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Enhancement of immune maturation in suckling rats by leptin and adiponectin supplementation
Leptin and adiponectin, adipokines present in breast milk, have shown immunomodulatory properties. The current study aimed to ascertain whether a nutritional supplementation with leptin or adiponectin in neonatal rats was able to influence the maturation of the systemic immune response in early life...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370875/ https://www.ncbi.nlm.nih.gov/pubmed/30742004 http://dx.doi.org/10.1038/s41598-018-38418-1 |
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author | Grases-Pintó, Blanca Abril-Gil, Mar Castell, Margarida Pérez-Cano, Francisco J. Franch, Àngels |
author_facet | Grases-Pintó, Blanca Abril-Gil, Mar Castell, Margarida Pérez-Cano, Francisco J. Franch, Àngels |
author_sort | Grases-Pintó, Blanca |
collection | PubMed |
description | Leptin and adiponectin, adipokines present in breast milk, have shown immunomodulatory properties. The current study aimed to ascertain whether a nutritional supplementation with leptin or adiponectin in neonatal rats was able to influence the maturation of the systemic immune response in early life. To achieve this, suckling Wistar rats were supplemented with either leptin (0.7 μg/kg/day) or adiponectin (35 μg/kg/day) during the whole suckling period. Plasmatic immunoglobulins were quantified, and spleen lymphocyte composition and their ability to proliferate and release cytokines were evaluated during (day 14) and at the end (day 21) of the suckling period. Rats fed with either adipokine showed higher plasma IgM and IgG1 concentrations and adiponectin supplementation also increased IgG2a at both studied days (P < 0.05). With regard to the lymphocyte composition, both adipokine supplementations increased T cell proportion and both CD4(+) and CD8(+) T cell subsets after two weeks of supplementation (P < 0.05). Moreover, only leptin administration increased NK and NKT cell proportions at the end of the suckling period. Finally, both adipokines influenced the cytokine secretion pattern by splenocytes. In conclusion, these results suggest that leptin and adiponectin play a role in the maturation of the systemic immune response during the suckling period. |
format | Online Article Text |
id | pubmed-6370875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63708752019-02-15 Enhancement of immune maturation in suckling rats by leptin and adiponectin supplementation Grases-Pintó, Blanca Abril-Gil, Mar Castell, Margarida Pérez-Cano, Francisco J. Franch, Àngels Sci Rep Article Leptin and adiponectin, adipokines present in breast milk, have shown immunomodulatory properties. The current study aimed to ascertain whether a nutritional supplementation with leptin or adiponectin in neonatal rats was able to influence the maturation of the systemic immune response in early life. To achieve this, suckling Wistar rats were supplemented with either leptin (0.7 μg/kg/day) or adiponectin (35 μg/kg/day) during the whole suckling period. Plasmatic immunoglobulins were quantified, and spleen lymphocyte composition and their ability to proliferate and release cytokines were evaluated during (day 14) and at the end (day 21) of the suckling period. Rats fed with either adipokine showed higher plasma IgM and IgG1 concentrations and adiponectin supplementation also increased IgG2a at both studied days (P < 0.05). With regard to the lymphocyte composition, both adipokine supplementations increased T cell proportion and both CD4(+) and CD8(+) T cell subsets after two weeks of supplementation (P < 0.05). Moreover, only leptin administration increased NK and NKT cell proportions at the end of the suckling period. Finally, both adipokines influenced the cytokine secretion pattern by splenocytes. In conclusion, these results suggest that leptin and adiponectin play a role in the maturation of the systemic immune response during the suckling period. Nature Publishing Group UK 2019-02-11 /pmc/articles/PMC6370875/ /pubmed/30742004 http://dx.doi.org/10.1038/s41598-018-38418-1 Text en © The Author(s) 2019 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 Grases-Pintó, Blanca Abril-Gil, Mar Castell, Margarida Pérez-Cano, Francisco J. Franch, Àngels Enhancement of immune maturation in suckling rats by leptin and adiponectin supplementation |
title | Enhancement of immune maturation in suckling rats by leptin and adiponectin supplementation |
title_full | Enhancement of immune maturation in suckling rats by leptin and adiponectin supplementation |
title_fullStr | Enhancement of immune maturation in suckling rats by leptin and adiponectin supplementation |
title_full_unstemmed | Enhancement of immune maturation in suckling rats by leptin and adiponectin supplementation |
title_short | Enhancement of immune maturation in suckling rats by leptin and adiponectin supplementation |
title_sort | enhancement of immune maturation in suckling rats by leptin and adiponectin supplementation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370875/ https://www.ncbi.nlm.nih.gov/pubmed/30742004 http://dx.doi.org/10.1038/s41598-018-38418-1 |
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