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Lipid peroxidation, osmotic fragility and antioxidant status in children with acute post-streptococcal

T Devasena1, S Lalitha, K Padma

  • 1Department of Biochemistry, Center for Micronutrient Research, Faculty of Science, Annamalai University, Annamalai Nagar 608 002, Tamil Nadu, India. tedeyes@rediffmail.com

Insights

Children with acute post-streptococcal glomerulonephritis exhibit increased lipid peroxidation and erythrocyte fragility. Their antioxidant enzyme activities and levels of key antioxidants like glutathione are significantly reduced, confirming red blood cell susceptibility to oxidative damage.

Area of Science:

  • Biochemistry
  • Pediatric Nephrology
  • Oxidative Stress Research

Background:

  • Acute post-streptococcal glomerulonephritis (APSGN) is an inflammatory kidney disease.
  • Oxidative stress plays a role in various inflammatory conditions, including APSGN.

Purpose of the Study:

  • To investigate lipid peroxidation (LPO) and antioxidant status in children with APSGN.
  • To assess erythrocyte osmotic fragility in APSGN patients.

Main Methods:

  • Quantified LPO using thiobarbituric acid-reactive substances (TBARS) in plasma and erythrocytes.
  • Measured erythrocyte osmotic fragility.
  • Assessed activities of antioxidant enzymes: superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), and glutathione S-transferase (GST).
  • Measured plasma and erythrocyte levels of ascorbic acid, reduced glutathione (GSH), and total sulphydryl content (TSH).

Main Results:

  • Significantly elevated LPO in plasma and erythrocytes of APSGN children compared to controls.
  • Increased erythrocyte osmotic fragility in APSGN patients.
  • Significantly decreased activities of SOD, CAT, GPx, and GST in APSGN erythrocytes.
  • Significantly depleted plasma and erythrocyte ascorbic acid, GSH, and TSH in APSGN children.

Conclusions:

  • Children with APSGN experience heightened oxidative stress, evidenced by increased LPO and reduced antioxidant defenses.
  • APSGN erythrocytes are more susceptible to oxidative damage and exhibit altered fragility.
  • Findings highlight the role of oxidative stress in the pathophysiology of APSGN in children.

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