Systemic inflammation and oxidative stress post-lung resection: effect of pretreatment with N-acetylcysteine
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Accepted version
Supporting information
Author(s)
Bastin, AJ
Davies, N
Lim, E
Quinlan, GJ
Griffiths, MJ
Type
Journal Article
Abstract
Background and objective
N-acetylcysteine has been used to treat a variety of lung diseases, where is it thought to have an antioxidant effect. In a randomized placebo-controlled double-blind study, the effect of N-acetylcysteine on systemic inflammation and oxidative damage was examined in patients undergoing lung resection, a human model of acute lung injury.
Methods
Eligible adults were randomized to receive preoperative infusion of N-acetylcysteine (240 mg/kg over 12 h) or placebo. Plasma thiols, interleukin-6, 8-isoprostane, ischaemia-modified albumin, red blood cell glutathione and exhaled breath condensate pH were measured pre- and post-operatively as markers of local and systemic inflammation and oxidative stress.
Results
Patients undergoing lung resection and one-lung ventilation exhibited significant postoperative inflammation and oxidative damage. Postoperative plasma thiol concentration was significantly higher in the N-acetylcysteine-treated group. However, there was no significant difference in any of the measured biomarkers of inflammation or oxidative damage, or in clinical outcomes, between N-acetylcysteine and placebo groups.
Conclusion
Preoperative administration of N-acetylcysteine did not attenuate postoperative systemic or pulmonary inflammation or oxidative damage after lung resection.
N-acetylcysteine has been used to treat a variety of lung diseases, where is it thought to have an antioxidant effect. In a randomized placebo-controlled double-blind study, the effect of N-acetylcysteine on systemic inflammation and oxidative damage was examined in patients undergoing lung resection, a human model of acute lung injury.
Methods
Eligible adults were randomized to receive preoperative infusion of N-acetylcysteine (240 mg/kg over 12 h) or placebo. Plasma thiols, interleukin-6, 8-isoprostane, ischaemia-modified albumin, red blood cell glutathione and exhaled breath condensate pH were measured pre- and post-operatively as markers of local and systemic inflammation and oxidative stress.
Results
Patients undergoing lung resection and one-lung ventilation exhibited significant postoperative inflammation and oxidative damage. Postoperative plasma thiol concentration was significantly higher in the N-acetylcysteine-treated group. However, there was no significant difference in any of the measured biomarkers of inflammation or oxidative damage, or in clinical outcomes, between N-acetylcysteine and placebo groups.
Conclusion
Preoperative administration of N-acetylcysteine did not attenuate postoperative systemic or pulmonary inflammation or oxidative damage after lung resection.
Date Issued
2016-01
Date Acceptance
2015-07-28
Citation
Respirology, 2016, 21 (1), pp.180-187
ISSN
1440-1843
Publisher
Wiley
Start Page
180
End Page
187
Journal / Book Title
Respirology
Volume
21
Issue
1
Copyright Statement
© 2015 Asian Pacific Society of Respirology. This is the accepted version of the following article, which has been published in final form at http://onlinelibrary.wiley.com/doi/10.1111/resp.12662/abstract
Sponsor
Royal College of Physicians
British Lung Foundation
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000367312400026&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Grant Number
Dr A Bastin
TC07/10
Subjects
Science & Technology
Life Sciences & Biomedicine
Respiratory System
critical care medicine
inflammation
lung injury
lung cancer
thoracic surgery
Respiratory-distress-syndrome
Placebo-controlled trail
Double-blind
Pulmonary resection
Antioxidant treatment
Septic shock
Injury
Damage
Ventilation
Surgery
Critical care medicine
Inflammation
Lung cancer
Lung injury
Thoracic surgery
Medical And Health Sciences
Publication Status
Published
Date Publish Online
2015-10-27