Kirk R G, Lee P, Reasor M J
Department of Anatomy, West Virginia University Health Sciences Center, Morgantown 26506.
Exp Mol Pathol. 1990 Feb;52(1):122-31. doi: 10.1016/0014-4800(90)90064-k.
Treatment with the iodine-containing antiarrhythmic drug, amiodarone, can cause pulmonary toxicity. Alveolar macrophages are particularly susceptible to formation of lipidrich lamellar bodies in amiodarone-treated animals. Amiodarone and several of its metabolites accumulate in the cell. Previously, we have reported that the technique of X-ray microanalysis is useful in monitoring the distribution of iodine in freeze-dried cryosections of alveolar macrophages from Fischer 344 rats 24 hr after a single dose of amiodarone. In the present study, we examine the effects of longer term amiodarone treatment of 1 or 9 weeks. Substantial changes in iodine distribution occur in the cells with increasing length of drug treatment. High concentrations of iodine are found early in the lamellar bodies. The iodine levels in the nuclei slowly increase with the length of treatment, and after 9 weeks of treatment, approach those found in the lamellar bodies. It is possible that this accumulation of iodine in the nuclei is due to the presence of polar metabolites. In addition, the potassium concentration in the cell decreases and the sodium increases with treatment duration. These changes in cations are most likely due to altered ion transport in the macrophages by the inhibition of membrane Na-K-ATPase by the drug and its principal metabolite, desethylamiodarone.
使用含碘抗心律失常药物胺碘酮进行治疗可能会导致肺部毒性。在接受胺碘酮治疗的动物中,肺泡巨噬细胞特别容易形成富含脂质的板层小体。胺碘酮及其几种代谢产物会在细胞中蓄积。此前,我们曾报道,X射线微量分析技术有助于监测单次给予胺碘酮24小时后Fischer 344大鼠肺泡巨噬细胞冻干冰冻切片中碘的分布情况。在本研究中,我们考察了为期1周或9周的长期胺碘酮治疗的效果。随着药物治疗时间的延长,细胞内碘的分布发生了显著变化。在板层小体中早期就发现了高浓度的碘。细胞核中的碘水平随着治疗时间的延长而缓慢升高,在治疗9周后,接近在板层小体中发现的水平。细胞核中碘的这种蓄积可能是由于极性代谢产物的存在。此外,随着治疗时间的延长,细胞内钾浓度降低而钠浓度升高。这些阳离子的变化很可能是由于药物及其主要代谢产物去乙基胺碘酮对膜Na-K-ATP酶的抑制作用,导致巨噬细胞中离子转运发生改变所致。