The eects of amiodarone (AMD) on lipid peroxidation of rat liver mitochondria, the formation of superoxide anions at the respiratory chain level, and the cytosolic and mitochondrial enzymatic protective mechanisms of oxidative stress were studied. An attempt of classify AMD according to its toxic ab
Neutrality of amiodarone on the initiation and propagation of membrane lipid peroxidation
✍ Scribed by Fabiana Postiglione Mansani; Teresa C. P. Dinis; Eva Gunilla Skare Carnieri; Vítor M. C. Madeira
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 178 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0263-6484
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✦ Synopsis
Amiodarone is an iodinated benzofuran derivative largely used as an antiarrhythmic. Owing to the sensitivity of heart tissue to radicals, amiodarone was assayed for putative eects on lipid peroxidation studied in liposomes of soybean phosphatidylcholine and of bovine heart mitochondrial lipids used as model systems. Lipid peroxidations were initiated with Fe 2 /ascorbic acid, and with peroxyl radicals generated from the azocompounds, AAPH and AMVN. These assays were carried out by following the quenching of the ¯uorescent probe cis-parinaric acid and by monitoring oxygen consumption. It has been ascertained that amiodarone does not protect or potentiate signi®cantly the lipid peroxidation in both lipidic systems. To fully ascertain the neutral behaviour of amiodarone in the lipid peroxidation process, the degradation of phospholipid acyl chains has been checked by GLC. These data con®rm that amiodarone does not protect or potentiate lipid peroxidation to a signi®cant extent. It is concluded that the limited eects of amiodarone might be related only indirectly with the lipid peroxidation. It is possible that the drug causes limited conformational and biophysical alterations in membrane phospholipid bilayers that can aect the process of peroxidation. Therefore, it is concluded that the therapeutic eects and bene®ts as a heart antiarrhythmic agent are independent of lipid peroxidation processes. Furthermore, the interaction of the drug with lipid bilayers does not induce signi®cant conformational perturbations that could signi®cantly favour or depress the peroxidation process.
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