<i>Ishige okamurae</i> Ameliorates Methylglyoxal-Induced Nephrotoxicity via Reducing Oxidative Stress, RAGE Protein Expression, and Modulating MAPK, Nrf2/ARE Signaling Pathway in Mouse Glomerular Mesangial Cells

Advanced glycation end-products (AGEs) such as methylglyoxal (MGO) play a vital role in the pathogenesis of nephropathy, a diabetic complication. In the present study, we evaluated the anti-glycation and renal protective properties of <i>Ishige okamurae</i> extract (IOE) against AGE-indu...

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Main Authors: Mingyeong Kim, Chiheung Cho, Changjun Lee, Bomi Ryu, Sera Kim, Jinyoung Hur, Sang-Hoon Lee
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:Foods
Subjects:
Online Access:https://www.mdpi.com/2304-8158/10/9/2000
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author Mingyeong Kim
Chiheung Cho
Changjun Lee
Bomi Ryu
Sera Kim
Jinyoung Hur
Sang-Hoon Lee
author_facet Mingyeong Kim
Chiheung Cho
Changjun Lee
Bomi Ryu
Sera Kim
Jinyoung Hur
Sang-Hoon Lee
author_sort Mingyeong Kim
collection DOAJ
description Advanced glycation end-products (AGEs) such as methylglyoxal (MGO) play a vital role in the pathogenesis of nephropathy, a diabetic complication. In the present study, we evaluated the anti-glycation and renal protective properties of <i>Ishige okamurae</i> extract (IOE) against AGE-induced oxidative stress. HPLC analysis confirmed that bioactive phlorotannins such as diphlorethohydroxycarmalol and ishophloroglucin A are predominantly present in IOE. IOE showed strong anti-glycation activities via inhibition of AGE formation, inhibition of AGE–protein cross-linking, and breaking of AGE–protein cross-links. In addition, in vitro studies using mesangial cells demonstrated that IOE effectively suppressed intracellular reactive oxygen species production, intracellular MGO accumulation, and apoptotic cell death by MGO-induced oxidative stress, in addition to regulating the expression of proteins involved in the receptor for AGEs and nuclear factor erythroid 2-related factor 2 (Nrf2)/antioxidant response elements (ARE) signaling pathways. Therefore, IOE can serve as a natural therapeutic agent for the management of AGE-related nephropathy.
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spelling doaj.art-9c41bed11421473daa6909bf266f473d2023-11-22T13:02:41ZengMDPI AGFoods2304-81582021-08-01109200010.3390/foods10092000<i>Ishige okamurae</i> Ameliorates Methylglyoxal-Induced Nephrotoxicity via Reducing Oxidative Stress, RAGE Protein Expression, and Modulating MAPK, Nrf2/ARE Signaling Pathway in Mouse Glomerular Mesangial CellsMingyeong Kim0Chiheung Cho1Changjun Lee2Bomi Ryu3Sera Kim4Jinyoung Hur5Sang-Hoon Lee6Department of Food Biotechnology, University of Science and Technology, Daejeon 34113, KoreaDivision of Functional Food Research, Korea Food Research Institute, 245 Nongsaengmyeong-ro, Iseo-myeon, Wanju-gun 55365, KoreaDivision of Functional Food Research, Korea Food Research Institute, 245 Nongsaengmyeong-ro, Iseo-myeon, Wanju-gun 55365, KoreaMarine Science Institute, Jeju National University, Jeju 63333, KoreaDivision of Functional Food Research, Korea Food Research Institute, 245 Nongsaengmyeong-ro, Iseo-myeon, Wanju-gun 55365, KoreaDivision of Functional Food Research, Korea Food Research Institute, 245 Nongsaengmyeong-ro, Iseo-myeon, Wanju-gun 55365, KoreaDepartment of Food Biotechnology, University of Science and Technology, Daejeon 34113, KoreaAdvanced glycation end-products (AGEs) such as methylglyoxal (MGO) play a vital role in the pathogenesis of nephropathy, a diabetic complication. In the present study, we evaluated the anti-glycation and renal protective properties of <i>Ishige okamurae</i> extract (IOE) against AGE-induced oxidative stress. HPLC analysis confirmed that bioactive phlorotannins such as diphlorethohydroxycarmalol and ishophloroglucin A are predominantly present in IOE. IOE showed strong anti-glycation activities via inhibition of AGE formation, inhibition of AGE–protein cross-linking, and breaking of AGE–protein cross-links. In addition, in vitro studies using mesangial cells demonstrated that IOE effectively suppressed intracellular reactive oxygen species production, intracellular MGO accumulation, and apoptotic cell death by MGO-induced oxidative stress, in addition to regulating the expression of proteins involved in the receptor for AGEs and nuclear factor erythroid 2-related factor 2 (Nrf2)/antioxidant response elements (ARE) signaling pathways. Therefore, IOE can serve as a natural therapeutic agent for the management of AGE-related nephropathy.https://www.mdpi.com/2304-8158/10/9/2000<i>Ishige okamurae</i>advanced glycation end-productnephropathymethylglyoxalNrf2/ARE pathway
spellingShingle Mingyeong Kim
Chiheung Cho
Changjun Lee
Bomi Ryu
Sera Kim
Jinyoung Hur
Sang-Hoon Lee
<i>Ishige okamurae</i> Ameliorates Methylglyoxal-Induced Nephrotoxicity via Reducing Oxidative Stress, RAGE Protein Expression, and Modulating MAPK, Nrf2/ARE Signaling Pathway in Mouse Glomerular Mesangial Cells
Foods
<i>Ishige okamurae</i>
advanced glycation end-product
nephropathy
methylglyoxal
Nrf2/ARE pathway
title <i>Ishige okamurae</i> Ameliorates Methylglyoxal-Induced Nephrotoxicity via Reducing Oxidative Stress, RAGE Protein Expression, and Modulating MAPK, Nrf2/ARE Signaling Pathway in Mouse Glomerular Mesangial Cells
title_full <i>Ishige okamurae</i> Ameliorates Methylglyoxal-Induced Nephrotoxicity via Reducing Oxidative Stress, RAGE Protein Expression, and Modulating MAPK, Nrf2/ARE Signaling Pathway in Mouse Glomerular Mesangial Cells
title_fullStr <i>Ishige okamurae</i> Ameliorates Methylglyoxal-Induced Nephrotoxicity via Reducing Oxidative Stress, RAGE Protein Expression, and Modulating MAPK, Nrf2/ARE Signaling Pathway in Mouse Glomerular Mesangial Cells
title_full_unstemmed <i>Ishige okamurae</i> Ameliorates Methylglyoxal-Induced Nephrotoxicity via Reducing Oxidative Stress, RAGE Protein Expression, and Modulating MAPK, Nrf2/ARE Signaling Pathway in Mouse Glomerular Mesangial Cells
title_short <i>Ishige okamurae</i> Ameliorates Methylglyoxal-Induced Nephrotoxicity via Reducing Oxidative Stress, RAGE Protein Expression, and Modulating MAPK, Nrf2/ARE Signaling Pathway in Mouse Glomerular Mesangial Cells
title_sort i ishige okamurae i ameliorates methylglyoxal induced nephrotoxicity via reducing oxidative stress rage protein expression and modulating mapk nrf2 are signaling pathway in mouse glomerular mesangial cells
topic <i>Ishige okamurae</i>
advanced glycation end-product
nephropathy
methylglyoxal
Nrf2/ARE pathway
url https://www.mdpi.com/2304-8158/10/9/2000
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