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Feeding and food availability modulate brain-derived neurotrophic factor, an orexigen with metabolic roles in zebrafish
Emerging findings point to a role for brain-derived neurotrophic factor (BDNF) on feeding in mammals. However, its role on energy balance is unclear. Moreover, whether BDNF regulates energy homeostasis in non-mammals remain unknown. This research aimed to determine whether BDNF is a metabolic peptid...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329848/ https://www.ncbi.nlm.nih.gov/pubmed/32612127 http://dx.doi.org/10.1038/s41598-020-67535-z |
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author | Blanco, Ayelén Melisa Bertucci, Juan Ignacio Hatef, Azadeh Unniappan, Suraj |
author_facet | Blanco, Ayelén Melisa Bertucci, Juan Ignacio Hatef, Azadeh Unniappan, Suraj |
author_sort | Blanco, Ayelén Melisa |
collection | PubMed |
description | Emerging findings point to a role for brain-derived neurotrophic factor (BDNF) on feeding in mammals. However, its role on energy balance is unclear. Moreover, whether BDNF regulates energy homeostasis in non-mammals remain unknown. This research aimed to determine whether BDNF is a metabolic peptide in zebrafish. Our results demonstrate that BDNF mRNAs and protein, as well as mRNAs encoding its receptors trkb2, p75ntra and p75ntrb, are detectable in the zebrafish brain, foregut and liver. Intraperitoneal injection of BDNF increased food intake at 1, 2 and 6 h post-administration, and caused an upregulation of brain npy, agrp and orexin, foregut ghrelin, and hepatic leptin mRNAs, and a reduction in brain nucb2. Fasting for 7 days increased bdnf and p75ntrb mRNAs in the foregut, while decreased bdnf, trkb2, p75ntra and p75ntrb mRNAs in the brain and liver. Additionally, the expression of bdnf and its receptors increased preprandially, and decreased after a meal in the foregut and liver. Finally, we observed BDNF-induced changes in the expression and/or activity of enzymes involved in glucose and lipid metabolism in the liver. Overall, present results indicate that BDNF is a novel regulator of appetite and metabolism in fish, which is modulated by energy intake and food availability. |
format | Online Article Text |
id | pubmed-7329848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73298482020-07-06 Feeding and food availability modulate brain-derived neurotrophic factor, an orexigen with metabolic roles in zebrafish Blanco, Ayelén Melisa Bertucci, Juan Ignacio Hatef, Azadeh Unniappan, Suraj Sci Rep Article Emerging findings point to a role for brain-derived neurotrophic factor (BDNF) on feeding in mammals. However, its role on energy balance is unclear. Moreover, whether BDNF regulates energy homeostasis in non-mammals remain unknown. This research aimed to determine whether BDNF is a metabolic peptide in zebrafish. Our results demonstrate that BDNF mRNAs and protein, as well as mRNAs encoding its receptors trkb2, p75ntra and p75ntrb, are detectable in the zebrafish brain, foregut and liver. Intraperitoneal injection of BDNF increased food intake at 1, 2 and 6 h post-administration, and caused an upregulation of brain npy, agrp and orexin, foregut ghrelin, and hepatic leptin mRNAs, and a reduction in brain nucb2. Fasting for 7 days increased bdnf and p75ntrb mRNAs in the foregut, while decreased bdnf, trkb2, p75ntra and p75ntrb mRNAs in the brain and liver. Additionally, the expression of bdnf and its receptors increased preprandially, and decreased after a meal in the foregut and liver. Finally, we observed BDNF-induced changes in the expression and/or activity of enzymes involved in glucose and lipid metabolism in the liver. Overall, present results indicate that BDNF is a novel regulator of appetite and metabolism in fish, which is modulated by energy intake and food availability. Nature Publishing Group UK 2020-07-01 /pmc/articles/PMC7329848/ /pubmed/32612127 http://dx.doi.org/10.1038/s41598-020-67535-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Blanco, Ayelén Melisa Bertucci, Juan Ignacio Hatef, Azadeh Unniappan, Suraj Feeding and food availability modulate brain-derived neurotrophic factor, an orexigen with metabolic roles in zebrafish |
title | Feeding and food availability modulate brain-derived neurotrophic factor, an orexigen with metabolic roles in zebrafish |
title_full | Feeding and food availability modulate brain-derived neurotrophic factor, an orexigen with metabolic roles in zebrafish |
title_fullStr | Feeding and food availability modulate brain-derived neurotrophic factor, an orexigen with metabolic roles in zebrafish |
title_full_unstemmed | Feeding and food availability modulate brain-derived neurotrophic factor, an orexigen with metabolic roles in zebrafish |
title_short | Feeding and food availability modulate brain-derived neurotrophic factor, an orexigen with metabolic roles in zebrafish |
title_sort | feeding and food availability modulate brain-derived neurotrophic factor, an orexigen with metabolic roles in zebrafish |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329848/ https://www.ncbi.nlm.nih.gov/pubmed/32612127 http://dx.doi.org/10.1038/s41598-020-67535-z |
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