Mitochondrial CYP2E1 is sufficient to mediate oxidative stress and cytotoxicity induced by ethanol and acetaminophen

L Knockaert, V Descatoire, N Vadrot, B Fromenty… - Toxicology in Vitro, 2011 - Elsevier
Several cytochromes P450 (CYPs) are not only located in the endoplasmic reticulum but
also within mitochondria. One such CYP is CYP2E1 which metabolizes numerous …

Comparative evaluation of amiodarone-induced phospholipidosis and drug accumulation in Fischer-344 and Sprague-Dawley rats

MJ Reasor, CM McCloud, TL Beard, DC Ebert… - Toxicology, 1996 - Elsevier
Amiodarone (AD) and its major metabolite, desethylamiodarone (desethylAD), are both
phospholipogenic. The present study was undertaken to evaluate the comparative …

Vitamin E reduces accumulation of amiodarone and desethylamiodarone and inhibits phospholipidosis in cultured human cells

UE Honegger, I Scuntaro, UN Wiesmann - Biochemical pharmacology, 1995 - Elsevier
Chronic administration of amiodarone (AMIO), widely used by clinicians for the treatment of
therapy-resistant cardiac arrhythmias, is frequently associated with serious side-effects …

Attenuation of amiodarone-induced pulmonary fibrosis by vitamin E is associated with suppression of transforming growth factor-β1 gene expression but not …

JW Card, WJ Racz, JF Brien, TE Massey - Journal of Pharmacology and …, 2003 - ASPET
Amiodarone (AM) is an efficacious antidysrhythmic agent that can cause numerous adverse
effects, including potentially life-threatening pulmonary fibrosis. The current study was …

Effects of vitamin E on cytotoxicity of amiodarone and N-desethylamiodarone in isolated hamster lung cells

MW Bolt, WJ Racz, JF Brien, TE Massey - Toxicology, 2001 - Elsevier
Amiodarone (AM) is a potent and efficacious antidysrhythmic agent that can cause
potentially life-threatening pulmonary fibrosis. Vitamin E has been demonstrated to …

Amiodarone: ionic and cellular mechanisms of action of the most promising class III agent

I Kodama, K Kamiya, J Toyama - The American journal of cardiology, 1999 - Elsevier
Amiodarone is the most promising drug in the treatment of life-threatening ventricular
tachyarrhythmias in patients with significant structural heart disease. The pharmacologic …

DNA damage‐induced apoptosis and mitogen‐activated protein kinase pathway contribute to the toxicity of dronedarone in hepatic cells

S Chen, Z Ren, D Yu, B Ning… - Environmental and …, 2018 - Wiley Online Library
Dronedarone, an antiarrhythmic drug, has been marketed as an alternative to amiodarone.
The use of dronedarone has been associated with severe liver injury; however, the …

Severe intrahepatic cholestasis caused by amiodarone toxicity after withdrawal of the drug: a case report and review of the literature

CC Chang, M Petrelli… - … of Pathology and …, 1999 - meridian.allenpress.com
Cholestasis has been reported as a rare presentation among patients with severe liver injury
secondary to amiodarone hepatic toxicity. We report an unusual case of amiodarone …

Cyclosporine A protects against arachidonic acid toxicity in rat hepatocytes: role of CYP2E1 and mitochondria

D Wu, AI Cederbaum - Hepatology, 2002 - journals.lww.com
Diets high in polyunsaturated fatty acids (PUFA) are important for the development of
alcoholic liver injury. The goal of this report was to characterize toxicity by arachidonic acid …

Cellular accumulation of amiodarone and desethylamiodarone in cultured human cells: Consequences of drug accumulation on cellular lipid metabolism and plasma …

UE Honegger, RD Zuehlke, I Scuntaro… - Biochemical …, 1993 - Elsevier
Amiodarone (AMIO), a potent antiarrhythmic drug, is clinically widely used despite its
frequent side effects after chronic administration. These side effects coincide with an …