Pravastatin Prevents Arrhythmias Induced by Coronary Artery Ischemia/Reperfusion in Anesthetized Normocholesterolemic Rats

ABSTRACT: HMG-CoA reductase inhibitors (statins) have been shown to decrease cardiovascular mortality. Since ventricular tachyarrhythmias are closely related to cardiovascular mortality, we tested effects of the hydrophilic statin pravastatin and the lipophilic statin fluvastatin in a rat arrhythmia...

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Main Authors: Jianguang Chen (Author), Yoshinobu Nagasawa (Author), Bing-Mei Zhu (Author), Masami Ohmori (Author), Ken-ichi Harada (Author), Akio Fujimura (Author), Keitaro Hashimoto (Author)
Format: Book
Published: Elsevier, 2003-01-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Jianguang Chen  |e author 
700 1 0 |a Yoshinobu Nagasawa  |e author 
700 1 0 |a Bing-Mei Zhu  |e author 
700 1 0 |a Masami Ohmori  |e author 
700 1 0 |a Ken-ichi Harada  |e author 
700 1 0 |a Akio Fujimura  |e author 
700 1 0 |a Keitaro Hashimoto  |e author 
245 0 0 |a Pravastatin Prevents Arrhythmias Induced by Coronary Artery Ischemia/Reperfusion in Anesthetized Normocholesterolemic Rats 
260 |b Elsevier,   |c 2003-01-01T00:00:00Z. 
500 |a 1347-8613 
500 |a 10.1254/S1347-8613(19)32620-9 
520 |a ABSTRACT: HMG-CoA reductase inhibitors (statins) have been shown to decrease cardiovascular mortality. Since ventricular tachyarrhythmias are closely related to cardiovascular mortality, we tested effects of the hydrophilic statin pravastatin and the lipophilic statin fluvastatin in a rat arrhythmia model of ischemia/reperfusion and simultaneously measured serum total cholesterol level. Anesthetized rats were subjected to 5-min ischemia and 10-min reperfusion after chronic administration of oral pravastatin (0.02, 0.2, or 2 mg/kg), fluvastatin (0.2, 2, or 4 mg/kg), or vehicle for 22 days, once daily. The acute effect of pravastatin (0.2 or 2 mg/kg, once orally) was also observed. Chronically administrated pravastatin significantly reduced the incidence of ischemia-induced ventricular tachycardia (VT) from 70% (control) to 9% at 2 mg/kg, and it reduced the incidence of reperfusion-induced lethal ventricular fibrillation (VF) from 90% (control) to 20% at 0.2 mg/kg. Acute pravastatin and chronically administrated fluvastatin had no significant effect on these arrhythmias. There were no significant changes in blood pressure, heart rate, QT interval, and serum cholesterol among pravastatin-, fluvastatin-, and vehicle-treated groups. Hydrophilic pravastatin prevented reperfusion-induced lethal VF in anesthetized rats by chronic administration independent of its cholesterol lowering effect. This may be a new beneficial role of pravastatin in decreasing cardiovascular mortality. 
546 |a EN 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Journal of Pharmacological Sciences, Vol 93, Iss 1, Pp 87-94 (2003) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S1347861319326209 
787 0 |n https://doaj.org/toc/1347-8613 
856 4 1 |u https://doaj.org/article/f15252e4fac44f268e93ac94a596c24c  |z Connect to this object online.