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Does oxidative stress play a role in altered plasma protein homeostasis in pregnancy-induced hypertension?
S Asmathulla1, Bidhan Chandra Koner, D Papa
1Department of Biochemistry, Jawaharlal Institute of Postgraduate Medical Education & Research Institute, Puducherry, India.
Insights
Oxidative stress in pregnancy-induced hypertension (PIH) damages plasma proteins, leading to lower levels. Hypersialylation may protect proteins from this oxidative damage.
Area of Science:
- Biochemistry
- Obstetrics
- Pathophysiology
Background:
- Pregnancy-induced hypertension (PIH) is linked to oxidative stress and reduced plasma proteins.
- This study investigates the impact of oxidative stress on plasma protein levels in PIH.
Purpose of the Study:
- To examine the relationship between oxidative stress markers and plasma protein levels in various forms of PIH.
- To understand the role of protein damage in the pathogenesis of PIH.
Main Methods:
- Quantified serum total proteins, albumin, globulin, malondialdehyde, protein carbonyls (PC), and protein bound sialic acid (PBSA) in PIH subgroups and healthy controls.
- Utilized electrophoresis to assess protein damage.
Main Results:
- PIH subgroups showed significantly increased malondialdehyde, PC, and PBSA, with decreased total proteins and albumin compared to healthy controls.
- Globulin levels decreased only in eclampsia.
- Negative correlation observed between malondialdehyde/PC and albumin; electrophoretogram indicated protein fragmentation and aggregation in eclampsia.
Conclusions:
- Oxidative protein damage contributes to reduced serum protein levels in PIH.
- Hypersialylation of plasma proteins is a potential protective response against oxidative damage in PIH.
Background:
Pregnancy-induced hypertension (PIH) is associated with oxidative stress and low plasma proteins. This study explored the effect of oxidative stress on plasma protein level in PIH.
Methods:
Serum total proteins (TP), albumin, globulin, malondialdehyde, protein carbonyls (PC) and protein bound sialic acid (PBSA) were measured in gestational hypertensive, pre-eclamptic, eclamptic and healthy pregnant women (n=20/group). Serum proteins were separated by electrophoresis for assessing protein damage.
Results:
Serum TP and albumin decreased and malondialdehyde, PC & PBSA increased significantly in all PIH subgroups as compared to healthy pregnant subjects. Serum globulin levels decreased only in eclampsia. Malondialdehyde and PC negatively correlated with albumin level. Protein fragmentation and aggregation in eclampsia were evident from electrophoretogram.
Conclusion:
We conclude that oxidative damages to proteins contribute to decreased serum protein levels in PIH and hypersialylation of plasma proteins is probably body’s protective mechanism to combat oxidative protein damage in PIH.
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