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Published on: February 2, 2021
Animal models of pediatric chronic kidney disease. Is adenine intake an appropriate model?
Débora Claramunt1, Helena Gil-Peña2, Rocío Fuente1
1University of Oviedo, Spain.
Insights
Pediatric chronic kidney disease (CKD) causes growth impairment. This study evaluates rat models, including 5/6 nephrectomy and adenine diet, to understand CKD-related growth retardation in children.
Area of Science:
- Pediatric Nephrology
- Growth Biology
- Animal Models in Research
Background:
- Pediatric chronic kidney disease (CKD) is characterized by significant growth impairment.
- Growth retardation impacts children's self-esteem and social integration.
- CKD-related factors interfere with growth plate physiology, necessitating animal models for study.
Purpose of the Study:
- To examine the characteristics of the 5/6 nephrectomy rat model for pediatric CKD growth retardation.
- To analyze the high adenine diet-induced CKD model as an alternative research protocol.
- To investigate mechanisms of growth plate dysfunction in pediatric CKD.
Main Methods:
- Utilizing young rats as a model system.
- Inducing chronic kidney disease via 5/6 nephrectomy.
- Inducing chronic kidney disease via high adenine diet.
Main Results:
- The 5/6 nephrectomy model is widely used to study CKD-induced growth retardation.
- The high adenine diet offers an alternative protocol for inducing CKD in research settings.
- Both models allow investigation into the interference with growth plate physiology.
Conclusions:
- Animal models are crucial for studying growth plate dysfunction in pediatric CKD.
- The 5/6 nephrectomy and adenine diet models provide valuable insights into growth impairment.
- Further research using these models can elucidate therapeutic strategies for pediatric CKD growth issues.
Abstract:
Pediatric chronic kidney disease (CKD) has peculiar features. In particular, growth impairment is a major clinical manifestation of CKD that debuts in pediatric age because it presents in a large proportion of infants and children with CKD and has a profound impact on the self-esteem and social integration of the stunted patients. Several factors associated with CKD may lead to growth retardation by interfering with the normal physiology of growth plate, the organ where longitudinal growth rate takes place. The study of growth plate is hardly possible in humans and justifies the use of animal models. Young rats made uremic by 5/6 nephrectomy have been widely used as a model to investigate growth retardation in CKD. This article examines the characteristics of this model and analyzes the utilization of CKD induced by high adenine diet as an alternative research protocol.
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