RAGE-Dependent Effect of Exogenous Methylglyoxal Intake on Lung Biomechanics in Mice

Methylglyoxal (MG) is a known highly reactive dicarbonyl and precursor to free radicals and advanced glycation end-products (AGEs). It is discussed to be involved in tissue aging and in the pathogenesis of different degenerative diseases. The effect of long-term oral administration of MG, simulating...

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Main Authors: Samiya Al-Robaiy, Alexander Navarrete Santos, Andreas Simm
Format: Article
Language:English
Published: MDPI AG 2022-12-01
Series:Nutrients
Subjects:
Online Access:https://www.mdpi.com/2072-6643/15/1/23
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author Samiya Al-Robaiy
Alexander Navarrete Santos
Andreas Simm
author_facet Samiya Al-Robaiy
Alexander Navarrete Santos
Andreas Simm
author_sort Samiya Al-Robaiy
collection DOAJ
description Methylglyoxal (MG) is a known highly reactive dicarbonyl and precursor to free radicals and advanced glycation end-products (AGEs). It is discussed to be involved in tissue aging and in the pathogenesis of different degenerative diseases. The effect of long-term oral administration of MG, simulating dietary MG intake, on the lung biomechanics of wild type (WT) and receptor for advanced glycation end-products knockout (RAGE-KO) mice was studied using an ex vivo ventilation system starting at the age of 6 months and after feeding for 6 and 12 months with MG. Our results showed that MG was taken up in the circulation and efficiently excreted with urine. The amount of free urinary MG measured after 12 months of feeding was lowered. After 12 months feeding, a significant airway resistance increase accompanied by a decrease of the maximal inspiratory airflow was observed in WT animals. No effect of MG in lung function of RAGE-KO mice could be detected. Despite the evidence that MG entered the systemic circulation, no MG-derived AGE accumulation was detected in the lung lysates in dependency on MG-feeding. Our data indicate that the short-term feeding of MG has little effect in vivo. Only after long-term treatment was MG secretion reduced, leading to tissue impairment.
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spelling doaj.art-5925a4adc9404e3caa29a99ae239da4d2023-12-02T00:45:27ZengMDPI AGNutrients2072-66432022-12-011512310.3390/nu15010023RAGE-Dependent Effect of Exogenous Methylglyoxal Intake on Lung Biomechanics in MiceSamiya Al-Robaiy0Alexander Navarrete Santos1Andreas Simm2Center for Basic Medical Research (ZMG), University Hospital Halle (Saale), Martin Luther University Halle-Wittenberg, 06108 Halle (Saale), GermanyCenter for Basic Medical Research (ZMG), University Hospital Halle (Saale), Martin Luther University Halle-Wittenberg, 06108 Halle (Saale), GermanyCenter for Basic Medical Research (ZMG), University Hospital Halle (Saale), Martin Luther University Halle-Wittenberg, 06108 Halle (Saale), GermanyMethylglyoxal (MG) is a known highly reactive dicarbonyl and precursor to free radicals and advanced glycation end-products (AGEs). It is discussed to be involved in tissue aging and in the pathogenesis of different degenerative diseases. The effect of long-term oral administration of MG, simulating dietary MG intake, on the lung biomechanics of wild type (WT) and receptor for advanced glycation end-products knockout (RAGE-KO) mice was studied using an ex vivo ventilation system starting at the age of 6 months and after feeding for 6 and 12 months with MG. Our results showed that MG was taken up in the circulation and efficiently excreted with urine. The amount of free urinary MG measured after 12 months of feeding was lowered. After 12 months feeding, a significant airway resistance increase accompanied by a decrease of the maximal inspiratory airflow was observed in WT animals. No effect of MG in lung function of RAGE-KO mice could be detected. Despite the evidence that MG entered the systemic circulation, no MG-derived AGE accumulation was detected in the lung lysates in dependency on MG-feeding. Our data indicate that the short-term feeding of MG has little effect in vivo. Only after long-term treatment was MG secretion reduced, leading to tissue impairment.https://www.mdpi.com/2072-6643/15/1/23methylglyoxallung biomechanicsreceptor for advanced glycation end-productsex vivo ventilation
spellingShingle Samiya Al-Robaiy
Alexander Navarrete Santos
Andreas Simm
RAGE-Dependent Effect of Exogenous Methylglyoxal Intake on Lung Biomechanics in Mice
Nutrients
methylglyoxal
lung biomechanics
receptor for advanced glycation end-products
ex vivo ventilation
title RAGE-Dependent Effect of Exogenous Methylglyoxal Intake on Lung Biomechanics in Mice
title_full RAGE-Dependent Effect of Exogenous Methylglyoxal Intake on Lung Biomechanics in Mice
title_fullStr RAGE-Dependent Effect of Exogenous Methylglyoxal Intake on Lung Biomechanics in Mice
title_full_unstemmed RAGE-Dependent Effect of Exogenous Methylglyoxal Intake on Lung Biomechanics in Mice
title_short RAGE-Dependent Effect of Exogenous Methylglyoxal Intake on Lung Biomechanics in Mice
title_sort rage dependent effect of exogenous methylglyoxal intake on lung biomechanics in mice
topic methylglyoxal
lung biomechanics
receptor for advanced glycation end-products
ex vivo ventilation
url https://www.mdpi.com/2072-6643/15/1/23
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