2016
DOI: 10.1016/j.ejps.2015.10.002
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Characterization of Disopyramide derivative ADD424042 as a non-cardiotoxic neuronal sodium channel blocker with broad-spectrum anticonvulsant activity in rodent seizure models

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Cited by 8 publications
(2 citation statements)
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“…A number of studies have shown that cardiotoxic drugs prolong QT interval in rodents, and ECG recording in rats has been used as a screening tool in cardiotoxicity studies (Hanada et al 1999, Ohtani et al 1996, Król et al 2016. However, it needs to be stressed that the translation of the results of those studies to humans has limitations.…”
Section: Qt Intervalmentioning
confidence: 99%
“…A number of studies have shown that cardiotoxic drugs prolong QT interval in rodents, and ECG recording in rats has been used as a screening tool in cardiotoxicity studies (Hanada et al 1999, Ohtani et al 1996, Król et al 2016. However, it needs to be stressed that the translation of the results of those studies to humans has limitations.…”
Section: Qt Intervalmentioning
confidence: 99%
“…From the result obtained in this study, severe hypotension associated with Isoproterenol-induced myocardial injury can be linked with cardiac output and peripheral resistance alteration. The cardiac output was altered, probably due to increased myocardial oxygen consumption arising from larger dose of Isoproterenol which possess higher affinity for β 1 and β 2 receptor of the myocardial tissue [36] leading to imbalance between cardiac muscle workload and oxygen supply [37]. This is associated with tachycardia, thereby reducing the ventricular filling time of the diastolic phase during cardiac cycle, leading to low stroke volume/ejection fraction and reduced cardiac output.…”
Section: Discussionmentioning
confidence: 99%