Literature DB >> 12509339

Antioxidants, oxidative damage and oxygen deprivation stress: a review.

Olga Blokhina1, Eija Virolainen, Kurt V Fagerstedt.   

Abstract

Oxidative stress is induced by a wide range of environmental factors including UV stress, pathogen invasion (hypersensitive reaction), herbicide action and oxygen shortage. Oxygen deprivation stress in plant cells is distinguished by three physiologically different states: transient hypoxia, anoxia and reoxygenation. Generation of reactive oxygen species (ROS) is characteristic for hypoxia and especially for reoxygenation. Of the ROS, hydrogen peroxide (H(2)O(2)) and superoxide (O(2)(.-)) are both produced in a number of cellular reactions, including the iron-catalysed Fenton reaction, and by various enzymes such as lipoxygenases, peroxidases, NADPH oxidase and xanthine oxidase. The main cellular components susceptible to damage by free radicals are lipids (peroxidation of unsaturated fatty acids in membranes), proteins (denaturation), carbohydrates and nucleic acids. Consequences of hypoxia-induced oxidative stress depend on tissue and/or species (i.e. their tolerance to anoxia), on membrane properties, on endogenous antioxidant content and on the ability to induce the response in the antioxidant system. Effective utilization of energy resources (starch, sugars) and the switch to anaerobic metabolism and the preservation of the redox status of the cell are vital for survival. The formation of ROS is prevented by an antioxidant system: low molecular mass antioxidants (ascorbic acid, glutathione, tocopherols), enzymes regenerating the reduced forms of antioxidants, and ROS-interacting enzymes such as SOD, peroxidases and catalases. In plant tissues many phenolic compounds (in addition to tocopherols) are potential antioxidants: flavonoids, tannins and lignin precursors may work as ROS-scavenging compounds. Antioxidants act as a cooperative network, employing a series of redox reactions. Interactions between ascorbic acid and glutathione, and ascorbic acid and phenolic compounds are well known. Under oxygen deprivation stress some contradictory results on the antioxidant status have been obtained. Experiments on overexpression of antioxidant production do not always result in the enhancement of the antioxidative defence, and hence increased antioxidative capacity does not always correlate positively with the degree of protection. Here we present a consideration of factors which possibly affect the effectiveness of antioxidant protection under oxygen deprivation as well as under other environmental stresses. Such aspects as compartmentalization of ROS formation and antioxidant localization, synthesis and transport of antioxidants, the ability to induce the antioxidant defense and cooperation (and/or compensation) between different antioxidant systems are the determinants of the competence of the antioxidant system.

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Year:  2003        PMID: 12509339      PMCID: PMC4244988          DOI: 10.1093/aob/mcf118

Source DB:  PubMed          Journal:  Ann Bot        ISSN: 0305-7364            Impact factor:   4.357


  77 in total

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2.  Modulation of liposomal membrane fluidity by flavonoids and isoflavonoids.

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3.  Changes in carotenoids, tocopherols and diterpenes during drought and recovery, and the biological significance of chlorophyll loss in Rosmarinus officinalis plants.

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4.  Antioxidative enzymes in seedlings of Nelumbo nucifera germinated under water.

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Review 5.  Vitamin E: non-antioxidant roles.

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Journal:  Prog Lipid Res       Date:  2000-05       Impact factor: 16.195

6.  Abscisic acid and hypoxic induction of anoxia tolerance in roots of lettuce seedlings.

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Journal:  J Exp Bot       Date:  2000-11       Impact factor: 6.992

7.  Superoxide Dismutase as an Anaerobic Polypeptide : A Key Factor in Recovery from Oxygen Deprivation in Iris pseudacorus?

Authors:  L S Monk; K V Fagerstedt; R M Crawford
Journal:  Plant Physiol       Date:  1987-12       Impact factor: 8.340

8.  Impact of post-anoxia stress on membrane lipids of anoxia-pretreated potato cells. A re-appraisal.

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Journal:  Plant Physiol       Date:  2000-11       Impact factor: 8.340

9.  Ascorbate biosynthesis in Arabidopsis cell suspension culture.

Authors:  M W Davey; C Gilot; G Persiau; J Ostergaard; Y Han; G C Bauw; M C Van Montagu
Journal:  Plant Physiol       Date:  1999-10       Impact factor: 8.340

10.  THE WATER-WATER CYCLE IN CHLOROPLASTS: Scavenging of Active Oxygens and Dissipation of Excess Photons.

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Journal:  Annu Rev Plant Physiol Plant Mol Biol       Date:  1999-06
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  498 in total

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Journal:  Br J Pharmacol       Date:  2003-10       Impact factor: 8.739

2.  Proteomic analysis of molecular response to oxidative stress by the green alga Haematococcus pluvialis (Chlorophyceae).

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Journal:  Planta       Date:  2004-07-17       Impact factor: 4.116

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4.  Difference in chilling-induced flavonoid profiles, antioxidant activity and chilling tolerance between soybean near-isogenic lines for the pubescence color gene.

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Journal:  J Plant Res       Date:  2010-04-29       Impact factor: 2.629

5.  Stability assessment of injectable castor oil-based nano-sized emulsion containing cationic droplets stabilized by poloxamer-chitosan emulsifier films.

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6.  Involvement of sugars in the antioxidant defense against paraquat-induced oxidative stress in potato transformed with yeast invertase gene.

Authors:  M S Sinkevich; N V Naraykina; T I Trunova
Journal:  Dokl Biol Sci       Date:  2010-10-21

7.  Inoculation of Brevibacterium linens RS16 in Oryza sativa genotypes enhanced salinity resistance: Impacts on photosynthetic traits and foliar volatile emissions.

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8.  Increased senescence-associated gene expression and lipid peroxidation induced by iron deficiency in rice roots.

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Journal:  Plant Cell Rep       Date:  2007-08-24       Impact factor: 4.570

9.  Oxygen glucose deprivation (OGD)/re-oxygenation-induced in vitro neuronal cell death involves mitochondrial cyclophilin-D/P53 signaling axis.

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Journal:  Neurochem Res       Date:  2013-01-16       Impact factor: 3.996

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