Effect of grape seed extract on the oxidative and proliferative status of porcine intestinal epithelial cells

The aim of this study was to investigate the oxidative and proliferative effects of grape seed extract (GSE). Piglet intestinal epithelial cells (IPEC1) were selected as an unstressed cell model, or they were exposed to 400 μM H2O2 to establish a H2O2-stimulated cell model. The glutathione (GSH) and...

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Main Authors: Jinhe KANG, Tan YANG, Zhaoliang WU, Jing YANG, Min XIONG, Zhiliang TAN, Zhihong SUN, Wenjun XIAO
Format: Article
Language:English
Published: Kafkas University, Faculty of Veterinary Medicine 2018-05-01
Series:Kafkas Universitesi Veteriner Fakültesi Dergisi
Subjects:
Online Access:https://vetdergikafkas.org/pdf.php?id=2369
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author Jinhe KANG
Tan YANG
Zhaoliang WU
Jing YANG
Min XIONG
Zhiliang TAN
Zhihong SUN
Wenjun XIAO
author_facet Jinhe KANG
Tan YANG
Zhaoliang WU
Jing YANG
Min XIONG
Zhiliang TAN
Zhihong SUN
Wenjun XIAO
author_sort Jinhe KANG
collection DOAJ
description The aim of this study was to investigate the oxidative and proliferative effects of grape seed extract (GSE). Piglet intestinal epithelial cells (IPEC1) were selected as an unstressed cell model, or they were exposed to 400 μM H2O2 to establish a H2O2-stimulated cell model. The glutathione (GSH) and total antioxidant capacity in response to GSE addition were tested in the unstressed and H2O2-stimulated cell models. The relative mRNA levels of antioxidant or antioxidant enzymes and apoptosis-related genes were measured by Real-Time RT-PCR. In the unstressed status, the cell survival ratio and GSH increased with the addition of GSE at 1 and 10 μg/mL but diminished at 60 μg GSE/mL. The addition of 1 μg/mL GSE upregulated the mRNA expression levels of B-Cell Lymphoma protein-2 (Bcl-2), cysteine aspartases-3 (Caspase-3), cysteine aspartases-8 (Caspase-8) and glutathione peroxidase-1(GPx-1), while it downregulated that of Bcl2-associated X protein (Bax), copper-zinc superoxide dismutase, glutathione S-transferase (GST), thioredoxin, thioltransferase and thioredoxin reductase. As GSE reached 60 μg/mL, the tumor protein p53 (p53) and caspase-8 gene expressions were upregulated. In stressed status, 1 and 10 μg GSE/mL promoted the increase of GSH. H2O2- induced increases in Bax, p53, and Caspase-3 mRNA expressions were attenuated by the subsequent addition of 1 μg GSE/mL and promoted the gene expression of tumor necrosis factor-α, GPx-1 and thioltransferase (Ttas). Treatment with 60 μg GSE/ml resulted in a significant reduction in Bax, p53, manganese superoxide dismutase and GST mRNA expressions. These results indicate that GSE exhibits antioxidative and proliferative functions on unstressed IPEC1 cells at low and medium levels and oxidative and antiproliferative functions at high levels.
