Cargando…

Preclinical Evaluation of a Food-Derived Functional Ingredient to Address Skeletal Muscle Atrophy

Skeletal muscle is the metabolic powerhouse of the body, however, dysregulation of the mechanisms involved in skeletal muscle mass maintenance can have devastating effects leading to many metabolic and physiological diseases. The lack of effective solutions makes finding a validated nutritional inte...

Descripción completa

Detalles Bibliográficos
Autores principales: Cal, Roi, Davis, Heidi, Kerr, Alish, Wall, Audrey, Molloy, Brendan, Chauhan, Sweeny, Trajkovic, Sanja, Holyer, Ian, Adelfio, Alessandro, Khaldi, Nora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469066/
https://www.ncbi.nlm.nih.gov/pubmed/32751276
http://dx.doi.org/10.3390/nu12082274
_version_ 1783578352156672000
author Cal, Roi
Davis, Heidi
Kerr, Alish
Wall, Audrey
Molloy, Brendan
Chauhan, Sweeny
Trajkovic, Sanja
Holyer, Ian
Adelfio, Alessandro
Khaldi, Nora
author_facet Cal, Roi
Davis, Heidi
Kerr, Alish
Wall, Audrey
Molloy, Brendan
Chauhan, Sweeny
Trajkovic, Sanja
Holyer, Ian
Adelfio, Alessandro
Khaldi, Nora
author_sort Cal, Roi
collection PubMed
description Skeletal muscle is the metabolic powerhouse of the body, however, dysregulation of the mechanisms involved in skeletal muscle mass maintenance can have devastating effects leading to many metabolic and physiological diseases. The lack of effective solutions makes finding a validated nutritional intervention an urgent unmet medical need. In vitro testing in murine skeletal muscle cells and human macrophages was carried out to determine the effect of a hydrolysate derived from vicia faba (PeptiStrong: NPN_1) against phosphorylated S6, atrophy gene expression, and tumour necrosis factor alpha (TNF-α) secretion, respectively. Finally, the efficacy of NPN_1 on attenuating muscle waste in vivo was assessed in an atrophy murine model. Treatment of NPN_1 significantly increased the phosphorylation of S6, downregulated muscle atrophy related genes, and reduced lipopolysaccharide-induced TNF-α release in vitro. In a disuse atrophy murine model, following 18 days of NPN_1 treatment, mice exhibited a significant attenuation of muscle loss in the soleus muscle and increased the integrated expression of Type I and Type IIa fibres. At the RNA level, a significant upregulation of protein synthesis-related genes was observed in the soleus muscle following NPN_1 treatment. In vitro and preclinical results suggest that NPN_1 is an effective bioactive ingredient with great potential to prolong muscle health.
format Online
Article
Text
id pubmed-7469066
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-74690662020-09-04 Preclinical Evaluation of a Food-Derived Functional Ingredient to Address Skeletal Muscle Atrophy Cal, Roi Davis, Heidi Kerr, Alish Wall, Audrey Molloy, Brendan Chauhan, Sweeny Trajkovic, Sanja Holyer, Ian Adelfio, Alessandro Khaldi, Nora Nutrients Article Skeletal muscle is the metabolic powerhouse of the body, however, dysregulation of the mechanisms involved in skeletal muscle mass maintenance can have devastating effects leading to many metabolic and physiological diseases. The lack of effective solutions makes finding a validated nutritional intervention an urgent unmet medical need. In vitro testing in murine skeletal muscle cells and human macrophages was carried out to determine the effect of a hydrolysate derived from vicia faba (PeptiStrong: NPN_1) against phosphorylated S6, atrophy gene expression, and tumour necrosis factor alpha (TNF-α) secretion, respectively. Finally, the efficacy of NPN_1 on attenuating muscle waste in vivo was assessed in an atrophy murine model. Treatment of NPN_1 significantly increased the phosphorylation of S6, downregulated muscle atrophy related genes, and reduced lipopolysaccharide-induced TNF-α release in vitro. In a disuse atrophy murine model, following 18 days of NPN_1 treatment, mice exhibited a significant attenuation of muscle loss in the soleus muscle and increased the integrated expression of Type I and Type IIa fibres. At the RNA level, a significant upregulation of protein synthesis-related genes was observed in the soleus muscle following NPN_1 treatment. In vitro and preclinical results suggest that NPN_1 is an effective bioactive ingredient with great potential to prolong muscle health. MDPI 2020-07-29 /pmc/articles/PMC7469066/ /pubmed/32751276 http://dx.doi.org/10.3390/nu12082274 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cal, Roi
Davis, Heidi
Kerr, Alish
Wall, Audrey
Molloy, Brendan
Chauhan, Sweeny
Trajkovic, Sanja
Holyer, Ian
Adelfio, Alessandro
Khaldi, Nora
Preclinical Evaluation of a Food-Derived Functional Ingredient to Address Skeletal Muscle Atrophy
title Preclinical Evaluation of a Food-Derived Functional Ingredient to Address Skeletal Muscle Atrophy
title_full Preclinical Evaluation of a Food-Derived Functional Ingredient to Address Skeletal Muscle Atrophy
title_fullStr Preclinical Evaluation of a Food-Derived Functional Ingredient to Address Skeletal Muscle Atrophy
title_full_unstemmed Preclinical Evaluation of a Food-Derived Functional Ingredient to Address Skeletal Muscle Atrophy
title_short Preclinical Evaluation of a Food-Derived Functional Ingredient to Address Skeletal Muscle Atrophy
title_sort preclinical evaluation of a food-derived functional ingredient to address skeletal muscle atrophy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469066/
https://www.ncbi.nlm.nih.gov/pubmed/32751276
http://dx.doi.org/10.3390/nu12082274
work_keys_str_mv AT calroi preclinicalevaluationofafoodderivedfunctionalingredienttoaddressskeletalmuscleatrophy
AT davisheidi preclinicalevaluationofafoodderivedfunctionalingredienttoaddressskeletalmuscleatrophy
AT kerralish preclinicalevaluationofafoodderivedfunctionalingredienttoaddressskeletalmuscleatrophy
AT wallaudrey preclinicalevaluationofafoodderivedfunctionalingredienttoaddressskeletalmuscleatrophy
AT molloybrendan preclinicalevaluationofafoodderivedfunctionalingredienttoaddressskeletalmuscleatrophy
AT chauhansweeny preclinicalevaluationofafoodderivedfunctionalingredienttoaddressskeletalmuscleatrophy
AT trajkovicsanja preclinicalevaluationofafoodderivedfunctionalingredienttoaddressskeletalmuscleatrophy
AT holyerian preclinicalevaluationofafoodderivedfunctionalingredienttoaddressskeletalmuscleatrophy
AT adelfioalessandro preclinicalevaluationofafoodderivedfunctionalingredienttoaddressskeletalmuscleatrophy
AT khaldinora preclinicalevaluationofafoodderivedfunctionalingredienttoaddressskeletalmuscleatrophy