Imbalance between free radical propagation and antioxidants status in children with nephrotic syndrome. Benha Medical Journal,14(3):219-225
• 1997
Publication Information
Authors
R Sanad, and AM El Abd
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publication.type
Local
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Abstract
Oxygen-free radical have been implicated in a variety of disease
processes including nephrotic syndrome. In this study we investigated the
free radical activation products and antioxidant status in children with
nephrotic syndrome compared with a control group. Serum lipid
peroxides (LP) and selenium levels and red blood cell glutathione
peroxidase (GSH-PX) and superoxide dismutase (SOD) activities were
measured in 35 children (28 males and 7 females) with nephrotic
syndrome. Similar number of apparently healthy children with
appropriate age and sex were used as a control group. Children with
nephrotic syndrome had significantly higher levels of LP (3.37+0.5
nmol/ml) and lower level of serum selenium (150 ±35 ug/L) and red
blood cell GSH-PX (32.6+7.8 U/gHb) and SOD (1116 ±151 U/gHb)
respectively) when compared with the corresponding levels of the control
group (2.53 ±0.6nmol/ml, 230 ±43 ug/L. 51.8 ±13.8 U/gHb & 1422 ±
277 U/g Hb respectively). We concluded that imbalance between
generation of oxygen free radicals and antioxidant status may have
etiological implications for nephrotic syndrome.
processes including nephrotic syndrome. In this study we investigated the
free radical activation products and antioxidant status in children with
nephrotic syndrome compared with a control group. Serum lipid
peroxides (LP) and selenium levels and red blood cell glutathione
peroxidase (GSH-PX) and superoxide dismutase (SOD) activities were
measured in 35 children (28 males and 7 females) with nephrotic
syndrome. Similar number of apparently healthy children with
appropriate age and sex were used as a control group. Children with
nephrotic syndrome had significantly higher levels of LP (3.37+0.5
nmol/ml) and lower level of serum selenium (150 ±35 ug/L) and red
blood cell GSH-PX (32.6+7.8 U/gHb) and SOD (1116 ±151 U/gHb)
respectively) when compared with the corresponding levels of the control
group (2.53 ±0.6nmol/ml, 230 ±43 ug/L. 51.8 ±13.8 U/gHb & 1422 ±
277 U/g Hb respectively). We concluded that imbalance between
generation of oxygen free radicals and antioxidant status may have
etiological implications for nephrotic syndrome.
Staff Members - Benha University