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Low-quality protein modulates inflammatory markers and the response to lipopolysaccharide insult: the case of lysine

The relationship between non-communicable diseases and eating behaviour has long been attributed to a surplus of food and energy. However, the increase in the prevalence of non-communicable disease and their underlying low-grade inflammatory milieu among people of low socio-economic status has highl...

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Autores principales: El-Mallah, Carla, Ragi, Marie-Elizabeth E., Eid, Assaad, Obeid, Omar A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10442798/
https://www.ncbi.nlm.nih.gov/pubmed/36597807
http://dx.doi.org/10.1017/S0007114522004068
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author El-Mallah, Carla
Ragi, Marie-Elizabeth E.
Eid, Assaad
Obeid, Omar A.
author_facet El-Mallah, Carla
Ragi, Marie-Elizabeth E.
Eid, Assaad
Obeid, Omar A.
author_sort El-Mallah, Carla
collection PubMed
description The relationship between non-communicable diseases and eating behaviour has long been attributed to a surplus of food and energy. However, the increase in the prevalence of non-communicable disease and their underlying low-grade inflammatory milieu among people of low socio-economic status has highlighted the existence of a confounding factor. In this work, we aim to study the effect of lysine deficiency on some inflammatory markers in the absence or presence of an inflammatory insult (lipopolysaccharide (LPS)). For this purpose, thirty-two 5-week-old male Sprague Dawley rats were randomly distributed into four groups: (1) control diet, (2) control diet+LPS, (3) lysine-deficient diet and (4) lysine-deficient diet + LPS. Groups were only allowed their experimental diets for 4 weeks, during which LPS (50 µg/kg) or saline injections were administered intraperitoneally three times per week. The study showed that lysine deficiency blunted growth and body compartments development, decreased albumin production and elevated liver C-reactive protein (CRP) expression, independently of IL-6 and IL-1β, the main precursors of CRP. Also, the insufficient levels of lysine in the diet increased hyperactivity and triggered an anxiety-like behaviour, exacerbated with LPS. This work presents evidence that various physiological changes are associated with the absence of a sufficient amount of lysine in the diet and can potentially increase the risk factor for diseases. Thus, the increment in non-communicable disease among the low socio-economic status populations, who heavily rely on cereals as a main source of protein, can be, at least partially, blamed on low lysine availability in diets.
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spelling pubmed-104427982023-08-23 Low-quality protein modulates inflammatory markers and the response to lipopolysaccharide insult: the case of lysine El-Mallah, Carla Ragi, Marie-Elizabeth E. Eid, Assaad Obeid, Omar A. Br J Nutr Research Article The relationship between non-communicable diseases and eating behaviour has long been attributed to a surplus of food and energy. However, the increase in the prevalence of non-communicable disease and their underlying low-grade inflammatory milieu among people of low socio-economic status has highlighted the existence of a confounding factor. In this work, we aim to study the effect of lysine deficiency on some inflammatory markers in the absence or presence of an inflammatory insult (lipopolysaccharide (LPS)). For this purpose, thirty-two 5-week-old male Sprague Dawley rats were randomly distributed into four groups: (1) control diet, (2) control diet+LPS, (3) lysine-deficient diet and (4) lysine-deficient diet + LPS. Groups were only allowed their experimental diets for 4 weeks, during which LPS (50 µg/kg) or saline injections were administered intraperitoneally three times per week. The study showed that lysine deficiency blunted growth and body compartments development, decreased albumin production and elevated liver C-reactive protein (CRP) expression, independently of IL-6 and IL-1β, the main precursors of CRP. Also, the insufficient levels of lysine in the diet increased hyperactivity and triggered an anxiety-like behaviour, exacerbated with LPS. This work presents evidence that various physiological changes are associated with the absence of a sufficient amount of lysine in the diet and can potentially increase the risk factor for diseases. Thus, the increment in non-communicable disease among the low socio-economic status populations, who heavily rely on cereals as a main source of protein, can be, at least partially, blamed on low lysine availability in diets. Cambridge University Press 2023-09-28 2023-01-04 /pmc/articles/PMC10442798/ /pubmed/36597807 http://dx.doi.org/10.1017/S0007114522004068 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
spellingShingle Research Article
El-Mallah, Carla
Ragi, Marie-Elizabeth E.
Eid, Assaad
Obeid, Omar A.
Low-quality protein modulates inflammatory markers and the response to lipopolysaccharide insult: the case of lysine
title Low-quality protein modulates inflammatory markers and the response to lipopolysaccharide insult: the case of lysine
title_full Low-quality protein modulates inflammatory markers and the response to lipopolysaccharide insult: the case of lysine
title_fullStr Low-quality protein modulates inflammatory markers and the response to lipopolysaccharide insult: the case of lysine
title_full_unstemmed Low-quality protein modulates inflammatory markers and the response to lipopolysaccharide insult: the case of lysine
title_short Low-quality protein modulates inflammatory markers and the response to lipopolysaccharide insult: the case of lysine
title_sort low-quality protein modulates inflammatory markers and the response to lipopolysaccharide insult: the case of lysine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10442798/
https://www.ncbi.nlm.nih.gov/pubmed/36597807
http://dx.doi.org/10.1017/S0007114522004068
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