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Erythrocyte caspase-3 levels in children with chronic kidney disease
D Polak-Jonkisz1, L Purzyc, M Szcepańska
1Department of Paediatric Nephrology, Wroclaw Medical University, ul. Borowska 213, 50-556 Wroclaw, Poland. dorota.polak-jonkisz@am.wroc.pl
Insights
Red blood cell (RBC) aging in children with chronic kidney disease (CKD) increases with disease progression. Caspase-3 activity rises, while lactate dehydrogenase (LDH) and ATP levels decline in late-stage CKD, indicating energy imbalance.
Area of Science:
- Biochemistry
- Hematology
- Nephrology
Background:
- Chronic kidney disease (CKD) alters red blood cell (RBC) structure and metabolism.
- Factors like uremic toxins induce premature RBC aging and apoptosis in CKD patients.
- Understanding cellular responses in CKD is crucial for managing disease progression.
Purpose of the Study:
- To evaluate caspase-3 activity, lactate dehydrogenase (LDH) levels, and adenosine triphosphate (ATP) concentrations in erythrocytes of children with CKD.
- To correlate these erythrocyte parameters with the progression of chronic kidney disease.
Main Methods:
- Spectrophotometric assays were used to measure caspase-3 and LDH activity in hemolyzed erythrocytes.
- Adenosine triphosphate (ATP) concentrations were determined using a luciferin-luciferase kit.
- Sixty CKD children (Stages I-IV) and 25 healthy children were included.
Main Results:
- Lactate dehydrogenase (LDH) and ATP levels gradually increased from CKD Stage I to III, but decreased significantly in Stage IV compared to controls.
- Caspase-3 activity was comparable to healthy children in Stage I and peaked in Stage III.
- Stage IV CKD showed significantly lower LDH and ATP levels than the control group.
Conclusions:
- Caspase-3 activity in RBCs of children with CKD increases as the disease progresses.
- Decreased LDH activity and ATP concentration in Stage IV CKD suggest a compromised cellular energy balance.
- These findings highlight significant alterations in RBC metabolism and integrity during CKD progression.
Objectives:
In chronic kidney disease (CKD), a number of intra- and extracellular factors, e.g., uremic toxins, mechanic, oxidative or osmotic stress - induce changes (rearrangements) in the structure of cytoplasmatic membrane, while also simultaneously deregulating blood cell metabolism and, in consequence, contributing to preliminary ageing and suicidal death of red blood cells (RBCs).The aim of the reported study was an evaluation of caspase-3 and lactate dehydrogenase activities and of ATP concentrations in erythrocytes as cellular responses to CKD progress.
Design And Methods:
Conservatively treated sixty (60) CKD children were enrolled into the study and divided, according to CKD progression (stage I-IV). The control group consisted of twenty-five (25) healthy children. The activity of caspase-3 (Casp-3) and lactate dehydrogenase (LDH) were spectrophotometrically assayed in haemolysed erythrocytes. Adenosine triphosphate (ATP(e)) concentrations were measured by means of a luciferin-luciferase kit.
Results:
A gradual increase of LDH and ATP levels was observed in transition from CKD stage I to stage III. In Group IV, the levels of those parameters were statistically significantly lower than in the control group. The activity of Casp-3 in Group I was comparable to that in healthy children. The highest activity of Casp-3 was observed in Group III.
Conclusions:
1. The activity of caspase-3 in RBCs of CKD children grows with progression of the disease. 2. The lower LDH activities and the ATP concentration drop below the values characteristic for the control group, as observed in stage IV of CKD, indicate a compromised energy balance.
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