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Perfluorocarbon administration during cardiopulmonary bypass in rats: an inflammatory link to adverse outcome?

Publication ,  Journal Article
de Lange, F; Yoshitani, K; Proia, AD; Mackensen, GB; Grocott, HP
Published in: Anesth Analg
January 2008

BACKGROUND: Perfluorocarbon (PFC) emulsions are artificial oxygen carriers that have been shown to attenuate the effects of air embolism. Cerebral air embolism, known to occur during cardiopulmonary bypass (CPB), may contribute to adverse cerebral outcomes after cardiac surgery. We designed this study to evaluate the effect of a 60% PFC emulsion (perfluoro-tert-butylcyclohexane; PTBCH) on the inflammatory response and neurocognitive outcome of rats after CPB. METHODS: Twenty-eight Sprague Dawley rats subjected to 60 min of CPB were randomly divided into two groups: PTBCH CPB animals receiving 3 mL/kg of PTBCH into the venous reservoir and control CPB animals receiving 3 mL/kg of 0.9% saline. At several time points, the cytokines interleukin (IL)-1beta, IL-6, IL-10, and tumor necrosis factor (TNF)-alpha were measured. Neurocognitive testing was planned postoperatively using the Morris water maze. Histologic samples were obtained in a separate series of experiments. RESULTS: Physiologic variables were comparable between groups, but the PTBCH CPB animals required more phenylephrine compared with the controls. Cytokine levels in the PTBCH CPB group were significantly higher than in the control group at 2 and 4 h after CPB (P < 0.05). Neurocognitive outcome could not be evaluated as none of the animals in the PTBCH CPB group survived. Myocardial histological analysis revealed increased areas of contraction band necrosis in the PTBCH CPB animals (P = 0.034). CONCLUSIONS: Administration of PTBCH during CPB was associated with an excessive release of cytokines. This enhanced inflammatory response with subsequent hypotension may have contributed to mortality in rats receiving PTBCH. The observed patterns of myocardial injury indicate global hypoperfusion and catecholamine excess.

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Published In

Anesth Analg

DOI

EISSN

1526-7598

Publication Date

January 2008

Volume

106

Issue

1

Start / End Page

24 / 31

Location

United States

Related Subject Headings

  • Tumor Necrosis Factor-alpha
  • Time Factors
  • Rats, Sprague-Dawley
  • Rats
  • Myocardium
  • Models, Animal
  • Male
  • Lung
  • Kidney
  • Interleukins
 

Citation

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de Lange, F., Yoshitani, K., Proia, A. D., Mackensen, G. B., & Grocott, H. P. (2008). Perfluorocarbon administration during cardiopulmonary bypass in rats: an inflammatory link to adverse outcome? Anesth Analg, 106(1), 24–31. https://doi.org/10.1213/01.ane.0000297439.90773.c7
Lange, Fellery de, Kenji Yoshitani, Alan D. Proia, G Burkhard Mackensen, and Hilary P. Grocott. “Perfluorocarbon administration during cardiopulmonary bypass in rats: an inflammatory link to adverse outcome?Anesth Analg 106, no. 1 (January 2008): 24–31. https://doi.org/10.1213/01.ane.0000297439.90773.c7.
de Lange F, Yoshitani K, Proia AD, Mackensen GB, Grocott HP. Perfluorocarbon administration during cardiopulmonary bypass in rats: an inflammatory link to adverse outcome? Anesth Analg. 2008 Jan;106(1):24–31.
de Lange, Fellery, et al. “Perfluorocarbon administration during cardiopulmonary bypass in rats: an inflammatory link to adverse outcome?Anesth Analg, vol. 106, no. 1, Jan. 2008, pp. 24–31. Pubmed, doi:10.1213/01.ane.0000297439.90773.c7.
de Lange F, Yoshitani K, Proia AD, Mackensen GB, Grocott HP. Perfluorocarbon administration during cardiopulmonary bypass in rats: an inflammatory link to adverse outcome? Anesth Analg. 2008 Jan;106(1):24–31.

Published In

Anesth Analg

DOI

EISSN

1526-7598

Publication Date

January 2008

Volume

106

Issue

1

Start / End Page

24 / 31

Location

United States

Related Subject Headings

  • Tumor Necrosis Factor-alpha
  • Time Factors
  • Rats, Sprague-Dawley
  • Rats
  • Myocardium
  • Models, Animal
  • Male
  • Lung
  • Kidney
  • Interleukins