Title of article :
Immunohistochemical evidence for involvement of inflammatory cytokines in anti-arrhythmic effects of rosuvastatin in male rats
Author/Authors :
Amini, Sima Department of Pharmacology - Tehran University of Medical Sciences, Tehran, Iran , Nikoui, Vahid Razi Drug Research Center - Iran University of Medical Sciences, Tehran, Iran , Jazaeri, Farahnaz Department of Pharmacology - Tehran University of Medical Sciences, Tehran, Iran , Imran Khan, Muhammad Department of Pharmacy - Kohat University of Science and Technology, Kohat, Pakistan , Partoazar, Alireza Experimental Medicine Research Center - Tehran University of Medical Sciences, Tehran, Iran , Bakhtiarian, Azam Department of Pharmacology - Tehran University of Medical Sciences, Tehran, Iran
Pages :
10
From page :
142
To page :
151
Abstract :
Introduction: Considering the cardioprotective and anti-inflammatory properties of statins, the aim of the present experiment was to investigate the possible involvement of inflammatory cytokines in anti-arrhythmic effects of rosuvastatin in both in vitro and in vivo experiments in rats. Methods: Three weeks after oral administration of either of rosuvastatin or vehicle, the atria were removed and after incubation with ouabain, time of onset of arrhythmia and asystole were recorded. We also used immunohistochemistry technique to identify the differentially expressed proteins interleukin (IL)-1β, IL-6 and tumor necrosis factor (TNF)-α in atria. Results: Rosuvastatin significantly postponed the onset of arrhythmia compared to vehicle-treated group. Injection of ouabain increased the atrial expression of IL-1β, IL-6 and TNF-α proteins, while pretreatment of rats with rosuvastatin could significantly attenuate them. Conclusion: Our data suggest that rosuvastatin exerts anti-arrhythmic properties at least in part through modulation of inflammatory cytokines.
Keywords :
Rosuvastatin , Cardiovascular , Arrhythmia , Inflammatory cytokines
Journal title :
Physiology and Pharmacology
Serial Year :
2020
Record number :
2522539
Link To Document :
بازگشت