the nitrated fatty acid 10-nitro-oleate diminishes severity of lps-induced acute lung injury in mice氮化脂肪酸10-nitro-oleate减少的严重程度lps-induced在小鼠急性肺损伤.pdfVIP

the nitrated fatty acid 10-nitro-oleate diminishes severity of lps-induced acute lung injury in mice氮化脂肪酸10-nitro-oleate减少的严重程度lps-induced在小鼠急性肺损伤.pdf

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the nitrated fatty acid 10-nitro-oleate diminishes severity of lps-induced acute lung injury in mice氮化脂肪酸10-nitro-oleate减少的严重程度lps-induced在小鼠急性肺损伤

Hindawi Publishing Corporation PPAR Research Volume 2012, Article ID 617063, 12 pages doi:10.1155/2012/617063 Research Article The Nitrated Fatty Acid 10-Nitro-oleate Diminishes Severity of LPS-Induced Acute Lung Injury in Mice Aravind T. Reddy, Sowmya P. Lakshmi, and Raju C. Reddy Department of Medicine, Division of Pulmonary, Allergy and Critical Care Medicine, Emory University and Atlanta VA Medical Center, Atlanta, GA 30033, USA Correspondence should be addressed to Raju C. Reddy, raju.reddy@ Received 24 February 2012; Accepted 21 April 2012 Academic Editor: Jesse Roman Copyright © 2012 Aravind T. Reddy et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Acute lung injury (ALI) is an inflammatory condition culminating in respiratory failure. There is currently no effective pharmacological treatment. Nitrated fatty acids (NFAs) have been shown to exert anti-inflammatory effects. We therefore hypothesized that delivery of NFAs directly to the site of inflammation would reduce the severity of ALI. Pulmonary delivery of 10-nitro-oleate following endotoxin-induced ALI in mice reduced markers of lung inflammation and injury, including capillary leakage, lung edema, infiltration of neutrophils into the lung, and oxidant stress, as well as plasma levels of proinflammatory cytokines. Nitro-oleate delivery likewise downregulated expression of proinflammatory genes by alveolar macrophages, key cells in regulation of lung inflammation. These effects may be accounted for by the observed increases in the activity of PPAR-γ and the PPAR-γ-induced antioxidant transcription

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