Abstract |
The present study was undertaken to investigate the involvement of PAF in acute pancreatitis induced by cerulein in rats. Cerulein (two doses of 20 micrograms/rat, the first s.c. and the second i.v., 1 h apart) induced a significant increase in vascular permeability in the pancreas, evaluated by the Evans blue (EB) extravasation method. Plasma amylase levels were also significantly increased in this group. The PAF antagonists, BN-52021 (5 mg/kg) and WEB-2170 (1 and 10 mg/kg), both significantly reduced the extravasation of EB in the pancrease induced by i.v. injection of PAF (1 microgram/kg). At these concentrations, BN-52021 was effective at inhibiting cerulein-induced pancreatitis (60-70% of inhibition) whereas WEB-2170 had no significant effect. Although the inhibition induced by BN-52021 suggests the involvement of PAF in cerulein- pancreatitis, the lack of effect of WEB-2170 reported here does not allow a definite conclusion. Further studies are needed to elucidate the differential effect of the PAF antagonists.
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Authors | S Jancar, E E Abdo, S N Sampietre, F H Kwasniewski, A M Coelho, A Bonizzia, M C Machado |
Journal | Journal of lipid mediators and cell signalling
(J Lipid Mediat Cell Signal)
Vol. 11
Issue 1
Pg. 41-9
(Jan 1995)
ISSN: 0929-7855 [Print] Netherlands |
PMID | 7537159
(Publication Type: Comparative Study, Journal Article)
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Chemical References |
- Azepines
- Diterpenes
- Ginkgolides
- Lactones
- Platelet Activating Factor
- Triazoles
- Evans Blue
- Ceruletide
- bepafant
- ginkgolide B
- Amylases
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Topics |
- Acute Disease
- Amylases
(blood)
- Animals
- Azepines
(pharmacology)
- Capillary Permeability
(drug effects)
- Ceruletide
(toxicity)
- Diterpenes
- Evans Blue
(pharmacokinetics)
- Ginkgolides
- Lactones
(pharmacology)
- Male
- Pancreas
(blood supply)
- Pancreatitis
(chemically induced, drug therapy, enzymology)
- Platelet Activating Factor
(antagonists & inhibitors)
- Rats
- Rats, Wistar
- Triazoles
(pharmacology)
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