Heat shock protein 70-1 gene expression in pediatric heart surgery using blood cardioplegia
Background: In response to many stress stimuli, cardiomyocytes produce a common set of heat shock proteins (HSP). Up-regulation of HSP70-1 (the inducible isoform) is known to reduce the risk of myocardial cell damage during open-heart surgery and seems to be protective against ischemia. We assessed...
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Published in | Clinical chemistry and laboratory medicine Vol. 45; no. 2; pp. 244 - 248 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin
Walter de Gruyter
01.02.2007
New York, NY |
Subjects | |
Online Access | Get full text |
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Summary: | Background: In response to many stress stimuli, cardiomyocytes produce a common set of heat shock proteins (HSP). Up-regulation of HSP70-1 (the inducible isoform) is known to reduce the risk of myocardial cell damage during open-heart surgery and seems to be protective against ischemia. We assessed hsp70-1 gene expression during blood cardioplegic arrest in children undergoing surgical correction of congenital heart defects. Methods: In tissue samples taken from the right atrium of 59 pediatric patients, we examined hsp70-1 gene expression using a real-time quantitative reverse transcription PCR, with 18S rRNA as internal standard. Results: On average, hsp70-1 gene expression was higher than the baseline level by a factor of 1.44± 0.17 (mean±SEM). A significant relationship between hsp70-1 mRNA levels and aortic cross-clamp time was observed (R2=0.069, p=0.044). Conversely, no significant correlation was observed between hsp70-1 mRNA levels and temperature. Conclusions: These data suggest that blood cardioplegia can induce an increment in the expression of hsp70-1, confirming its protective role in ischemia/reperfusion injury. Clin Chem Lab Med 2007;45:244–8. |
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Bibliography: | cclm.2007.030.pdf ark:/67375/QT4-TTZ12JRQ-G istex:CA0BCA27C781ED9BD70A4BE47CDF85404647D11F ArticleID:cclm.45.2.244 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1434-6621 1437-4331 |
DOI: | 10.1515/CCLM.2007.030 |