Cargando…

Postnatal Protein Intake as a Determinant of Skeletal Muscle Structure and Function in Mice—A Pilot Study

Sarcopenia is characterised by an age-related decrease in the number of muscle fibres and additional weakening of the remaining fibres, resulting in a reduction in muscle mass and function. Many studies associate poor maternal nutrition during gestation and/or lactation with altered skeletal muscle...

Descripción completa

Detalles Bibliográficos
Autores principales: Giakoumaki, Ifigeneia, Pollock, Natalie, Aljuaid, Turki, Sannicandro, Anthony J., Alameddine, Moussira, Owen, Euan, Myrtziou, Ioanna, Ozanne, Susan E., Kanakis, Ioannis, Goljanek-Whysall, Katarzyna, Vasilaki, Aphrodite
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9369224/
https://www.ncbi.nlm.nih.gov/pubmed/35955948
http://dx.doi.org/10.3390/ijms23158815
_version_ 1784766390469656576
author Giakoumaki, Ifigeneia
Pollock, Natalie
Aljuaid, Turki
Sannicandro, Anthony J.
Alameddine, Moussira
Owen, Euan
Myrtziou, Ioanna
Ozanne, Susan E.
Kanakis, Ioannis
Goljanek-Whysall, Katarzyna
Vasilaki, Aphrodite
author_facet Giakoumaki, Ifigeneia
Pollock, Natalie
Aljuaid, Turki
Sannicandro, Anthony J.
Alameddine, Moussira
Owen, Euan
Myrtziou, Ioanna
Ozanne, Susan E.
Kanakis, Ioannis
Goljanek-Whysall, Katarzyna
Vasilaki, Aphrodite
author_sort Giakoumaki, Ifigeneia
collection PubMed
description Sarcopenia is characterised by an age-related decrease in the number of muscle fibres and additional weakening of the remaining fibres, resulting in a reduction in muscle mass and function. Many studies associate poor maternal nutrition during gestation and/or lactation with altered skeletal muscle homeostasis in the offspring and the development of sarcopenia. The aim of this study was to determine whether the musculoskeletal physiology in offspring born to mouse dams fed a low-protein diet during pregnancy was altered and whether any physiological changes could be modulated by the nutritional protein content in early postnatal stages. Thy1-YFP female mice were fed ad libitum on either a normal (20%) or a low-protein (5%) diet. Newborn pups were cross-fostered to different lactating dams (maintained on a 20% or 5% diet) to generate three groups analysed at weaning (21 days): Normal-to-Normal (NN), Normal-to-Low (NL) and Low-to-Normal (LN). Further offspring were maintained ad libitum on the same diet as during lactation until 12 weeks of age, creating another three groups (NNN, NLL, LNN). Mice on a low protein diet postnatally (NL, NLL) exhibited a significant reduction in body and muscle weight persisting up to 12 weeks, unlike mice on a low protein diet only prenatally (LN, LNN). Muscle fibre size was reduced in mice from the NL but not LN group, showing recovery at 12 weeks of age. Muscle force was reduced in NLL mice, concomitant with changes in the NMJ site and changes in atrophy-related and myosin genes. In addition, μCT scans of mouse tibiae at 12 weeks of age revealed changes in bone mass and morphology, resulting in a higher bone mass in the NLL group than the control NNN group. Finally, changes in the expression of miR-133 in the muscle of NLL mice suggest a regulatory role for this microRNA in muscle development in response to postnatal diet changes. Overall, this data shows that a low maternal protein diet and early postnatal life low-protein intake in mice can impact skeletal muscle physiology and function in early life while postnatal low protein diet favours bone integrity in adulthood.
format Online
Article
Text
id pubmed-9369224
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-93692242022-08-12 Postnatal Protein Intake as a Determinant of Skeletal Muscle Structure and Function in Mice—A Pilot Study Giakoumaki, Ifigeneia Pollock, Natalie Aljuaid, Turki Sannicandro, Anthony J. Alameddine, Moussira Owen, Euan Myrtziou, Ioanna Ozanne, Susan E. Kanakis, Ioannis Goljanek-Whysall, Katarzyna Vasilaki, Aphrodite Int J Mol Sci Article Sarcopenia is characterised by an age-related decrease in the number of muscle fibres and additional weakening of the remaining fibres, resulting in a reduction in muscle mass and function. Many studies associate poor maternal nutrition during gestation and/or lactation with altered skeletal muscle homeostasis in the offspring and the development of