261/
https://www.ncbi.nlm.nih.gov/pubmed/23859551
http://dx.doi.org/10.2174/13816128113199990506
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author Andrade, Sara
Pinho, Filipa
Ribeiro, Andreia M
Carreira, Marcos
Casanueva, Felipe F
Roy, Polly
Monteiro, Mariana P
author_facet Andrade, Sara
Pinho, Filipa
Ribeiro, Andreia M
Carreira, Marcos
Casanueva, Felipe F
Roy, Polly
Monteiro, Mariana P
author_sort Andrade, Sara
collection PubMed
description Ghrelin is a gut hormone that stimulates food intake. In physiological conditions, ghrelin plasma levels rise with fasting and decrease after meals. Obese individuals have low fasting ghrelin levels that rise after food restriction, which is pointed out as a reason for the difficulty in maintaining weight loss. Some bariatric surgery procedures prevent rise in ghrelin levels with weight loss and this has been hypothesised to contribute to the long-term success of the treatment. The main goal of this study was to develop a safe and effective anti-ghrelin vaccine for obesity, through the chemical conjugation of ghrelin with a virus like particle, namely NS1 protein tubules from the Bluetongue Virus (BTV) using a hetero-bifunctional cross linker. Male adult C57BL/6 mice, with a normal weight and with diet-induced obesity (DIO), were randomized into six weight matched groups (n=6/group) and each group of mice received three intra-peritoneal injections with two weeks intervals, containing either 75 µg of ghrelin-NS1 immunoconjugate, 75 µg of NS1 or PBS. Our data show that immunized animals present increasing titres of anti-ghrelin antibodies, while their cumulative food intake significantly decreased and energy expenditure was significantly enhanced, although there were no significative changes in body weight.Vaccinated DIO mice also displayed significant decrease of NPY gene expression in the basal hypothalamus reflecting a decrease in central orexigenic signals. This study suggests that this anti-ghrelin vaccine has a positive impact on energy homeostasis and may be an additional therapeutical tool to be used with diet and exercise for obesity treatment.
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spelling pubmed-38502612013-12-06 Immunization Against Active Ghrelin Using Virus-Like Particles for Obesity Treatment Andrade, Sara Pinho, Filipa Ribeiro, Andreia M Carreira, Marcos Casanueva, Felipe F Roy, Polly Monteiro, Mariana P Curr Pharm Des Article Ghrelin is a gut hormone that stimulates food intake. In physiological conditions, ghrelin plasma levels rise with fasting and decrease after meals. Obese individuals have low fasting ghrelin levels that rise after food restriction, which is pointed out as a reason for the difficulty in maintaining weight loss. Some bariatric surgery procedures prevent rise in ghrelin levels with weight loss and this has been hypothesised to contribute to the long-term success of the treatment. The main goal of this study was to develop a safe and effective anti-ghrelin vaccine for obesity, through the chemical conjugation of ghrelin with a virus like particle, namely NS1 protein tubules from the Bluetongue Virus (BTV) using a hetero-bifunctional cross linker. Male adult C57BL/6 mice, with a normal weight and with diet-induced obesity (DIO), were randomized into six weight matched groups (n=6/group) and each group of mice received three intra-peritoneal injections with two weeks intervals, containing either 75 µg of ghrelin-NS1 immunoconjugate, 75 µg of NS1 or PBS. Our data show that immunized animals present increasing titres of anti-ghrelin antibodies, while their cumulative food intake significantly decreased and energy expenditure was significantly enhanced, although there were no significative changes in body weight.Vaccinated DIO mice also displayed significant decrease of NPY gene expression in the basal hypothalamus reflecting a decrease in central orexigenic signals. This study suggests that this anti-ghrelin vaccine has a positive impact on energy homeostasis and may be an additional therapeutical tool to be used with diet and exercise for obesity treatment. Bentham Science Publishers 2013-11 2013-11 /pmc/articles/PMC3850261/ /pubmed/23859551 http://dx.doi.org/10.2174/13816128113199990506 Text en © 2013 Bentham Science Publishers http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.5/), which permits unrestrictive use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Andrade, Sara
Pinho, Filipa
Ribeiro, Andreia M
Carreira, Marcos
Casanueva, Felipe F
Roy, Polly
Monteiro, Mariana P
Immunization Against Active Ghrelin Using Virus-Like Particles for Obesity Treatment
title Immunization Against Active Ghrelin Using Virus-Like Particles for Obesity Treatment
title_full Immunization Against Active Ghrelin Using Virus-Like Particles for Obesity Treatment
title_fullStr Immunization Against Active Ghrelin Using Virus-Like Particles for Obesity Treatment
title_full_unstemmed Immunization Against Active Ghrelin Using Virus-Like Particles for Obesity Treatment
title_short Immunization Against Active Ghrelin Using Virus-Like Particles for Obesity Treatment
title_sort immunization against active ghrelin using virus-like particles for obesity treatment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850261/
https://www.ncbi.nlm.nih.gov/pubmed/23859551
http://dx.doi.org/10.2174/13816128113199990506
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