Nicolay Jan P, Bentzen Peter J, Ghashghaeinia Mehrdad, Wieder Thomas, Lang Florian
Department of Physiology, University of Tübingen, Germany.
Cell Physiol Biochem. 2007;20(6):1043-50. doi: 10.1159/000110713. Epub 2007 Oct 30.
Side effects of amiodarone, an effective antiarrhythmic drug, include anemia, which may be caused by decreased formation or accelerated death of erythrocytes. Suicidal erythrocyte death (eryptosis) is characterized by cell shrinkage and cell membrane scrambling leading to phosphatidylserine exposure at the cell surface. Stimulators of erythrocyte membrane scrambling include increase of cytosolic Ca2+ concentration ([Ca2+]i) following activation of Ca2+-permeable cation channels. Moreover, eryptosis is triggered by ceramide. The present study has been performed to test for an effect of amiodarone on eryptosis. Erythrocytes from healthy volunteers were exposed to amiodarone and phosphatidylserine exposure (annexin V binding), cell volume (forward scatter), [Ca2+]i (Fluo3-dependent fluorescence), and ceramide formation (anti-ceramide-FITC antibody and radioactive labelling) determined by flow cytometry. Exposure of erythrocytes to amiodarone (1 microM) increased [Ca2+]i and triggered annexin V binding, but did not significantly decrease forward scatter and did not significantly influence ceramide formation. Amiodarone augmented the increase of annexin binding following hypertonic shock (addition of 550 mM sucrose) but did not significantly alter the enhanced annexin binding following Cl- removal (replacement with gluconate). Amiodarone did not significantly modify the decrease of forward scatter following hypertonic shock or Cl- removal. The present observations disclose a novel action of amiodarone which may contribute to the side effects of the drug.
胺碘酮是一种有效的抗心律失常药物,其副作用包括贫血,这可能是由红细胞生成减少或死亡加速所致。自杀性红细胞死亡(eryptosis)的特征是细胞萎缩和细胞膜磷脂酰丝氨酸外翻,导致磷脂酰丝氨酸暴露于细胞表面。红细胞膜磷脂酰丝氨酸外翻的刺激因素包括钙通透性阳离子通道激活后胞质Ca2+浓度([Ca2+]i)升高。此外,神经酰胺可引发eryptosis。本研究旨在测试胺碘酮对eryptosis的影响。将健康志愿者的红细胞暴露于胺碘酮中,通过流式细胞术测定磷脂酰丝氨酸暴露(膜联蛋白V结合)、细胞体积(前向散射)、[Ca2+]i(基于Fluo3的荧光)和神经酰胺形成(抗神经酰胺-FITC抗体和放射性标记)。将红细胞暴露于胺碘酮(1μM)可使[Ca2+]i升高并引发膜联蛋白V结合,但未显著降低前向散射,也未显著影响神经酰胺形成。胺碘酮增强了高渗休克(添加550 mM蔗糖)后膜联蛋白结合的增加,但对去除Cl-(用葡萄糖酸盐替代)后增强的膜联蛋白结合无显著影响。胺碘酮对高渗休克或去除Cl-后前向散射的降低无显著改变。本观察结果揭示了胺碘酮的一种新作用,这可能与该药物的副作用有关。