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Glucocorticoid receptor expression and binding capacity in patients with burn injury
- Source :
- Europe PubMed Central
-
Abstract
- Burn injuries are associated with strong inflammation and risk of secondary sepsis which both may affect the function of the glucocorticoid receptor (GR). The aim of this study was to determine GR expression and binding capacity in leucocytes from patients admitted to a tertiary burn center.Blood was sampled from 13 patients on admission and days 7, 14 and 21, and once from 16 healthy subjects. Patients were grouped according to the extent of burn and to any sepsis on day 7. Expression and binding capacity of GR were determined as arbitrary units using flow cytometry.GR expression and binding capacity were increased compared to healthy subjects in most circulating leucocyte subsets on admission irrespective of burn size. Patients with sepsis on day 7 displayed increased GR expression in T lymphocytes (51.8%, P0.01) compared to admission. There was a negative correlation between GR binding capacity in neutrophils and burn size after 14 days (P0.05).GR expression and binding capacity are increased in most types of circulating leucocytes of severely burned patients on their admission to specialized burn care. If sepsis is present after 1 week, it is associated with higher GR expression in T lymphocytes and NK cells.
- Subjects :
- 0301 basic medicine
Adult
Male
medicine.medical_specialty
Burn injury
Inflammation
Bioinformatics
Sepsis
03 medical and health sciences
Leukocyte Count
0302 clinical medicine
Glucocorticoid receptor
Receptors, Glucocorticoid
Internal medicine
medicine
Leukocytes
Humans
In patient
Receptor
Aged
Aged, 80 and over
biology
business.industry
C-reactive protein
030208 emergency & critical care medicine
General Medicine
Middle Aged
medicine.disease
030104 developmental biology
Anesthesiology and Pain Medicine
Endocrinology
C-Reactive Protein
Apoptosis
biology.protein
Female
medicine.symptom
business
Burns
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- Europe PubMed Central
- Accession number :
- edsair.doi.dedup.....680b0b0ae6a7a8be4e6120da502e0903