Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/12924
Title: Interaction of diclofenac and ketoprofen with cardioactive drugs in rats
Authors: Vida Jakovljević
Ana Sabo 
Zdenko Tomić 
Boris Milijašević 
Mira Popović
Velibor Vasović 
Aleksandar Rašković 
Keywords: Diclofenac;ketoprofen;cardiosensitivity
Issue Date: 1-Jan-2009
Journal: European Journal of Drug Metabolism and Pharmacokinetics
Abstract: The interaction of diclofenac and ketoprofen, both applied intraperitoneally in a dose of 8 mg/kg for twenty-eight days, was assessed with cardioactive drugs in rats. Interaction was assessed on the basis of ECG records after the infusion of adrenaline, verapamil or lidocaine to the rats treated with diclofenac or ketoprofen vs control. The infusion time was measured in seconds to the moment of the appearance of the first heart reaction to the infusion of the cardioactive drug, then to the appearance of more frequent changes in the ECG record, and finally, to the occurrence of the toxic effect. It was also measured the plasma concentrations of sodium and potassium ions. As well as diclofenac and ketoprofen concentration, 2 hours after single and 28th dose. ECG patterns revealed no occurrence of cardiotoxic action of diclofenac and ketoprofen. The treatment with diclofenac caused significantly lower sodium plasma concentrations whereas the concentration of potassium was increased. Diclofenac concentrations were the same after a single and multiple doses, whereas concentrations of ketoprofen were significantly higher after a single dose than after its multiple applications.
URI: https://open.uns.ac.rs/handle/123456789/12924
ISSN: 3787966
DOI: 10.1007/BF03191378
Appears in Collections:MDF Publikacije/Publications

Show full item record

SCOPUSTM   
Citations

3
checked on May 10, 2024

Page view(s)

33
Last Week
10
Last month
0
checked on May 10, 2024

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.