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Salivary PYY: A Putative Bypass to Satiety
Peptide YY(3-36) is a satiation hormone released postprandially into the bloodstream from L-endocrine cells in the gut epithelia. In the current report, we demonstrate PYY(3-36) is also present in murine as well as in human saliva. In mice, salivary PYY(3-36) derives from plasma and is also synthesi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3189958/ https://www.ncbi.nlm.nih.gov/pubmed/22028819 http://dx.doi.org/10.1371/journal.pone.0026137 |
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author | Acosta, Andres Hurtado, Maria D. Gorbatyuk, Oleg La Sala, Michael Duncan, David Aslanidi, George Campbell-Thompson, Martha Zhang, Lei Herzog, Herbert Voutetakis, Antonis Baum, Bruce J. Zolotukhin, Sergei |
author_facet | Acosta, Andres Hurtado, Maria D. Gorbatyuk, Oleg La Sala, Michael Duncan, David Aslanidi, George Campbell-Thompson, Martha Zhang, Lei Herzog, Herbert Voutetakis, Antonis Baum, Bruce J. Zolotukhin, Sergei |
author_sort | Acosta, Andres |
collection | PubMed |
description | Peptide YY(3-36) is a satiation hormone released postprandially into the bloodstream from L-endocrine cells in the gut epithelia. In the current report, we demonstrate PYY(3-36) is also present in murine as well as in human saliva. In mice, salivary PYY(3-36) derives from plasma and is also synthesized in the taste cells in taste buds of the tongue. Moreover, the cognate receptor Y2R is abundantly expressed in the basal layer of the progenitor cells of the tongue epithelia and von Ebner's gland. The acute augmentation of salivary PYY(3-36) induced stronger satiation as demonstrated in feeding behavioral studies. The effect is mediated through the activation of the specific Y2 receptor expressed in the lingual epithelial cells. In a long-term study involving diet-induced obese (DIO) mice, a sustained increase in PYY(3-36) was achieved using viral vector-mediated gene delivery targeting salivary glands. The chronic increase in salivary PYY(3-36) resulted in a significant long-term reduction in food intake (FI) and body weight (BW). Thus this study provides evidence for new functions of the previously characterized gut peptide PYY(3-36) suggesting a potential simple and efficient alternative therapeutic approach for the treatment of obesity. |
format | Online Article Text |
id | pubmed-3189958 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31899582011-10-25 Salivary PYY: A Putative Bypass to Satiety Acosta, Andres Hurtado, Maria D. Gorbatyuk, Oleg La Sala, Michael Duncan, David Aslanidi, George Campbell-Thompson, Martha Zhang, Lei Herzog, Herbert Voutetakis, Antonis Baum, Bruce J. Zolotukhin, Sergei PLoS One Research Article Peptide YY(3-36) is a satiation hormone released postprandially into the bloodstream from L-endocrine cells in the gut epithelia. In the current report, we demonstrate PYY(3-36) is also present in murine as well as in human saliva. In mice, salivary PYY(3-36) derives from plasma and is also synthesized in the taste cells in taste buds of the tongue. Moreover, the cognate receptor Y2R is abundantly expressed in the basal layer of the progenitor cells of the tongue epithelia and von Ebner's gland. The acute augmentation of salivary PYY(3-36) induced stronger satiation as demonstrated in feeding behavioral studies. The effect is mediated through the activation of the specific Y2 receptor expressed in the lingual epithelial cells. In a long-term study involving diet-induced obese (DIO) mice, a sustained increase in PYY(3-36) was achieved using viral vector-mediated gene delivery targeting salivary glands. The chronic increase in salivary PYY(3-36) resulted in a significant long-term reduction in food intake (FI) and body weight (BW). Thus this study provides evidence for new functions of the previously characterized gut peptide PYY(3-36) suggesting a potential simple and efficient alternative therapeutic approach for the treatment of obesity. Public Library of Science 2011-10-10 /pmc/articles/PMC3189958/ /pubmed/22028819 http://dx.doi.org/10.1371/journal.pone.0026137 Text en This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Acosta, Andres Hurtado, Maria D. Gorbatyuk, Oleg La Sala, Michael Duncan, David Aslanidi, George Campbell-Thompson, Martha Zhang, Lei Herzog, Herbert Voutetakis, Antonis Baum, Bruce J. Zolotukhin, Sergei Salivary PYY: A Putative Bypass to Satiety |
title | Salivary PYY: A Putative Bypass to Satiety |
title_full | Salivary PYY: A Putative Bypass to Satiety |
title_fullStr | Salivary PYY: A Putative Bypass to Satiety |
title_full_unstemmed | Salivary PYY: A Putative Bypass to Satiety |
title_short | Salivary PYY: A Putative Bypass to Satiety |
title_sort | salivary pyy: a putative bypass to satiety |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3189958/ https://www.ncbi.nlm.nih.gov/pubmed/22028819 http://dx.doi.org/10.1371/journal.pone.0026137 |
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