Skip to main content
. 2018 Feb 28;8(5):417–425. doi: 10.3892/br.2018.1071

Table III.

Effect of CM administration on renal functions parameters and oxidative stress markers in the study population.

A, CAD group (early CIN patients excluded)

Sampling time Creatinine (mg/dl) Urea (mg/dl) GSH (µmol/g Hb) TAC (mmol DPPH/L plasma) TBARS (µmol/l) Catalase (U/mg Hb) Carbonyls (nmol/mg protein)
t=0 0.806±0.117 39.6±12.4 0.588±0.482 0.905±0.128 3.58±1.31 174±30.1 1.26±0.412
t=1 h 0.828±0.192 38.4±14.8 0.63±0.493 0.956±0.114b 3.46±1.26 179±45.1 0.840±0.228b
t=4–6 h 0.876±0.222 34.1±11.4a 1.45±1.02c 0.926±0.105 4.71±1.94a 163±35.1a 0.889± 0.248a

B, Control group

Sampling time Creatinine (mg/dl) Urea (mg/dl) GSH (µmol/g Hb) TAC (mmol DPPH/L plasma) TBARS (µmol/l) Catalase (U/mg Hb) Carbonyls (nmol/mg protein)

t=0 1.06±0.190 42.8±23.2 1.91± 0.807 0.956± 0.150 7.32± 1.34 192± 67.8 0.793± 0.141
t=1 h 1.04±0.151 49.6±24.0 2.01±0.43 0.945±0.157 7.81±1.88 193±94.1 0.794± 0.128
t=5–10 h 0.839±0.242b 39.8±14.9 2.13±1.14 0.933±0.161 8.06±3.26 223±108 0.785±0.180

Statistical significance compared to t=0

a

P<0.05

b

P<0.01

c

P<0.001. CAD, coronary artery disease; CIN, contrast induced nephropathy; CM, contrast medium; GSH, glutathione; TAC, total anti-oxidant activity; TBARS, thio-barbituric acid reactive species.