2006
DOI: 10.1016/j.biopha.2006.07.015
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An in vitro study on the free radical scavenging capacity of ergothioneine: comparison with reduced glutathione, uric acid and trolox

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Cited by 141 publications
(92 citation statements)
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“…Indeed, the chemical reactivity of oxyradicals such as superoxide, hydroxyl and peroxyls radicals towards biological targets is different; accordingly, the relative efficiency of an antioxidant can vary depending on the oxidant [37]. For instance, it has been demonstrated that ergothioneine, a low-molecular-mass thiol, was a protective against oxidation in tissues, scavenging singlet oxygen and hydroxyl radicals [38]. By contrast, this compound did not react with superoxide or hydrogen peroxide and it did not inhibit microsomal lipid peroxidation in the presence of iron [39].…”
Section: Discussionmentioning
confidence: 99%
“…Indeed, the chemical reactivity of oxyradicals such as superoxide, hydroxyl and peroxyls radicals towards biological targets is different; accordingly, the relative efficiency of an antioxidant can vary depending on the oxidant [37]. For instance, it has been demonstrated that ergothioneine, a low-molecular-mass thiol, was a protective against oxidation in tissues, scavenging singlet oxygen and hydroxyl radicals [38]. By contrast, this compound did not react with superoxide or hydrogen peroxide and it did not inhibit microsomal lipid peroxidation in the presence of iron [39].…”
Section: Discussionmentioning
confidence: 99%
“…Similarly, various effects of the addition of EGT either to cells or in vitro in the presence of peroxides have been reported. Franzoni et al (2006) concluded that EGT was the most active scavenger against three species of free radicals Fig. 9.…”
Section: Ergothioneine Is An Antioxidant Against Peroxide In Conidia mentioning
confidence: 99%
“…EGT also has peroxynitrite (ONOO À and ÁONOOH) scavenging capacity, and inhibited oxidation by ONOO À of both purified calf thymus DNA and of DNA in a neuronal hybridoma cell line (Aruoma et al, 1999). EGT provided better protection than GSH against oxidation of a-keto-c-methiolbutyric acid by ONOOH and peroxyl radical (ROOÁ) (Franzoni et al, 2006). EGT also significantly blocked the inhibitory effects of singlet oxygen ( 1 O 2 ) generation by the photosensitive dyes Rose Bengal and phenosafranin .…”
Section: Introductionmentioning
confidence: 95%
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“…Consequently, ERT shows a peculiar stability and reactivity compared to other naturally occurring thiols because it does not auto-oxidize, forms disulfides with difficulty because the standard redox potential at pH 7 of the thiol-disulfide couple of ergothioneine is -0.06 V compared to -0.20 to -0.32 V for other natural thiols, requires a more severe oxidative stress to oxidize, and does not promote the classical Fenton reaction (Figure 15.4). 63 It also has chelating properties toward divalent metallic cations due to its α-amino acid moiety, activates antioxidant enzymes such as glutathione peroxidase and superoxide dismutase (SOD), inhibits superoxide-generating enzymes such as NADPH-cytochrome c reductase, and affects the oxidation of various hemoproteins such as hemoglobin and myoglobin.…”
Section: Ergothioneinementioning
confidence: 99%