Protective Effect of Liposome-Encapsulated Glutathione in a Human Epidermal Model Exposed to a Mustard Gas Analog

Sulfur mustard or mustard gas (HD) and its monofunctional analog, 2-chloroethyl ethyl sulfide (CEES), or “half-mustard gas,” are alkylating agents that induce DNA damage, oxidative stress, and inflammation. HD/CEES are rapidly absorbed in the skin causing extensive injury. We hypothesize that antiox...

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Main Authors: Victor Paromov, Sudha Kumari, Marianne Brannon, Naga S. Kanaparthy, Hongsong Yang, Milton G. Smith, William L. Stone
Format: Article
Language:English
Published: Wiley 2011-01-01
Series:Journal of Toxicology
Online Access:http://dx.doi.org/10.1155/2011/109516
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author Victor Paromov
Sudha Kumari
Marianne Brannon
Naga S. Kanaparthy
Hongsong Yang
Milton G. Smith
William L. Stone
author_facet Victor Paromov
Sudha Kumari
Marianne Brannon
Naga S. Kanaparthy
Hongsong Yang
Milton G. Smith
William L. Stone
author_sort Victor Paromov
collection DOAJ
description Sulfur mustard or mustard gas (HD) and its monofunctional analog, 2-chloroethyl ethyl sulfide (CEES), or “half-mustard gas,” are alkylating agents that induce DNA damage, oxidative stress, and inflammation. HD/CEES are rapidly absorbed in the skin causing extensive injury. We hypothesize that antioxidant liposomes that deliver both water-soluble and lipid-soluble antioxidants protect skin cells from immediate CEES-induced damage via attenuating oxidative stress. Liposomes containing water-soluble antioxidants and/or lipid-soluble antioxidants were evaluated using in vitro model systems. Initially, we found that liposomes containing encapsulated glutathione (GSH-liposomes) increased cell viability and attenuated production of reactive oxygen species (ROS) in HaCaT cells exposed to CEES. Next, GSH-liposomes were tested in a human epidermal model, EpiDerm. In the EpiDerm, GSH-liposomes administered simultaneously or 1 hour after CEES exposure (2.5 mM) increased cell viability, inhibited CEES-induced loss of ATP and attenuated changes in cellular morphology, but did not reduce caspase-3 activity. These findings paralleled the previously described in vivo protective effect of antioxidant liposomes in the rat lung and established the effectiveness of GSH-liposomes in a human epidermal model. This study provides a rationale for use of antioxidant liposomes against HD toxicity in the skin considering further verification in animal models exposed to HD.
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institution Kabale University
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spelling doaj-art-339bf1496784486aa23854c037f6f16e2025-02-03T05:50:19ZengWileyJournal of Toxicology1687-81911687-82052011-01-01201110.1155/2011/109516109516Protective Effect of Liposome-Encapsulated Glutathione in a Human Epidermal Model Exposed to a Mustard Gas AnalogVictor Paromov0Sudha Kumari1Marianne Brannon2Naga S. Kanaparthy3Hongsong Yang4Milton G. Smith5William L. Stone6Department of Pharmacology, Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37614, USADepartment of Pediatrics, Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37614, USADepartment of Pediatrics, Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37614, USADepartment of Pediatrics, Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37614, USADepartment of Pediatrics, Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37614, USAAmaox, Ltd., 6300 N. Wickham Road 208, Melbourne, FL, USADepartment of Pediatrics, Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37614, USASulfur mustard or mustard gas (HD) and its monofunctional analog, 2-chloroethyl ethyl sulfide (CEES), or “half-mustard gas,” are alkylating agents that induce DNA damage, oxidative stress, and inflammation. HD/CEES are rapidly absorbed in the skin causing extensive injury. We hypothesize that antioxidant liposomes that deliver both water-soluble and lipid-soluble antioxidants protect skin cells from immediate CEES-induced damage via attenuating oxidative stress. Liposomes containing water-soluble antioxidants and/or lipid-soluble antioxidants were evaluated using in vitro model systems. Initially, we found that liposomes containing encapsulated glutathione (GSH-liposomes) increased cell viability and attenuated production of reactive oxygen species (ROS) in HaCaT cells exposed to CEES. Next, GSH-liposomes were tested in a human epidermal model, EpiDerm. In the EpiDerm, GSH-liposomes administered simultaneously or 1 hour after CEES exposure (2.5 mM) increased cell viability, inhibited CEES-induced loss of ATP and attenuated changes in cellular morphology, but did not reduce caspase-3 activity. These findings paralleled the previously described in vivo protective effect of antioxidant liposomes in the rat lung and established the effectiveness of GSH-liposomes in a human epidermal model. This study provides a rationale for use of antioxidant liposomes against HD toxicity in the skin considering further verification in animal models exposed to HD.http://dx.doi.org/10.1155/2011/109516
spellingShingle Victor Paromov
Sudha Kumari
Marianne Brannon
Naga S. Kanaparthy
Hongsong Yang
Milton G. Smith
William L. Stone
Protective Effect of Liposome-Encapsulated Glutathione in a Human Epidermal Model Exposed to a Mustard Gas Analog
Journal of Toxicology
title Protective Effect of Liposome-Encapsulated Glutathione in a Human Epidermal Model Exposed to a Mustard Gas Analog
title_full Protective Effect of Liposome-Encapsulated Glutathione in a Human Epidermal Model Exposed to a Mustard Gas Analog
title_fullStr Protective Effect of Liposome-Encapsulated Glutathione in a Human Epidermal Model Exposed to a Mustard Gas Analog
title_full_unstemmed Protective Effect of Liposome-Encapsulated Glutathione in a Human Epidermal Model Exposed to a Mustard Gas Analog
title_short Protective Effect of Liposome-Encapsulated Glutathione in a Human Epidermal Model Exposed to a Mustard Gas Analog
title_sort protective effect of liposome encapsulated glutathione in a human epidermal model exposed to a mustard gas analog
url http://dx.doi.org/10.1155/2011/109516
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