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Published on: September 29, 2014
[Selenium concentration in blood and Duchenne-type progressive muscular dystrophy]
1Department of Hygiene, Miyazaki Medical College.
Nihon Rinsho. Japanese Journal of Clinical Medicine
|January 1, 1996
Summary
Selenium (Se) levels and glutathione peroxidase (GSH-Px) activity differ between healthy men and Duchenne muscular dystrophy (DMD) patients. DMD patients show altered Se metabolism and lower GSH-Px activity, particularly concerning selenite release from erythrocytes.
Area of Science:
- Biochemistry
- Clinical Nutrition
- Human Physiology
Context:
- Investigating the role of selenium (Se) and its associated enzyme, glutathione peroxidase (GSH-Px), in human health.
- Understanding age-related changes in Se and GSH-Px in healthy individuals.
- Examining potential alterations in Se and GSH-Px metabolism in Duchenne-type progressive muscular dystrophy (DMD).
Purpose:
- To quantify and compare Se concentrations and GSH-Px activity in plasma and erythrocytes of healthy men and DMD patients.
- To analyze the relationship between aging, Se levels, and GSH-Px activity in both groups.
- To investigate the in vitro kinetics of selenite uptake and release by erythrocytes, with a focus on DMD patients.
Summary:
- In healthy men, erythrocyte Se concentration and GSH-Px activity increase with age, showing a parallel but moderate correlation.
- DMD patients exhibit decreased Se concentrations in both plasma and erythrocytes with age, alongside lower GSH-Px activity (approximately 80% of healthy controls).
- In vitro studies reveal rapid erythrocyte uptake of selenite, followed by plasma release and slow reuptake, with notable differences observed in DMD patients.
Impact:
- Highlights significant differences in selenium metabolism and antioxidant enzyme activity between healthy aging and Duchenne muscular dystrophy.
- Suggests potential implications for selenium supplementation or therapeutic strategies in managing DMD.
- Provides insights into the complex dynamics of selenite transport and utilization within erythrocytes, particularly in the context of muscular dystrophy.
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