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Pattern of activin A and follistatin release in a sheep model of cardiopulmonary bypass.

Authors :
Bedford P.
Smith J.A.
Hedger M.P.
McMillan J.
Goldstein J.
Wu H.
Chen Y.
Phillips D.J.
Bedford P.
Smith J.A.
Hedger M.P.
McMillan J.
Goldstein J.
Wu H.
Chen Y.
Phillips D.J.
Publication Year :
2012

Abstract

Objective: Activin A, a member of transforming growth factor-beta superfamily, has been established as a critical cytokine released early in endotoxemia and other inflammatory syndromes. The release of activin A and its binding protein, follistatin during cardiopulmonary bypass (CPB) has not been previously reported. Our study aimed to define the pattern of activin A and follistatin release in a sheep CPB model. Method(s): Control group consisted of left thoractomy alone (n = 6). CPB was performed using either unfractionated heparin (n = 6) or lepirudin (n = 6) as anticoagulant. Unlike heparin, lepirudin does not cause activin A and follistatin release on its own. Serum samples were assayed for activin A, follistatin, tumour necrosis factor-alpha and interleukin-6. Result(s): Compared with the control group, CPB using lepirudin was associated with a biphasic release of activin A. The first peak occurred within the first hour of CPB and a second peak occurred within the early post-operative period, coincident with a large release of follistatin. Close correlation was found between follistatin and IL-6 in the control and lepirudin groups, indicative of a role for follistatin in the acute phase response. In contrast to the control and lepirudin groups, CPB using heparin resulted in a concurrent release of activin A and follistatin. Conclusion(s): CPB is a trigger for the release of biologically-active free activin A into the circulation, at levels considerably greater than that induced by surgery alone. Triggering release of this critical inflammatory cytokine suggests that activin A may contribute to the adverse outcomes associated with systemic inflammation in cardiac surgery. © 2011.

Details

Database :
OAIster
Publication Type :
Electronic Resource
Accession number :
edsoai.on1305128957
Document Type :
Electronic Resource