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Relationship: 948
Title
Peptide Oxidation leads to Oxidation, Glutathione
Upstream event
Downstream event
AOPs Referencing Relationship
Taxonomic Applicability
Sex Applicability
| Sex | Evidence |
|---|---|
| Unspecific | High |
Life Stage Applicability
| Term | Evidence |
|---|---|
| All life stages | High |
Under physiological conditions, glutathione (GSH) functions as an anti-oxidant by defending the cell from oxidative stress (Kalinina et al., 2014). It is predominantly found in the reduced form while the oxidized form glutathione disulfide (GSSG) generally does not exceed 1% of its total cellular content. Exposure to oxidants like peroxides leads to the oxidation of intracellular GSH, resulting in the formation of GSSG which alters the redox state of the cell (Pullar et al., 2001). This imbalance in the GSH/GSSG ratio is a marker of oxidative stress.
| ID | Experimental Design | Species | Upstream Observation | Downstream Observation | Citation (first author, year) | Notes |
|---|
| Title | First Author | Biological Plausibility |
Dose Concordance |
Temporal Concordance |
Incidence Concordance |
|---|
Biological Plausibility
Dose Concordance Evidence
Temporal Concordance Evidence
Incidence Concordance Evidence
Uncertainties and Inconsistencies
One study reported that only a small amount of GSH was oxidized to GSSG in a concentration-dependent manner when HUVECs were exposed to hypochlorous acid (HOCl) while the remaining GSH was converted to another product glutathione sulfonamide. This discrepancy may be due to the different oxidant used in this study (Pullar et al., 2001).
Is it known how much change in the first event is needed to impact the second? Are there known modulators of the response-response relationships? Are there models or extrapolation approaches that help describe those relationships?
From the studies mentioned above, it appears that any oxidant (e.g. tBH, H2O2, ultrafine particles) with a minimum concentration of 10 μM would be sufficient to induce oxidation of GSH and cause an increase in GSSG levels. However, treatment with a concentration of25 nM of HOCl was shown to oxidize GSH, but did not produce GSSG (Pullar et al., 2001).
Response-response Relationship
Time-scale
Known Feedforward/Feedback loops influencing this KER
There are many studies showing oxidation of GSH following oxidant exposure in human endothelial cells, particularly umbilical and aortic endothelial cells (Dhar et al., 2010; Du et al., 2013; Montecinos et al., 2007; Park, 2013; Schuppe et al., 1992; van Gorp et al., 1999, 2002), while two studies in rat and bovine aortic endothelial cells support this relationship (Dhar et al., 2010; De Pascali et al., 2014).