sarcopenia. The aim of this study was to determine whether the musculoskeletal physiology in offspring born to mouse dams fed a low-protein diet during pregnancy was altered and whether any physiological changes could be modulated by the nutritional protein content in early postnatal stages. Thy1-YFP female mice were fed ad libitum on either a normal (20%) or a low-protein (5%) diet. Newborn pups were cross-fostered to different lactating dams (maintained on a 20% or 5% diet) to generate three groups analysed at weaning (21 days): Normal-to-Normal (NN), Normal-to-Low (NL) and Low-to-Normal (LN). Further offspring were maintained ad libitum on the same diet as during lactation until 12 weeks of age, creating another three groups (NNN, NLL, LNN). Mice on a low protein diet postnatally (NL, NLL) exhibited a significant reduction in body and muscle weight persisting up to 12 weeks, unlike mice on a low protein diet only prenatally (LN, LNN). Muscle fibre size was reduced in mice from the NL but not LN group, showing recovery at 12 weeks of age. Muscle force was reduced in NLL mice, concomitant with changes in the NMJ site and changes in atrophy-related and myosin genes. In addition, μCT scans of mouse tibiae at 12 weeks of age revealed changes in bone mass and morphology, resulting in a higher bone mass in the NLL group than the control NNN group. Finally, changes in the expression of miR-133 in the muscle of NLL mice suggest a regulatory role for this microRNA in muscle development in response to postnatal diet changes. Overall, this data shows that a low maternal protein diet and early postnatal life low-protein intake in mice can impact skeletal muscle physiology and function in early life while postnatal low protein diet favours bone integrity in adulthood. MDPI 2022-08-08 /pmc/articles/PMC9369224/ /pubmed/35955948 http://dx.doi.org/10.3390/ijms23158815 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Giakoumaki, Ifigeneia
Pollock, Natalie
Aljuaid, Turki
Sannicandro, Anthony J.
Alameddine, Moussira
Owen, Euan
Myrtziou, Ioanna
Ozanne, Susan E.
Kanakis, Ioannis
Goljanek-Whysall, Katarzyna
Vasilaki, Aphrodite
Postnatal Protein Intake as a Determinant of Skeletal Muscle Structure and Function in Mice—A Pilot Study
title Postnatal Protein Intake as a Determinant of Skeletal Muscle Structure and Function in Mice—A Pilot Study
title_full Postnatal Protein Intake as a Determinant of Skeletal Muscle Structure and Function in Mice—A Pilot Study
title_fullStr Postnatal Protein Intake as a Determinant of Skeletal Muscle Structure and Function in Mice—A Pilot Study
title_full_unstemmed Postnatal Protein Intake as a Determinant of Skeletal Muscle Structure and Function in Mice—A Pilot Study
title_short Postnatal Protein Intake as a Determinant of Skeletal Muscle Structure and Function in Mice—A Pilot Study
title_sort postnatal protein intake as a determinant of skeletal muscle structure and function in mice—a pilot study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9369224/
https://www.ncbi.nlm.nih.gov/pubmed/35955948
http://dx.doi.org/10.3390/ijms23158815
work_keys_str_mv AT giakoumakiifigeneia postnatalproteinintakeasadeterminantofskeletalmusclestructureandfunctioninmiceapilotstudy
AT pollocknatalie postnatalproteinintakeasadeterminantofskeletalmusclestructureandfunctioninmiceapilotstudy
AT aljuaidturki postnatalproteinintakeasadeterminantofskeletalmusclestructureandfunctioninmiceapilotstudy
AT sannicandroanthonyj postnatalproteinintakeasadeterminantofskeletalmusclestructureandfunctioninmiceapilotstudy
AT alameddinemoussira postnatalproteinintakeasadeterminantofskeletalmusclestructureandfunctioninmiceapilotstudy
AT oweneuan postnatalproteinintakeasadeterminantofskeletalmusclestructureandfunctioninmiceapilotstudy
AT myrtziouioanna postnatalproteinintakeasadeterminantofskeletalmusclestructureandfunctioninmiceapilotstudy
AT ozannesusane postnatalproteinintakeasadeterminantofskeletalmusclestructureandfunctioninmiceapilotstudy
AT kanakisioannis postnatalproteinintakeasadeterminantofskeletalmusclestructureandfunctioninmiceapilotstudy
AT goljanekwhysallkatarzyna postnatalproteinintakeasadeterminantofskeletalmusclestructureandfunctioninmiceapilotstudy
AT vasilakiaphrodite postnatalproteinintakeasadeterminantofskeletalmusclestructureandfunctioninmiceapilotstudy