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Suppressive effect of prostaglandin E1 on pulmonary hypertension induced by monocrotaline in rats.

Abstract
The effect of administering prostaglandin E1 (PGE1) on the extent of monocrotaline (MCT)-induced pulmonary hypertension and cytokine production [interleukins (IL) 1 and 6 and tumor necrosis factor (TNF)] by macrophages during MCT induction of pulmonary hypertension was studied. Right ventricle/left ventricle plus septum weight ratios (RV/LV + S) were used as an index of the development of pulmonary hypertension. Administering PGE1 at a dose of 0.2 mg/kg/day for 4 weeks reduced significantly the RV/LV + S ratio from 0.428 +/- 0.070 to 0.243 +/- 0.059 (p < 0.01) and decreased the production of these cytokines: IL-1, from 4.675 +/- 3.558 to 1.800 +/- 0.722 units; IL-6, from 0.322 +/- 0.121 to 0.060 +/- 0.039 units; and TNF, from 0.578 +/- 0.369 to 0.004 +/- 0.004 units. In another series of experiments, a significant reduction of the RV/LV + S ratio was noted for only 1 week when we administered PGE1 immediately after the injection of MCT. We confirmed that histopathologic improvements of lungs were noted by administering 0. 2 mg/kg PGE1 for 4 weeks. In another experiment, PGE1 at a concentration of 2 microg/ml suppressed a rise in the cytosolic Ca2+ concentration of lipopolysaccharide-stimulated peritoneal macrophages of rats in vitro, suggesting that PGE1 suppressed cytokine production by macrophages through the suppression of the Ca2+ influx. These results suggest that administering PGE1 may be effective in the treatment of some forms of pulmonary hypertension in humans.
AuthorsF Sakuma, M Miyata, R Kasukawa
JournalLung (Lung) Vol. 177 Issue 2 Pg. 77-88 ( 1999) ISSN: 0341-2040 [Print] United States
PMID9929405 (Publication Type: Journal Article)
Chemical References
  • Cytokines
  • Monocrotaline
  • Alprostadil
  • Calcium
Topics
  • Alprostadil (pharmacology)
  • Animals
  • Calcium (metabolism)
  • Cytokines (blood)
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Heart Septum (pathology)
  • Heart Ventricles (pathology)
  • Hypertension, Pulmonary (chemically induced, pathology, physiopathology)
  • Macrophages, Alveolar (drug effects, pathology)
  • Male
  • Monocrotaline
  • Pulmonary Wedge Pressure (drug effects, physiology)
  • Rats
  • Rats, Sprague-Dawley

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