The "in vitro" effects of Dilazep on platelet aggregation and arachidonic acid oxidation in platelets and vessel wall were studied. Dilazep exerted a clearcut inhibitory effect on platelet aggregation induced by several stimuli. In addition, the compound completely suppressed malondialdehyde production by platelets elicited by collagen and thrombin, in a dose-dependent fashion. The evaluation of Dilazep effects on the in vitro release of prostacyclin-like material by rat aortic tissue did not provide any indication about an interference of the drug on the generation of endogenous antiaggregatory material.

Effects of dilazep on human platelets and rat vascular tissue: in vitro studies on platelet aggregation, and arachidonic acid oxidation / S. Colli, P. Maderna, G. Morazzoni, C. Speroni, E. Tremoli. - In: PHARMACOLOGICAL RESEARCH COMMUNICATIONS. - ISSN 0031-6989. - 15:6(1983 Jun), pp. 593-602.

Effects of dilazep on human platelets and rat vascular tissue: in vitro studies on platelet aggregation, and arachidonic acid oxidation

S. Colli
Primo
;
E. Tremoli
Ultimo
1983

Abstract

The "in vitro" effects of Dilazep on platelet aggregation and arachidonic acid oxidation in platelets and vessel wall were studied. Dilazep exerted a clearcut inhibitory effect on platelet aggregation induced by several stimuli. In addition, the compound completely suppressed malondialdehyde production by platelets elicited by collagen and thrombin, in a dose-dependent fashion. The evaluation of Dilazep effects on the in vitro release of prostacyclin-like material by rat aortic tissue did not provide any indication about an interference of the drug on the generation of endogenous antiaggregatory material.
Animals; Aorta; Humans; Blood Vessels; Dilazep; Rats; Arachidonic Acids; Oxidation-Reduction; Platelet Aggregation; Blood Platelets; Azepines; Epoprostenol; Arachidonic Acid; Male; Malondialdehyde
Settore BIO/14 - Farmacologia
giu-1983
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/193666
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