2022
DOI: 10.1007/s00726-021-03121-5
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Cytoprotective effect of taurine against sodium chlorate-induced oxidative damage in human red blood cells: an ex vivo study

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Cited by 10 publications
(9 citation statements)
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“…These data demonstrate that GCs strongly promote Tau secretion and spreading in vivo. To assess whether this spreading occurs via type 1 UPS, we initiated a second hTau spreading experiment with epigallocatechin gallate (EGCG), a potent inhibitor of Tau aggregation that attenuates its secretion via type 1 UPS 37,47 and can be used in vivo, unlike other inhibitors of type 1 UPS 48,49 . We rst veri ed the ability of EGCG to reduce GC-induced Tau secretion in brain slices (Fig.…”
Section: Resultsmentioning
confidence: 99%
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“…These data demonstrate that GCs strongly promote Tau secretion and spreading in vivo. To assess whether this spreading occurs via type 1 UPS, we initiated a second hTau spreading experiment with epigallocatechin gallate (EGCG), a potent inhibitor of Tau aggregation that attenuates its secretion via type 1 UPS 37,47 and can be used in vivo, unlike other inhibitors of type 1 UPS 48,49 . We rst veri ed the ability of EGCG to reduce GC-induced Tau secretion in brain slices (Fig.…”
Section: Resultsmentioning
confidence: 99%
“…However, EGCG also alters lipid membrane properties 51,52 and could alter Tau secretion/uptake via this mechanism. Other drugs that block type 1 UPS, such as NaClO 3 and methyl-b-cyclodextrin, have similarly pleiotropic effects (and further cannot be used in vivo due to their blood brain barrier impermeability and toxicity, respectively 48,49 ), making it di cult to de nitively demonstrate that secretion via type 1 UPS is the primary driver of GC-induced Tau propagation in vivo. However, given the relative amount of Tau reported to undergo secretion in vesicle-free form (~ 90%) 22 , we think it is reasonable to assume that type 1 UPS contributes substantially to GC-induced Tau spreading in vivo.…”
Section: Discussionmentioning
confidence: 99%
“…7). On the other hand, several studies have revealed the exciting effects of TAU on erythrocytes [38][39][40][41][42][43]. TAU is not considered a classic radical scavenger or a regulator of cellular antioxidant defense mechanisms [145][146][147].…”
Section: •-mentioning
confidence: 99%
“…Several studies have also mentioned the positive effects of TAU on erythrocytes [38][39][40][41][42][43]. In this regard, TAU significantly suppressed oxidative stress and its associated complications, such as lipid peroxidation and protein carbonylation in erythrocytes exposed to toxic insults [39][40][41][42][43]. TAU also significantly enhanced the level of antioxidant enzymes such as catalase, superoxide dismutase, glutathione-S-transferase, and glutathione peroxidase in erythrocytes [39,40,42,43].…”
Section: Introductionmentioning
confidence: 99%
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