Cargando…

Postnatal growth retardation is associated with intestinal mucosa mitochondrial dysfunction and aberrant energy status in piglets

Individuals with postnatal growth retardation (PGR) are prone to developing chronic disease. Abnormal development in small intestine is casually implicated in impaired growth performance. However, the exact mechanism is still unknown. In this present study, PGR piglets (aged 42 days) were employed a...

Descripción completa

Detalles Bibliográficos
Autores principales: Qi, Ming, Wang, Jing, Tan, Bie, Liao, Simeng, Long, Cimin, Yin, Yulong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520312/
https://www.ncbi.nlm.nih.gov/pubmed/32667125
http://dx.doi.org/10.1111/jcmm.15621
_version_ 1783587760072818688
author Qi, Ming
Wang, Jing
Tan, Bie
Liao, Simeng
Long, Cimin
Yin, Yulong
author_facet Qi, Ming
Wang, Jing
Tan, Bie
Liao, Simeng
Long, Cimin
Yin, Yulong
author_sort Qi, Ming
collection PubMed
description Individuals with postnatal growth retardation (PGR) are prone to developing chronic disease. Abnormal development in small intestine is casually implicated in impaired growth performance. However, the exact mechanism is still unknown. In this present study, PGR piglets (aged 42 days) were employed as a good model to analyse changes in nutrient absorption and energy metabolism in the intestinal mucosa. The results showed lower serum concentrations of free amino acids, and lipid metabolites in PGR piglets, which were in accordance with the down‐regulated mRNA expressions involved in fatty acid and amino acid transporters in the jejunal and ileal mucosa. The decreased activities of digestive enzymes and the marked swelling in mitochondria were also observed in the PGR piglets. In addition, it was found that lower ATP production, higher AMP/ATP ratio, deteriorated mitochondrial complex III and ATP synthase, and decreased manganese superoxide dismutase activity in the intestinal mucosa of PGR piglets. Furthermore, altered gene expression involved in energy metabolism, accompanied by decreases in the protein abundance of SIRT1, PGC‐1α and PPARγ, as well as phosphorylations of AMPKα, mTOR, P70S6K and 4E‐BP1 were observed in intestinal mucosa of PGR piglets. In conclusion, decreased capability of nutrient absorption, mitochondrial dysfunction, and aberrant energy status in the jejunal and ileal mucosa may contribute to PGR piglets.
format Online
Article
Text
id pubmed-7520312
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-75203122020-09-30 Postnatal growth retardation is associated with intestinal mucosa mitochondrial dysfunction and aberrant energy status in piglets Qi, Ming Wang, Jing Tan, Bie Liao, Simeng Long, Cimin Yin, Yulong J Cell Mol Med Original Articles Individuals with postnatal growth retardation (PGR) are prone to developing chronic disease. Abnormal development in small intestine is casually implicated in impaired growth performance. However, the exact mechanism is still unknown. In this present study, PGR piglets (aged 42 days) were employed as a good model to analyse changes in nutrient absorption and energy metabolism in the intestinal mucosa. The results showed lower serum concentrations of free amino acids, and lipid metabolites in PGR piglets, which were in accordance with the down‐regulated mRNA expressions involved in fatty acid and amino acid transporters in the jejunal and ileal mucosa. The decreased activities of digestive enzymes and the marked swelling in mitochondria were also observed in the PGR piglets. In addition, it was found that lower ATP production, higher AMP/ATP ratio, deteriorated mitochondrial complex III and ATP synthase, and decreased manganese superoxide dismutase activity in the intestinal mucosa of PGR piglets. Furthermore, altered gene expression involved in energy metabolism, accompanied by decreases in the protein abundance of SIRT1, PGC‐1α and PPARγ, as well as phosphorylations of AMPKα, mTOR, P70S6K and 4E‐BP1 were observed in intestinal mucosa of PGR piglets. In conclusion, decreased capability of nutrient absorption, mitochondrial dysfunction, and aberrant energy status in the jejunal and ileal mucosa may contribute to PGR piglets. John Wiley and Sons Inc. 2020-07-15 2020-09 /pmc/articles/PMC7520312/ /pubmed/32667125 http://dx.doi.org/10.1111/jcmm.15621 Text en © 2020 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Qi, Ming
Wang, Jing
Tan, Bie
Liao, Simeng
Long, Cimin
Yin, Yulong
Postnatal growth retardation is associated with intestinal mucosa mitochondrial dysfunction and aberrant energy status in piglets
title Postnatal growth retardation is associated with intestinal mucosa mitochondrial dysfunction and aberrant energy status in piglets
title_full Postnatal growth retardation is associated with intestinal mucosa mitochondrial dysfunction and aberrant energy status in piglets
title_fullStr Postnatal growth retardation is associated with intestinal mucosa mitochondrial dysfunction and aberrant energy status in piglets
title_full_unstemmed Postnatal growth retardation is associated with intestinal mucosa mitochondrial dysfunction and aberrant energy status in piglets
title_short Postnatal growth retardation is associated with intestinal mucosa mitochondrial dysfunction and aberrant energy status in piglets
title_sort postnatal growth retardation is associated with intestinal mucosa mitochondrial dysfunction and aberrant energy status in piglets
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520312/
https://www.ncbi.nlm.nih.gov/pubmed/32667125
http://dx.doi.org/10.1111/jcmm.15621
work_keys_str_mv AT qiming postnatalgrowthretardationisassociatedwithintestinalmucosamitochondrialdysfunctionandaberrantenergystatusinpiglets
AT wangjing postnatalgrowthretardationisassociatedwithintestinalmucosamitochondrialdysfunctionandaberrantenergystatusinpiglets
AT tanbie postnatalgrowthretardationisassociatedwithintestinalmucosamitochondrialdysfunctionandaberrantenergystatusinpiglets
AT liaosimeng postnatalgrowthretardationisassociatedwithintestinalmucosamitochondrialdysfunctionandaberrantenergystatusinpiglets
AT longcimin postnatalgrowthretardationisassociatedwithintestinalmucosamitochondrialdysfunctionandaberrantenergystatusinpiglets
AT yinyulong postnatalgrowthretardationisassociatedwithintestinalmucosamitochondrialdysfunctionandaberrantenergystatusinpiglets