15 PROTECTIVE EFFECTS OF OXIDIZED PHOSPHOLIPIDS ON VENTILATOR-INDUCED LUNG INJURY. (1st March 2006)
- Record Type:
- Journal Article
- Title:
- 15 PROTECTIVE EFFECTS OF OXIDIZED PHOSPHOLIPIDS ON VENTILATOR-INDUCED LUNG INJURY. (1st March 2006)
- Main Title:
- 15 PROTECTIVE EFFECTS OF OXIDIZED PHOSPHOLIPIDS ON VENTILATOR-INDUCED LUNG INJURY.
- Authors:
- Burdette, D. O.
Nonas, S. A.
Miller, I.
Birukova, A. A.
Chatchavalvanich, S.
Garcia, J. G.N.
Birukov, K. G. - Abstract:
- Abstract : Purpose of Study: Acute lung injury (ALI) is a devastating syndrome characterized by pulmonary inflammation and vascular barrier dysfunction with protein-rich edema. Mechanical ventilation at high tidal volumes can worsen existing ALI and even cause ventilator-induced lung injury (VILI) de novo. Previous studies have demonstrated that oxidized 1-palmitoyl-2-arachidonoyl- sn -glycero-3-phosphorylcholine (OxPAPC) enhances basal endothelial cell (EC) barrier properties and prevents acute lung inflammation and EC dysfunction in response to bacterial lipopolysaccharide (LPS) via direct Rac-Cdc42-mediated effects on EC cytoskeleton and via competitive inhibition of LPS binding to toll-like receptor 4 (TLR4). Methods: Adult male Brown Norway rats (250-350 g) were ventilated at low tidal volume (LTV, 7 mL/kg) or high tidal volume (HTV, 20 mL/kg) for 2 hours, 85 breaths/min. A subset of animals received intravenous OxPAPC (1.5 mg/kg) at the start of mechanical ventilation. Bronchoalveolar lavage (BAL) cell count and protein concentration were measured as markers of inflammation and vascular permeability. IL-6, IL-1beta, and hyaluronan levels in BAL were quantitatively assessed by enzyme linked immunoabsorbance assays (ELISA). Results: HTV caused a 70% increase in BAL total cell count ( p < .05) and a 169% increase in BAL protein (p < .01) compared with controls. OxPAPC reduced HTV-induced elevations in total cell count (41% decrease versus HTV alone) and protein (42%Abstract : Purpose of Study: Acute lung injury (ALI) is a devastating syndrome characterized by pulmonary inflammation and vascular barrier dysfunction with protein-rich edema. Mechanical ventilation at high tidal volumes can worsen existing ALI and even cause ventilator-induced lung injury (VILI) de novo. Previous studies have demonstrated that oxidized 1-palmitoyl-2-arachidonoyl- sn -glycero-3-phosphorylcholine (OxPAPC) enhances basal endothelial cell (EC) barrier properties and prevents acute lung inflammation and EC dysfunction in response to bacterial lipopolysaccharide (LPS) via direct Rac-Cdc42-mediated effects on EC cytoskeleton and via competitive inhibition of LPS binding to toll-like receptor 4 (TLR4). Methods: Adult male Brown Norway rats (250-350 g) were ventilated at low tidal volume (LTV, 7 mL/kg) or high tidal volume (HTV, 20 mL/kg) for 2 hours, 85 breaths/min. A subset of animals received intravenous OxPAPC (1.5 mg/kg) at the start of mechanical ventilation. Bronchoalveolar lavage (BAL) cell count and protein concentration were measured as markers of inflammation and vascular permeability. IL-6, IL-1beta, and hyaluronan levels in BAL were quantitatively assessed by enzyme linked immunoabsorbance assays (ELISA). Results: HTV caused a 70% increase in BAL total cell count ( p < .05) and a 169% increase in BAL protein (p < .01) compared with controls. OxPAPC reduced HTV-induced elevations in total cell count (41% decrease versus HTV alone) and protein (42% decrease versus HTV alone). HTV also caused an increase in the hyaluronan levels found in BAL samples, which was completely abrogated by intravenous injection of OxPAPC. HTV also caused a 223% increase in the IL-6 levels in BAL samples as compared to controls, which was attenuated by OxPAPC treatment (130% versus control, p < .05). HTV had only a modest effect on IL-1beta up-regulation (45% increase versus control), which still was attenuated by OxPAPC treatment (27% increase versus control). Conclusion: These studies demonstrate for the first time the protective effect of membrane-derived oxidized phospholipids on ventilator-induced lung inflammation and barrier dysfunction. HL75349, HL76259, HL58064. … (more)
- Is Part Of:
- Journal of investigative medicine. Volume 54:Number 2(2006)
- Journal:
- Journal of investigative medicine
- Issue:
- Volume 54:Number 2(2006)
- Issue Display:
- Volume 54, Issue 2 (2006)
- Year:
- 2006
- Volume:
- 54
- Issue:
- 2
- Issue Sort Value:
- 2006-0054-0002-0000
- Page Start:
- S346
- Page End:
- S346
- Publication Date:
- 2006-03-01
- Subjects:
- Clinical medicine -- Periodicals
Medicine -- Research -- Periodicals
Medicine
Research -- United States
Clinical medicine
Medicine -- Research
Periodicals
616.075 - Journal URLs:
- http://journals.lww.com/jinvestigativemed/pages/default.aspx ↗
http://jim.bmj.com/ ↗
https://journals.sagepub.com/home/IMJ ↗
http://journals.lww.com ↗ - DOI:
- 10.2310/6650.2005.x0015.14 ↗
- Languages:
- English
- ISSNs:
- 1081-5589
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - 5008.010000
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