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spelling doaj.art-de697f954b1e4bb2b20ca749088e9e0a2023-06-19T06:41:24ZengKafkas University, Faculty of Veterinary MedicineKafkas Universitesi Veteriner Fakültesi Dergisi1309-22512018-05-0124451151710.9775/kvfd.2018.194572369Effect of grape seed extract on the oxidative and proliferative status of porcine intestinal epithelial cellsJinhe KANG0Tan YANG1Zhaoliang WU2Jing YANG3Min XIONG4Zhiliang TAN5Zhihong SUN6Wenjun XIAO7Key Laboratory of Agro-ecological Processes in Subtropical Region, Hunan Research Center of Livestock & Poultry, Sciences, South-Central Experimental Station of Animal Nutrition and Feed Science in Ministry of Agriculture, Institute of Subtropical Agriculture, The Chinese Academy of Sciences, Changsha, Hunan 410125, P. R. CHINAKey Laboratory of Agro-ecological Processes in Subtropical Region, Hunan Research Center of Livestock & Poultry, Sciences, South-Central Experimental Station of Animal Nutrition and Feed Science in Ministry of Agriculture, Institute of Subtropical Agriculture, The Chinese Academy of Sciences, Changsha, Hunan 410125, P. R. CHINAKey Laboratory for Bio-feed and Molecular Nutrition, Southwest University, Chongqing 400715, P. R. CHINAKey Laboratory for Bio-feed and Molecular Nutrition, Southwest University, Chongqing 400715, P. R. CHINAKey Laboratory for Bio-feed and Molecular Nutrition, Southwest University, Chongqing 400715, P. R. CHINAKey Laboratory of Agro-ecological Processes in Subtropical Region, Hunan Research Center of Livestock & Poultry, Sciences, South-Central Experimental Station of Animal Nutrition and Feed Science in Ministry of Agriculture, Institute of Subtropical Agriculture, The Chinese Academy of Sciences, Changsha, Hunan 410125, P. R. CHINAKey Laboratory for Bio-feed and Molecular Nutrition, Southwest University, Chongqing 400715, P. R. CHINANational Research Center of Engineering & Technology for Utilization of Botanical Functional Ingredients, Hunan Agricultural University, Changsha, Hunan 410128, P. R. CHINAThe aim of this study was to investigate the oxidative and proliferative effects of grape seed extract (GSE). Piglet intestinal epithelial cells (IPEC1) were selected as an unstressed cell model, or they were exposed to 400 μM H2O2 to establish a H2O2-stimulated cell model. The glutathione (GSH) and total antioxidant capacity in response to GSE addition were tested in the unstressed and H2O2-stimulated cell models. The relative mRNA levels of antioxidant or antioxidant enzymes and apoptosis-related genes were measured by Real-Time RT-PCR. In the unstressed status, the cell survival ratio and GSH increased with the addition of GSE at 1 and 10 μg/mL but diminished at 60 μg GSE/mL. The addition of 1 μg/mL GSE upregulated the mRNA expression levels of B-Cell Lymphoma protein-2 (Bcl-2), cysteine aspartases-3 (Caspase-3), cysteine aspartases-8 (Caspase-8) and glutathione peroxidase-1(GPx-1), while it downregulated that of Bcl2-associated X protein (Bax), copper-zinc superoxide dismutase, glutathione S-transferase (GST), thioredoxin, thioltransferase and thioredoxin reductase. As GSE reached 60 μg/mL, the tumor protein p53 (p53) and caspase-8 gene expressions were upregulated. In stressed status, 1 and 10 μg GSE/mL promoted the increase of GSH. H2O2- induced increases in Bax, p53, and Caspase-3 mRNA expressions were attenuated by the subsequent addition of 1 μg GSE/mL and promoted the gene expression of tumor necrosis factor-α, GPx-1 and thioltransferase (Ttas). Treatment with 60 μg GSE/ml resulted in a significant reduction in Bax, p53, manganese superoxide dismutase and GST mRNA expressions. These results indicate that GSE exhibits antioxidative and proliferative functions on unstressed IPEC1 cells at low and medium levels and oxidative and antiproliferative functions at high levels.https://vetdergikafkas.org/pdf.php?id=2369grape seed extractantioxidationproliferationintestinal epithelial cells
spellingShingle Jinhe KANG
Tan YANG
Zhaoliang WU
Jing YANG
Min XIONG
Zhiliang TAN
Zhihong SUN
Wenjun XIAO
Effect of grape seed extract on the oxidative and proliferative status of porcine intestinal epithelial cells
Kafkas Universitesi Veteriner Fakültesi Dergisi
grape seed extract
antioxidation
proliferation
intestinal epithelial cells
title Effect of grape seed extract on the oxidative and proliferative status of porcine intestinal epithelial cells
title_full Effect of grape seed extract on the oxidative and proliferative status of porcine intestinal epithelial cells
title_fullStr Effect of grape seed extract on the oxidative and proliferative status of porcine intestinal epithelial cells
title_full_unstemmed Effect of grape seed extract on the oxidative and proliferative status of porcine intestinal epithelial cells
title_short Effect of grape seed extract on the oxidative and proliferative status of porcine intestinal epithelial cells
title_sort effect of grape seed extract on the oxidative and proliferative status of porcine intestinal epithelial cells
topic grape seed extract
antioxidation
proliferation
intestinal epithelial cells
url https://vetdergikafkas.org/pdf.php?id=2369
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