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Published on: February 13, 2019
Changes in glutamic oxaloacetic transaminase 2 during rat physiological and pathological cardiomyocyte hypertrophy
Xin Liu1, Xiaolu Li2, Haotan Zhou3
1Department of Pediatric Cardiac Center, Beijing Anzhen Hospital, Capital Medical University, Beijing, 100029, China. 18811563661@163.com.
Insights
Glutamic oxaloacetic transaminase (GOT) levels differ in rat heart muscle growth. GOT2 protein increased in normal growth but decreased in pathological hypertrophy, suggesting a regulatory role in heart disease.
Area of Science:
- Cardiology
- Molecular Biology
- Physiology
Background:
- Physiological and pathological cardiomyocyte hypertrophy are key in congenital heart disease.
- Glutamic oxaloacetic transaminase (GOT) indicates myocardial injury.
- Investigates GOT changes during rat cardiomyocyte hypertrophy.
Purpose of the Study:
- To examine GOT mRNA, activity, and GOT2 protein levels during physiological and pathological cardiomyocyte hypertrophy in rats.
- To understand GOT's role in ventricular hypertrophy associated with congenital heart disease.
Main Methods:
- RNA-sequencing and colorimetric assays for GOT mRNA and activity.
- Western blotting and immunofluorescence for GOT2 protein.
- Histological methods (H&E, WGA) for cardiomyocyte morphology.
Main Results:
- GOT mRNA, activity, and GOT2 protein increased with age-related physiological hypertrophy in juvenile rats.
- GOT2 protein levels decreased in hypoxia-induced pathological hypertrophy.
- Significant differences in GOT2 expression correlate with hypertrophy type.
Conclusions:
- GOT2 may play a regulatory role in both physiological and pathological myocardial hypertrophy in rats.
- Reduced GOT2 levels might contribute to pathological hypertrophy and subsequent heart failure.
- Findings suggest GOT2 as a potential therapeutic target for heart conditions.
Background:
Physiological and pathological cardiomyocyte hypertrophy are important pathophysiological processes of adult congenital heart disease-associated ventricular hypertrophy. Glutamic oxaloacetic transaminase (GOT) is a vital marker of myocardial injury. This study aimed to investigate the changes in GOT levels during physiological and pathological cardiomyocyte hypertrophy in rats.
Methods:
RNA-seq analysis and colorimetric methods were used to evaluate the changes in GOT mRNA and activity, respectively. GOT2 protein expression was detected by western blotting and immunofluorescence. Hematoxylin-eosin and wheat germ agglutinin methods were used to observe changes in rat cardiomyocyte morphology.
Results:
In juvenile rat hearts, GOT mRNA expression and activity, and GOT2 protein level increased with age-related physiological cardiomyocyte hypertrophy; however, GOT2 protein level was reduced in hypoxia-induced pathological cardiomyocyte hypertrophy.
Conclusions:
GOT2 may regulate physiological and pathological myocardial hypertrophy in rats. We speculated that the low GOT2 level contributed to the rapid occurrence of pathological cardiomyocyte hypertrophy, causing strong plasticity of right ventricular cardiomyocytes in the early postnatal period and heart failure in adulthood.
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