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Pharmacological manipulation of inflammation in rabbit hydronephrosis: effects of a combined cyclooxygenase/lipoxygenase inhibitor ethoxyquin, a thromboxane synthase inhibitor RS-5186 and a PAF antagonist L-659,989.

Abstract
The rabbit hydronephrotic kidney (HNK) is a model of renal inflammation characterized by a marked increase in arachidonic acid metabolism that is temporally associated with an inflammatory cell influx into the injured tissue. The HNK exhibits an exaggerated elaboration of eicosanoids ex vivo in response to either bradykinin or the inflammatory cell agonist n-formyl-methionyl-leucyl-phenylalanine (fMLP) compared with the unobstructed contralateral kidney. To pharmacologically manipulate inflammatory cell influx into the HNK we administered ethoxyquin (200 mg/kg p.o.), a combined cyclooxygenase/lipoxygenase inhibitor, RS-5186 (10 mg/kg p.o.), a thromboxane synthase inhibitor or L-659,989 (5 mg/kg p.o.), a platelet activating factor antagonist, before and at various times during the development of hydronephrosis. Only ethoxyquin reduced inflammatory cell influx into the HNK and thereby prevented the enhancement of microsomal cyclooxygenase activity and attenuated the elaboration of eicosanoids ex vivo. Collectively, these results suggest a primary role of an eicosanoid, possibly leukotriene B4, but not thromboxane A2 or the chemotactic phospholipid, platelet activating factor, as a mediator of inflammatory cell influx resulting from ureter obstruction.
AuthorsS M Spaethe, W Hsueh, P Needleman
JournalThe Journal of pharmacology and experimental therapeutics (J Pharmacol Exp Ther) Vol. 248 Issue 3 Pg. 1308-16 (Mar 1989) ISSN: 0022-3565 [Print] United States
PMID2539462 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Arachidonic Acids
  • Cyclooxygenase Inhibitors
  • Fatty Acids, Nonesterified
  • Furans
  • Lipoxygenase Inhibitors
  • Platelet Activating Factor
  • Quinolines
  • Thiophenes
  • RS 5186
  • L 659989
  • Leukotriene B4
  • Arachidonic Acid
  • Ethoxyquin
  • Thromboxane-A Synthase
Topics
  • Animals
  • Arachidonic Acid
  • Arachidonic Acids (metabolism)
  • Cyclooxygenase Inhibitors
  • Ethoxyquin (pharmacology)
  • Fatty Acids, Nonesterified (deficiency)
  • Furans (pharmacology)
  • Hydronephrosis (metabolism, pathology)
  • Inflammation (drug therapy)
  • Kidney (drug effects, metabolism)
  • Leukotriene B4 (physiology)
  • Lipoxygenase Inhibitors
  • Male
  • Perfusion
  • Platelet Activating Factor (antagonists & inhibitors)
  • Quinolines (pharmacology)
  • Rabbits
  • Thiophenes (pharmacology)
  • Thromboxane-A Synthase (antagonists & inhibitors)

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