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Effect of myocardial protection and perfusion temperature on production of cytokines and nitric oxide during cardiopulmonary bypass.

作者信息

Tavares-Murta Beatriz Martins, Cordeiro Adriana Oliveira, Murta Eddie Fernando Candido, Cunha Fernando de Queiroz, Bisinotto Flora Margarida Barra

机构信息

Department of Biological Sciences, UFTM, Minas Gerais, MG, Brazil.

出版信息

Acta Cir Bras. 2007 Jul-Aug;22(4):243-50. doi: 10.1590/s0102-86502007000400003.

DOI:10.1590/s0102-86502007000400003
PMID:17625660
Abstract

PURPOSE

To investigate the effects of different conditions used during cardiopulmonary bypass (CPB) surgery on accompanying production of cytokine and nitric oxide (NO).

METHODS

Patients undergoing CPB for the first time were prospectively enrolled and divided into two groups according to CPB parameters performed: i) normothermia (36.5-37 degrees C) with blood cardioplegia (NB group, n=10) and ii) hypothermia (29-31 degrees C) with crystalloid cardioplegia (HC group, n=10). Plasma samples obtained following intubation (baseline), during (5 and 30 min) and after (4 and 24 h) CPB were assayed for cytokines (ELISA) and NO metabolites (Griess reaction).

RESULTS

Peak concentrations of interleukin (IL)-6 and IL-8 were reached at 4 h post CPB in both groups, but in the HC group those levels increased earlier and persisted for longer (24 h) compared to baseline (P < 0.05). IL-10 levels also increased at 4 h compared to baseline, but only significantly so in the HC group. NO metabolites were reduced in HC group at all time points compared to baseline (P < 0.05), while no significant differences were detected in the NB group.

CONCLUSION

The association between increased systemic levels of cytokines and reduced NO production in the HC group suggests that different myocardial protection and/or perfusion temperature used during CPB may contribute to the extent of inflammatory response.

摘要

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