TY - JOUR
T1 - The redox status of experimental hemorrhagic shock as measured by cyclic voltammetry
AU - Mittal, Anubhav
AU - Göke, Friederike
AU - Flint, Richard
AU - Loveday, Benjamin P T
AU - Thompson, Nichola
AU - Delahunt, Brett
AU - Kilmartin, Paul A.
AU - Cooper, Garth J.S.
AU - MacDonald, Julia
AU - Hickey, Anthony R.J.
AU - Windsor, John A.
AU - Phillips, Anthony R. J.
PY - 2010/5
Y1 - 2010/5
N2 - Hemorrhagic shock (HS) leads to reactive oxygen species production. However, clinicians do not have access to bedside measurements of the redox status during HS. Cyclic voltammetry (CyV) is a simple electrochemical method of measuring redox status. The aims of this study were to 1) report the first application of cyclic voltammetry to measure the acute changes in serum redox status after HS, 2) to contrast it with another severe systemic disease with a different redox pathology (acute pancreatitis [AP]), and 3) to describe the response of CyV over time in a resolving model of AP. In the acute study, 24 male Wistar rats were randomized into three groups: groups 1 (control), 2 (AP), and 3 (HS). In the time-course study, 28 rats were randomized to a sham-control as well as 6 and 24 h post-AP cohorts, respectively. Cyclic voltammetry was performed using a three-electrode system. In the acute study, the first and second voltammetric peaks increased significantly in HS. In contrast, within the AP group, only the first voltammetric peak showed a significant increase. The first voltammetric peak correlated with plasma protein carbonyls (PCs) and with thiobarbituric acid-reactive substances, whereas the second voltammetric peak correlated positively with plasma protein carbonyls. In the second study, the first voltammetric peak correlated with physiological improvements. Here, we showed that serum CyV could respond to the serum redox change in HS and AP. Cyclic voltammetry warrants evaluation as a potential real-time beside measure of a patient's redox status during shock. Copyright © 2010 by the Shock Society.
AB - Hemorrhagic shock (HS) leads to reactive oxygen species production. However, clinicians do not have access to bedside measurements of the redox status during HS. Cyclic voltammetry (CyV) is a simple electrochemical method of measuring redox status. The aims of this study were to 1) report the first application of cyclic voltammetry to measure the acute changes in serum redox status after HS, 2) to contrast it with another severe systemic disease with a different redox pathology (acute pancreatitis [AP]), and 3) to describe the response of CyV over time in a resolving model of AP. In the acute study, 24 male Wistar rats were randomized into three groups: groups 1 (control), 2 (AP), and 3 (HS). In the time-course study, 28 rats were randomized to a sham-control as well as 6 and 24 h post-AP cohorts, respectively. Cyclic voltammetry was performed using a three-electrode system. In the acute study, the first and second voltammetric peaks increased significantly in HS. In contrast, within the AP group, only the first voltammetric peak showed a significant increase. The first voltammetric peak correlated with plasma protein carbonyls (PCs) and with thiobarbituric acid-reactive substances, whereas the second voltammetric peak correlated positively with plasma protein carbonyls. In the second study, the first voltammetric peak correlated with physiological improvements. Here, we showed that serum CyV could respond to the serum redox change in HS and AP. Cyclic voltammetry warrants evaluation as a potential real-time beside measure of a patient's redox status during shock. Copyright © 2010 by the Shock Society.
KW - Acute pancreatitis
KW - Antioxidant
KW - Cyclic voltammetry
KW - Rat
KW - Total antioxidant capacity
KW - Uric acid
U2 - 10.1097/SHK.0b013e3181c0ea12
DO - 10.1097/SHK.0b013e3181c0ea12
M3 - Article
C2 - 19789466
SN - 1073-2322
VL - 33
SP - 460
EP - 466
JO - Shock
JF - Shock
IS - 5
ER -