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Modulation of liver glucose output by free or restricted feeding in the adult rat is independent of litter size
BACKGROUND: Caloric restriction since birth changes glucose metabolism by the liver in overnight-fasted rats to a fed-like pattern, in which glucose output is large but gluconeogenesis is negligible. It was investigated whether these changes could be a residual effect of the nutritional condition du...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6909465/ https://www.ncbi.nlm.nih.gov/pubmed/31857820 http://dx.doi.org/10.1186/s12986-019-0413-0 |
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author | Yamada, Laís Akemi Mariano, Isabela Ramos Sabino, Vanessa Lara Rissi Rabassi, Renan Soares Bataglini, Camila Azevedo, Silvia Carla Santana Ferreira Branquinho, Nayra Thais Delatorre Kurauti, Mirian Ayumi Garcia, Rosângela Fernandes Pedrosa, Maria Montserrat Diaz |
author_facet | Yamada, Laís Akemi Mariano, Isabela Ramos Sabino, Vanessa Lara Rissi Rabassi, Renan Soares Bataglini, Camila Azevedo, Silvia Carla Santana Ferreira Branquinho, Nayra Thais Delatorre Kurauti, Mirian Ayumi Garcia, Rosângela Fernandes Pedrosa, Maria Montserrat Diaz |
author_sort | Yamada, Laís Akemi |
collection | PubMed |
description | BACKGROUND: Caloric restriction since birth changes glucose metabolism by the liver in overnight-fasted rats to a fed-like pattern, in which glucose output is large but gluconeogenesis is negligible. It was investigated whether these changes could be a residual effect of the nutritional condition during lactation and what could be the mechanism of such change. METHODS: Newborn Wistar rat pups were arranged in litters of 6 or 12 (G6 and G12). After weaning, the male pups were divided in: G6L and G12 L, fed freely until the age of 90 days (freely-fed groups); G6R and G12R, given 50% of the GL ingestion (food-restricted groups) until 90 days of age; G6RL and G12RL, given 50% of the GL ingestion until 60 days of age and fed freely until 90 days of age (refed groups). The experimental protocols were carried out at the age of 90 days after overnight fasting. Pairs of groups were compared through t test; other statistical comparisons were made with one-way ANOVA with Tukey post hoc text. RESULTS: Caloric restriction was effective in decreasing body and fat weights, total cholesterol and LDL. These effects were totally or partially reversed after 30 days of refeeding (groups GRL). During liver perfusion, the high glucose output of the GRs was further enhanced by adrenaline (1 μM), but not by lactate infusion. In contrast, in groups G6L, G12 L, G6RL and G12RL glycogenolysis (basal and adrenaline-stimulated glucose output) was low and gluconeogenesis from lactate was significant. A twofold increase in liver content of PKA in group G6R suggests that liver sensitivity to glucagon and adrenaline was higher because of caloric restriction, resulting in enhanced glucose output. CONCLUSIONS: As glucose output was not affected by litter size, liver glucose metabolism in the adult rat, in contrast to other metabolic processes, is not a programmed effect of the nutritional condition during lactation. In addition, the increased expression of PKA points to a higher sensitivity of the animals under caloric restriction to glycogenolytic hormones, a relevant condition for glucose homeostasis during fasting. |
format | Online Article Text |
id | pubmed-6909465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69094652019-12-19 Modulation of liver glucose output by free or restricted feeding in the adult rat is independent of litter size Yamada, Laís Akemi Mariano, Isabela Ramos Sabino, Vanessa Lara Rissi Rabassi, Renan Soares Bataglini, Camila Azevedo, Silvia Carla Santana Ferreira Branquinho, Nayra Thais Delatorre Kurauti, Mirian Ayumi Garcia, Rosângela Fernandes Pedrosa, Maria Montserrat Diaz Nutr Metab (Lond) Research BACKGROUND: Caloric restriction since birth changes glucose metabolism by the liver in overnight-fasted rats to a fed-like pattern, in which glucose output is large but gluconeogenesis is negligible. It was investigated whether these changes could be a residual effect of the nutritional condition during lactation and what could be the mechanism of such change. METHODS: Newborn Wistar rat pups were arranged in litters of 6 or 12 (G6 and G12). After weaning, the male pups were divided in: G6L and G12 L, fed freely until the age of 90 days (freely-fed groups); G6R and G12R, given 50% of the GL ingestion (food-restricted groups) until 90 days of age; G6RL and G12RL, given 50% of the GL ingestion until 60 days of age and fed freely until 90 days of age (refed groups). The experimental protocols were carried out at the age of 90 days after overnight fasting. Pairs of groups were compared through t test; other statistical comparisons were made with one-way ANOVA with Tukey post hoc text. RESULTS: Caloric restriction was effective in decreasing body and fat weights, total cholesterol and LDL. These effects were totally or partially reversed after 30 days of refeeding (groups GRL). During liver perfusion, the high glucose output of the GRs was further enhanced by adrenaline (1 μM), but not by lactate infusion. In contrast, in groups G6L, G12 L, G6RL and G12RL glycogenolysis (basal and adrenaline-stimulated glucose output) was low and gluconeogenesis from lactate was significant. A twofold increase in liver content of PKA in group G6R suggests that liver sensitivity to glucagon and adrenaline was higher because of caloric restriction, resulting in enhanced glucose output. CONCLUSIONS: As glucose output was not affected by litter size, liver glucose metabolism in the adult rat, in contrast to other metabolic processes, is not a programmed effect of the nutritional condition during lactation. In addition, the increased expression of PKA points to a higher sensitivity of the animals under caloric restriction to glycogenolytic hormones, a relevant condition for glucose homeostasis during fasting. BioMed Central 2019-12-12 /pmc/articles/PMC6909465/ /pubmed/31857820 http://dx.doi.org/10.1186/s12986-019-0413-0 Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Yamada, Laís Akemi Mariano, Isabela Ramos Sabino, Vanessa Lara Rissi Rabassi, Renan Soares Bataglini, Camila Azevedo, Silvia Carla Santana Ferreira Branquinho, Nayra Thais Delatorre Kurauti, Mirian Ayumi Garcia, Rosângela Fernandes Pedrosa, Maria Montserrat Diaz Modulation of liver glucose output by free or restricted feeding in the adult rat is independent of litter size |
title | Modulation of liver glucose output by free or restricted feeding in the adult rat is independent of litter size |
title_full | Modulation of liver glucose output by free or restricted feeding in the adult rat is independent of litter size |
title_fullStr | Modulation of liver glucose output by free or restricted feeding in the adult rat is independent of litter size |
title_full_unstemmed | Modulation of liver glucose output by free or restricted feeding in the adult rat is independent of litter size |
title_short | Modulation of liver glucose output by free or restricted feeding in the adult rat is independent of litter size |
title_sort | modulation of liver glucose output by free or restricted feeding in the adult rat is independent of litter size |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6909465/ https://www.ncbi.nlm.nih.gov/pubmed/31857820 http://dx.doi.org/10.1186/s12986-019-0413-0 |
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