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Possible involvement of eicosanoids in alpha-naphthylthiourea-induced pulmonary oedema and alteration of angiotensin-converting enzyme activity.

Abstract
alpha-Naphthylthiourea (ANTU) when injected intraperitoneally to rats at a dose of 10 mg/kg elicited lung oedema indicated by an increase in lung weight/body weight (LW/BW) ratio and pleural effusion. The injection of acetylsalicylic acid, which is a cyclo-oxygenase inhibitor, and BW 755C, a cyclo-oxygenase and lipoxygenase inhibitor, prior to ANTU produced a significant inhibition in pleural fluid accumulation without changing the LW/BW ratio. BW A4C, a selective 5-lipoxygenase inhibitor, however, caused a highly significant inhibition in pleural effusion and a slight but significant decrease in LW/BW ratio. Thromboxane A2 synthetase inhibitor, UK 38485, caused a slight but significant inhibition in pleural fluid accumulation without altering the LW/BW ratio. Iloprost, however, produced a slight but significant inhibition in the LW/BW ratio without reducing the pleural effusion rate. A significant decrease in angiotensin-converting enzyme (ACE) activity in the isolated perfused lungs of ANTU-treated rats was noted. This observation was thought to be an evidence of a functional alteration of the lung vascular endothelium. The possible role of eicosanoids in lung oedema induced by ANTU and the related mechanisms of decreased ACE activity are discussed.
AuthorsZ S Ercan, S Eren, H Zengil, R K Türker
JournalPharmacology (Pharmacology) Vol. 46 Issue 5 Pg. 274-80 (May 1993) ISSN: 0031-7012 [Print] Switzerland
PMID8387674 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Eicosanoids
  • Peptidyl-Dipeptidase A
  • Thiourea
  • alpha-naphthyl thiourea
Topics
  • Animals
  • Eicosanoids (physiology)
  • Female
  • In Vitro Techniques
  • Lung (drug effects)
  • Male
  • Peptidyl-Dipeptidase A (drug effects, physiology)
  • Perfusion
  • Pulmonary Edema (chemically induced, metabolism)
  • Rats
  • Rats, Inbred Strains
  • Thiourea (analogs & derivatives, pharmacology)

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