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Redox homeostasis of albumin in relation to alpha-lipoic acid and dihydrolipoic acid

Albumin represents the predominant circulating antioxidant agent in plasma exposed to continuous oxidative stress and a change in serum albumin structure accounts for its antioxidant properties. Alterations in the redox status of albumin may result in impairments of its biological properties. Alpha-...

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Autores principales: Atukeren, Pinar, Aydin, Seval, Uslu, Ezel, Gumustas, MKoray, Cakatay, Ufuk
Formato: Texto
Lenguaje:English
Publicado: Landes Bioscience 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2952079/
https://www.ncbi.nlm.nih.gov/pubmed/20716945
http://dx.doi.org/10.4161/oxim.3.3.6
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author Atukeren, Pinar
Aydin, Seval
Uslu, Ezel
Gumustas, MKoray
Cakatay, Ufuk
author_facet Atukeren, Pinar
Aydin, Seval
Uslu, Ezel
Gumustas, MKoray
Cakatay, Ufuk
author_sort Atukeren, Pinar
collection PubMed
description Albumin represents the predominant circulating antioxidant agent in plasma exposed to continuous oxidative stress and a change in serum albumin structure accounts for its antioxidant properties. Alterations in the redox status of albumin may result in impairments of its biological properties. Alpha-lipoic acid (LA), a naturally occurring thiol compound found in virtually all species, is a potent antioxidant with high efficacy which is also involved in the chelation of metal ions, regeneration of antioxidants, and repair of oxidatively damaged proteins. In human body LA is rapidly reduced to dihydrolipoic acid (DHLA) after intake into the cell. Both, LA and DHLA are amphipathic molecules which act as antioxidants both in hydrophilic and lipophilic environments. The present study aimed to investigate the antioxidant/pro-oxidant effects of LA and DHLA due to their concentrations in metal-catalyzed protein oxidation (MCO) of human serum albumin (HSA). Progressive oxidative modification of albumin was found in MCO system by an increased content of protein hydroperoxides (POOH), protein carbonyl groups (PCO) which is the former's major breakdown product, and other protein oxidation markers such as advanced oxidized protein products (AOPP) and protein thiol groups (P-SH). The possible antioxidant protective effects of LA and DHLA were observed with 25 µM and 50 µM; DHLA being more influential. Protein oxidation parameters were found to be lower and P-SH levels seemed higher. However, prooxidant effects of both LA and DHLA came on the scene with increased concentrations of 75 µM and 100 µM where the latter seemed the most hazardous with contradicted results. It is clear that the loss of biological activity of human serum albumin by MCO system appears of medical relevance and if LA exerts similar effects seen in the present study, it is possible that cellular prooxidant activity can also result consuming this unique antioxidant in certain doses.
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spelling pubmed-29520792011-04-25 Redox homeostasis of albumin in relation to alpha-lipoic acid and dihydrolipoic acid Atukeren, Pinar Aydin, Seval Uslu, Ezel Gumustas, MKoray Cakatay, Ufuk Oxid Med Cell Longev Research Papers Albumin represents the predominant circulating antioxidant agent in plasma exposed to continuous oxidative stress and a change in serum albumin structure accounts for its antioxidant properties. Alterations in the redox status of albumin may result in impairments of its biological properties. Alpha-lipoic acid (LA), a naturally occurring thiol compound found in virtually all species, is a potent antioxidant with high efficacy which is also involved in the chelation of metal ions, regeneration of antioxidants, and repair of oxidatively damaged proteins. In human body LA is rapidly reduced to dihydrolipoic acid (DHLA) after intake into the cell. Both, LA and DHLA are amphipathic molecules which act as antioxidants both in hydrophilic and lipophilic environments. The present study aimed to investigate the antioxidant/pro-oxidant effects of LA and DHLA due to their concentrations in metal-catalyzed protein oxidation (MCO) of human serum albumin (HSA). Progressive oxidative modification of albumin was found in MCO system by an increased content of protein hydroperoxides (POOH), protein carbonyl groups (PCO) which is the former's major breakdown product, and other protein oxidation markers such as advanced oxidized protein products (AOPP) and protein thiol groups (P-SH). The possible antioxidant protective effects of LA and DHLA were observed with 25 µM and 50 µM; DHLA being more influential. Protein oxidation parameters were found to be lower and P-SH levels seemed higher. However, prooxidant effects of both LA and DHLA came on the scene with increased concentrations of 75 µM and 100 µM where the latter seemed the most hazardous with contradicted results. It is clear that the loss of biological activity of human serum albumin by MCO system appears of medical relevance and if LA exerts similar effects seen in the present study, it is possible that cellular prooxidant activity can also result consuming this unique antioxidant in certain doses. Landes Bioscience 2010 /pmc/articles/PMC2952079/ /pubmed/20716945 http://dx.doi.org/10.4161/oxim.3.3.6 Text en Copyright © 2010 Landes Bioscience
spellingShingle Research Papers
Atukeren, Pinar
Aydin, Seval
Uslu, Ezel
Gumustas, MKoray
Cakatay, Ufuk
Redox homeostasis of albumin in relation to alpha-lipoic acid and dihydrolipoic acid
title Redox homeostasis of albumin in relation to alpha-lipoic acid and dihydrolipoic acid
title_full Redox homeostasis of albumin in relation to alpha-lipoic acid and dihydrolipoic acid
title_fullStr Redox homeostasis of albumin in relation to alpha-lipoic acid and dihydrolipoic acid
title_full_unstemmed Redox homeostasis of albumin in relation to alpha-lipoic acid and dihydrolipoic acid
title_short Redox homeostasis of albumin in relation to alpha-lipoic acid and dihydrolipoic acid
title_sort redox homeostasis of albumin in relation to alpha-lipoic acid and dihydrolipoic acid
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2952079/
https://www.ncbi.nlm.nih.gov/pubmed/20716945
http://dx.doi.org/10.4161/oxim.3.3.6
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