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New insights into antioxidant strategies against paraquat toxicity.

Free radical research
June 1, 2014
T Blanco-Ayala et al. (3 authors)
Journal ArticleResearch Support, Non-U.S. Gov'tReviewMolecular Study
Extracted Claims (13)
InterventionDirectionEndpointPopulationDosageImpactClaim #
Paraquat (PQ)
decrease
redox state of the cell
organisms
imbalance
exerts its toxic effects
#1
Paraquat (PQ)
increase
oxidative damage
cell
-
causing
#2
Paraquat (PQ)
increase
cell death
-
-
causing
#3
Paraquat (PQ)
increase
reactive oxygen species
mitochondria
-
increased production
#4
Paraquat (PQ)
decrease
oxygen consumption
-
-
reduction
#5
Paraquat (PQ)
decrease
activity of some respiratory complexes
-
-
reduction
#6
antioxidant therapy
neutral
viable alternative
PQ poisoning
-
suggest
#7
antioxidants naringin, sylimarin, edaravone, Bathysa cuspidata extracts, alpha-lipoic acid, pirfenidone, lysine acetylsalicylate, selenium, quercetin, C-phycocyanin, bacosides, and vitamin C
neutral
treatment against PQ toxicity
-
-
may be useful
#8
these antioxidants
decrease
oxidative stress
-
-
reduction
#9
these antioxidants
decrease
inflammation
-
-
reduction
#10
these antioxidants
increase
antioxidant defenses
-
-
induction
#11
some of the above-mentioned antioxidants
increase
nuclear factor erythroid like-2 (Nrf2)
-
-
induction
#12
induction of nuclear factor erythroid like-2 (Nrf2)
neutral
protective effect against PQ-induced toxicity
-
-
has been involved
#13
Abstract

Paraquat (PQ, 1,1'-dimethyl-4-4'-bipyridinium dichloride) is a highly toxic quaternary ammonium herbicide widely used in agriculture, it exerts its toxic effects mainly because of its redox cycle through the production of superoxide anions in organisms, leading to an imbalance in the redox state of the cell causing oxidative damage and finally cell death. The contribution of mitochondrial dysfunction including increased production of reactive oxygen species besides the reduction in oxygen consumption as well as in the activity of some respiratory complexes has emerged as a key component in the mechanisms through which PQ induces cell death. Although several aspects of PQ-mitochondria interaction remain to be clarified, recent advances have been conducted with reproducible results. Currently, there is no treatment for PQ poisoning; however, several studies taking into account oxidative stress as the main mechanism of PQ-induced toxicity suggest an antioxidant therapy as a viable alternative. In fact, it has been shown that the antioxidants naringin, sylimarin, edaravone, Bathysa cuspidata extracts, alpha-lipoic acid, pirfenidone, lysine acetylsalicylate, selenium, quercetin, C-phycocyanin, bacosides, and vitamin C may be useful in the treatment against PQ toxicity. The main mechanisms involved in the protective effect of these antioxidants include the reduction of oxidative stress and inflammation and the induction of antioxidant defenses. Interestingly, recent findings suggest that the induction of nuclear factor erythroid like-2 (Nrf2), a major regulator of the antioxidant response, by some of the above-mentioned antioxidants, has been involved in the protective effect against PQ-induced toxicity.

Medical Subject Headings (MeSH)
AnimalsAntioxidantsElectron TransportHerbicidesHumansInflammationMitochondriaMitochondrial DiseasesNF-E2-Related Factor 2Neurodegenerative DiseasesOxidative StressParaquatRatsReactive Oxygen Species
Study Links
Citation Metrics
Total Citations172
Citations/Year15.6
Relative Citation Ratio6.89
NIH Percentile95.9%
Research Impact Scores
APT Score0.25
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