Capecchi P L, Laghi Pasini F, Ceccatelli L, Di Perri T
Institute of Clinical Medicine, University of Siena School of Medicine, Policlinico Le Scotte, Italy.
Immunopharmacol Immunotoxicol. 1993 Mar-Jun;15(2-3):133-49. doi: 10.3109/08923979309025990.
The dihydropyridine derivative isradipine is able to inhibit PMN leukocyte function, such as enzyme release and free radical generation, following the activation with specific stimuli. Moreover, the drug prevents calcium influx into the cells as detected by the specific fluorescent dye FURA 2/acetoxymethylester. The specific adenosine receptor antagonist theophylline is able to partially remove the inhibiting activity, thus suggesting a possible interference of isradipine with the adenosine system. Such a cell-protecting activity adds further rationale to the employment of isradipine in those conditions, such as acute and chronic ischaemia and reperfusion damage, in which PMN leukocyte-dependent tissue injury represents a relevant pathogenetic mechanism.
二氢吡啶衍生物伊拉地平能够抑制多形核白细胞(PMN)的功能,如在特定刺激激活后酶的释放和自由基的产生。此外,用特异性荧光染料FURA 2/乙酰氧基甲酯检测发现,该药物可阻止钙流入细胞。特异性腺苷受体拮抗剂茶碱能够部分消除这种抑制活性,从而提示伊拉地平可能与腺苷系统存在相互作用。这种细胞保护活性为伊拉地平在诸如急性和慢性缺血及再灌注损伤等情况下的应用提供了进一步的理论依据,在这些情况下,PMN白细胞依赖性组织损伤是一种相关的致病机制。