Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

Dembinska-Kiec, A; Peskar, BA; Muller, MK; Peskar, BM.
The effects of platelet-activating factor on flow rate and eicosanoid release in the isolated perfused rat gastric vascular bed.
Prostaglandins. 1989; 37(1):69-91 Doi: 10.1016/0090-6980(89)90033-6
Web of Science PubMed FullText FullText_MUG Google Scholar

 

Co-Autor*innen der Med Uni Graz
Peskar Bernhard
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
In the isolated rat stomach perfused via the vasculature in situ under constant pressure bolus injections of platelet-activating factor (PAF, 3, 16, or 50 ng) induced dose-dependent, long-lasting reductions of flow rates and simultaneously significant increases in the release of cysteinyl-leukotrienes (cys-LT), thromboxane (TX) B2 and 6-keto-prostaglandin (PG) F1 alpha. Reversed phase high pressure liquid chromatography demonstrated the release of a mixture of comparable amounts of LTC4, LTD4 and LTE4 by PAF. Inhibition of cys-LT synthesis by the lipoxygenase inhibitors nordihydroguaiaretic acid (NDGA) and L-651,896 did not significantly affect PAF-induced flow reduction indicating that endogenous cys-LT are of minor importance for the PAF effect on gastric vascular flow. This conclusion is supported by the fact that the cys-LT receptor antagonist FPL 55712 in a concentration (1 x 10(-6) M) that completely antagonized gastric flow reduction by exogenous LTC4 (1 x 10(-7) M) had no effect on the PAF-induced reduction of flow. The cyclooxygenase inhibitor indomethacin aggravated the PAF-induced flow reduction suggesting that the endogenous vasodilator PGI2 might act as a functional PAF antagonist in the rat gastric vascular bed. In contrast to FPL 55712 the PAF antagonist BN 52021 significantly and concentration-dependently antagonized the PAF effect on gastric vascular flow. The results demonstrate that PAF and LTC4 induce flow reductions in the rat gastric vascular bed by activating different receptors and that endogenous eicosanoids released by PAF do not contribute significantly to the PAF effect on gastric vascular flow.
Find related publications in this database (using NLM MeSH Indexing)
6-Ketoprostaglandin F1 alpha - metabolism
Animals - metabolism
Arachidonate 5-Lipoxygenase - antagonists and inhibitors
Benzofurans - pharmacology
Blood Flow Velocity - pharmacology
Chromatography, High Pressure Liquid - pharmacology
Chromones - pharmacology
Diterpenes - pharmacology
Ginkgolides - pharmacology
Indomethacin - pharmacology
Lactones - pharmacology
Male - pharmacology
Nordihydroguaiaretic Acid - pharmacology
Platelet Activating Factor - antagonists and inhibitors
Rats - antagonists and inhibitors
Rats, Inbred Strains - antagonists and inhibitors
SRS-A - antagonists and inhibitors
Stomach - blood supply
Thromboxane B2 - metabolism

© Med Uni Graz Impressum