Details

Autor(en) / Beteiligte

• Manevich, Y.
• Hutchens, S.
• Halushka, P.V.
• Tew, K.D.
• Townsend, D.M.
• Jauch, E.C.
• Borg, K.

Titel

Peroxiredoxin VI oxidation in cerebrospinal fluid correlates with traumatic brain injury outcome

Ist Teil von

• Free radical biology & medicine, 2014-07, Vol.72, p.210-221

Ort / Verlag

United States: Elsevier Inc

Erscheinungsjahr

2014

Quelle

MEDLINE

Beschreibungen/Notizen

• Traumatic brain injury (TBI) patients would benefit from the identification of reliable biomarkers to predict outcomes and treatment strategies. In our study, cerebrospinal fluid (CSF) from patients with severe TBI was evaluated for oxidant stress-mediated damage progression after hospital admission and subsequent ventriculostomy placement. Interestingly, substantial levels of peroxiredoxin VI (Prdx6), a major antioxidant enzyme normally found in astrocytes, were detected in CSF from control and TBI patients and were not associated with blood contamination. Functionally, Prdx6 and its associated binding partner glutathione S-transferase Pi (GSTP1-1, also detected in CSF) act in tandem to detoxify lipid peroxidation damage to membranes. We found Prdx6 was fully active in CSF of control patients but becomes significantly inactivated (oxidized) in TBI. Furthermore, significant and progressive oxidation of “buried” protein thiols in CSF of TBI patients (compared to those of nontrauma controls) was detected over a 24-h period after hospital admission, with increased oxidation correlating with severity of trauma. Conversely, recovery of Prdx6 activity after 24h indicated more favorable patient outcome. Not only is this the first report of an extracellular form of Prdx6 but also the first report of its detection at a substantial level in CSF. Taken together, our data suggest a meaningful correlation between TBI-initiated oxidation of Prdx6, its specific phospholipid hydroperoxide peroxidase activity, and severity of trauma outcome. Consequently, we propose that Prdx6 redox status detection has the potential to be a biomarker for TBI outcome and a future indicator of therapeutic efficacy. [Display omitted] •TBI induces fast rise and decay of GSH and oxidation of buried protein thiols in CSF.•Prdx6 was detected in CSF at substantial levels.•TBI results in Prdx6 oxidation and deactivation of its peroxidase function in CSF.•Prdx6 redox state correlates with TBI neurological outcome.•Prdx6 could serve as a biomarker of TBI outcome and of therapeutic efficacy.