Curcumin Nanocarriers in the Protection Against Iron- and Alcohol-Induced Oxidative Stress in a Cellular Model of Liver Disease

During chronic alcohol misuse, hepatic iron overload occurs, leading to exacerbated oxidative stress and liver injury. The aim was to study formulations encapsulated with the antioxidant curcumin to assess their ability protect against oxidative stress in a model of alcohol-related liver disease (AL...

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Main Authors: Lucy Petagine, Mohammed G. Zariwala, Satyanarayana Somavarapu, Stefanie Ho Yi Chan, Vinood B. Patel
Format: Article
Language:English
Published: MDPI AG 2025-04-01
Series:Biology
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Online Access:https://www.mdpi.com/2079-7737/14/5/455
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author Lucy Petagine
Mohammed G. Zariwala
Satyanarayana Somavarapu
Stefanie Ho Yi Chan
Vinood B. Patel
author_facet Lucy Petagine
Mohammed G. Zariwala
Satyanarayana Somavarapu
Stefanie Ho Yi Chan
Vinood B. Patel
author_sort Lucy Petagine
collection DOAJ
description During chronic alcohol misuse, hepatic iron overload occurs, leading to exacerbated oxidative stress and liver injury. The aim was to study formulations encapsulated with the antioxidant curcumin to assess their ability protect against oxidative stress in a model of alcohol-related liver disease (ALD) combined with iron. HepG2 (VL-17A) cells were treated with iron (50 µM) alone or with alcohol (200 to 350 mM) over 72 h and markers of oxidative damage, cell death, and mitochondrial function were assessed. Nanoformulations encapsulating curcumin were also studied. VL-17A cells treated with both ethanol and iron showed significant decreases in cell viability (64%, <i>p</i> < 0.0001) when compared to control, and a 56% decrease (<i>p</i> = 0.0279) when compared to iron-only treatment. Iron-alone treatment caused a 115% increase (<i>p</i> < 0.0001) in ROS at 48 h as well as increases of up to 118% when treated with 200 mM ethanol + 50 μM iron (<i>p</i> < 0.0001), compared to control DMEM. The study found that 10 µM curcumin DSPE-PEG increased cell viability by 17% and 41% when compared to control and iron treatment alone, respectively. Formulations reduced ROS by 36% (<i>p</i> = 0.0015) when compared to iron-alone treatment. In summary, encapsulated curcumin provided antioxidant capacity and reduced oxidative stress, demonstrating the therapeutic potential for curcumin formulations in ALD combined with iron dysregulation.
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spelling doaj-art-1208afcf2b28445187d635ceeede78cf2025-08-20T03:14:40ZengMDPI AGBiology2079-77372025-04-0114545510.3390/biology14050455Curcumin Nanocarriers in the Protection Against Iron- and Alcohol-Induced Oxidative Stress in a Cellular Model of Liver DiseaseLucy Petagine0Mohammed G. Zariwala1Satyanarayana Somavarapu2Stefanie Ho Yi Chan3Vinood B. Patel4Centre for Nutraceuticals, School of Life Sciences, University of Westminster, London W1W 6UW, UKCentre for Nutraceuticals, School of Life Sciences, University of Westminster, London W1W 6UW, UKDepartment of Pharmaceutics, UCL School of Pharmacy, London WC1N 1AX, UKCentre for Nutraceuticals, School of Life Sciences, University of Westminster, London W1W 6UW, UKCentre for Nutraceuticals, School of Life Sciences, University of Westminster, London W1W 6UW, UKDuring chronic alcohol misuse, hepatic iron overload occurs, leading to exacerbated oxidative stress and liver injury. The aim was to study formulations encapsulated with the antioxidant curcumin to assess their ability protect against oxidative stress in a model of alcohol-related liver disease (ALD) combined with iron. HepG2 (VL-17A) cells were treated with iron (50 µM) alone or with alcohol (200 to 350 mM) over 72 h and markers of oxidative damage, cell death, and mitochondrial function were assessed. Nanoformulations encapsulating curcumin were also studied. VL-17A cells treated with both ethanol and iron showed significant decreases in cell viability (64%, <i>p</i> < 0.0001) when compared to control, and a 56% decrease (<i>p</i> = 0.0279) when compared to iron-only treatment. Iron-alone treatment caused a 115% increase (<i>p</i> < 0.0001) in ROS at 48 h as well as increases of up to 118% when treated with 200 mM ethanol + 50 μM iron (<i>p</i> < 0.0001), compared to control DMEM. The study found that 10 µM curcumin DSPE-PEG increased cell viability by 17% and 41% when compared to control and iron treatment alone, respectively. Formulations reduced ROS by 36% (<i>p</i> = 0.0015) when compared to iron-alone treatment. In summary, encapsulated curcumin provided antioxidant capacity and reduced oxidative stress, demonstrating the therapeutic potential for curcumin formulations in ALD combined with iron dysregulation.https://www.mdpi.com/2079-7737/14/5/455alcoholantioxidantscurcuminironlivermitochondria
spellingShingle Lucy Petagine
Mohammed G. Zariwala
Satyanarayana Somavarapu
Stefanie Ho Yi Chan
Vinood B. Patel
Curcumin Nanocarriers in the Protection Against Iron- and Alcohol-Induced Oxidative Stress in a Cellular Model of Liver Disease
Biology
alcohol
antioxidants
curcumin
iron
liver
mitochondria
title Curcumin Nanocarriers in the Protection Against Iron- and Alcohol-Induced Oxidative Stress in a Cellular Model of Liver Disease
title_full Curcumin Nanocarriers in the Protection Against Iron- and Alcohol-Induced Oxidative Stress in a Cellular Model of Liver Disease
title_fullStr Curcumin Nanocarriers in the Protection Against Iron- and Alcohol-Induced Oxidative Stress in a Cellular Model of Liver Disease
title_full_unstemmed Curcumin Nanocarriers in the Protection Against Iron- and Alcohol-Induced Oxidative Stress in a Cellular Model of Liver Disease
title_short Curcumin Nanocarriers in the Protection Against Iron- and Alcohol-Induced Oxidative Stress in a Cellular Model of Liver Disease
title_sort curcumin nanocarriers in the protection against iron and alcohol induced oxidative stress in a cellular model of liver disease
topic alcohol
antioxidants
curcumin
iron
liver
mitochondria
url https://www.mdpi.com/2079-7737/14/5/455
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