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Potential Defence Mechanisms Triggered by Monosodium Glutamate Sub-Chronic Consumption in Two-Year-Old Wistar Rats

Monosodium glutamate (MSG) is the sodium salt of glutamic acid (GLA), used as a flavour enhancer. MSG is considered a controversial substance. It is incriminated in disturbing the antioxidant system, but also has beneficial effects, as GLA metabolism plays a crucial role in homeostasis. This study h...

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Autores principales: Moldovan, Octavia-Laura, Vari, Camil-Eugen, Tero-Vescan, Amelia, Cotoi, Ovidiu Simion, Cocuz, Iuliu Gabriel, Tabaran, Flaviu Alexandru, Pop, Romelia, Fülöp, Ibolya, Chis, Rafael Florin, Lungu, Ioana-Andreea, Rusu, Aura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10610236/
https://www.ncbi.nlm.nih.gov/pubmed/37892513
http://dx.doi.org/10.3390/nu15204436
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author Moldovan, Octavia-Laura
Vari, Camil-Eugen
Tero-Vescan, Amelia
Cotoi, Ovidiu Simion
Cocuz, Iuliu Gabriel
Tabaran, Flaviu Alexandru
Pop, Romelia
Fülöp, Ibolya
Chis, Rafael Florin
Lungu, Ioana-Andreea
Rusu, Aura
author_facet Moldovan, Octavia-Laura
Vari, Camil-Eugen
Tero-Vescan, Amelia
Cotoi, Ovidiu Simion
Cocuz, Iuliu Gabriel
Tabaran, Flaviu Alexandru
Pop, Romelia
Fülöp, Ibolya
Chis, Rafael Florin
Lungu, Ioana-Andreea
Rusu, Aura
author_sort Moldovan, Octavia-Laura
collection PubMed
description Monosodium glutamate (MSG) is the sodium salt of glutamic acid (GLA), used as a flavour enhancer. MSG is considered a controversial substance. It is incriminated in disturbing the antioxidant system, but also has beneficial effects, as GLA metabolism plays a crucial role in homeostasis. This study highlights which positive or negative aspects of MSG sub-chronic consumption are better reflected in subjects potentially affected by advanced age. Daily doses of MSG were administered to four groups of two-year-old Wistar rats for 90 days: (I) 185 mg/kg bw, (II) 1500 mg/kg bw, (III) 3000 mg/kg bw and (IV) 6000 mg/kg bw, compared to a MSG non-consumer group. Aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase, direct and total bilirubin, total cholesterol, triglycerides, creatinine and urea levels were analysed; stomach, liver and kidney samples were subjected to histopathological analysis. Although, in most cases, there were no statistical differences, interesting aspects of the dose–effect relationship were observed. After MSG sub-chronic consumption, the positive aspects of GLA seem to be reflected better than the negative ones. The hormesis effect, with low-level reactive oxygen species’ protective effects and GLA metabolism, may represent the hypothesis of a potential defence mechanism triggered by MSG sub-chronic consumption in ageing rats.
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spelling pubmed-106102362023-10-28 Potential Defence Mechanisms Triggered by Monosodium Glutamate Sub-Chronic Consumption in Two-Year-Old Wistar Rats Moldovan, Octavia-Laura Vari, Camil-Eugen Tero-Vescan, Amelia Cotoi, Ovidiu Simion Cocuz, Iuliu Gabriel Tabaran, Flaviu Alexandru Pop, Romelia Fülöp, Ibolya Chis, Rafael Florin Lungu, Ioana-Andreea Rusu, Aura Nutrients Article Monosodium glutamate (MSG) is the sodium salt of glutamic acid (GLA), used as a flavour enhancer. MSG is considered a controversial substance. It is incriminated in disturbing the antioxidant system, but also has beneficial effects, as GLA metabolism plays a crucial role in homeostasis. This study highlights which positive or negative aspects of MSG sub-chronic consumption are better reflected in subjects potentially affected by advanced age. Daily doses of MSG were administered to four groups of two-year-old Wistar rats for 90 days: (I) 185 mg/kg bw, (II) 1500 mg/kg bw, (III) 3000 mg/kg bw and (IV) 6000 mg/kg bw, compared to a MSG non-consumer group. Aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase, direct and total bilirubin, total cholesterol, triglycerides, creatinine and urea levels were analysed; stomach, liver and kidney samples were subjected to histopathological analysis. Although, in most cases, there were no statistical differences, interesting aspects of the dose–effect relationship were observed. After MSG sub-chronic consumption, the positive aspects of GLA seem to be reflected better than the negative ones. The hormesis effect, with low-level reactive oxygen species’ protective effects and GLA metabolism, may represent the hypothesis of a potential defence mechanism triggered by MSG sub-chronic consumption in ageing rats. MDPI 2023-10-19 /pmc/articles/PMC10610236/ /pubmed/37892513 http://dx.doi.org/10.3390/nu15204436 Text en © 2023 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
Moldovan, Octavia-Laura
Vari, Camil-Eugen
Tero-Vescan, Amelia
Cotoi, Ovidiu Simion
Cocuz, Iuliu Gabriel
Tabaran, Flaviu Alexandru
Pop, Romelia
Fülöp, Ibolya
Chis, Rafael Florin
Lungu, Ioana-Andreea
Rusu, Aura
Potential Defence Mechanisms Triggered by Monosodium Glutamate Sub-Chronic Consumption in Two-Year-Old Wistar Rats
title Potential Defence Mechanisms Triggered by Monosodium Glutamate Sub-Chronic Consumption in Two-Year-Old Wistar Rats
title_full Potential Defence Mechanisms Triggered by Monosodium Glutamate Sub-Chronic Consumption in Two-Year-Old Wistar Rats
title_fullStr Potential Defence Mechanisms Triggered by Monosodium Glutamate Sub-Chronic Consumption in Two-Year-Old Wistar Rats
title_full_unstemmed Potential Defence Mechanisms Triggered by Monosodium Glutamate Sub-Chronic Consumption in Two-Year-Old Wistar Rats
title_short Potential Defence Mechanisms Triggered by Monosodium Glutamate Sub-Chronic Consumption in Two-Year-Old Wistar Rats
title_sort potential defence mechanisms triggered by monosodium glutamate sub-chronic consumption in two-year-old wistar rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10610236/
https://www.ncbi.nlm.nih.gov/pubmed/37892513
http://dx.doi.org/10.3390/nu15204436
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