Fernandes P D, Assreuy J
Departamento de Farmacologia Básica e Clínica, Universidade Federal do Rio de Janeiro, Brasil.
Braz J Med Biol Res. 1997 Jan;30(1):93-9. doi: 10.1590/s0100-879x1997000100015.
Giardia lamblia trophozoites were incubated for 2 h with activated murine macrophages, nitric oxide (NO) donors or a superoxide anion generator (20 mU/ml xanthine oxidase plus 1 mM xanthine). Activated macrophages were cytotoxic to Giardia trophozoites (approximately 60% dead trophozoites). The effect was inhibited (> 90%) by an NO synthase inhibitor (200 microM) and unaffected by superoxide dismutase (SOD, 300 U/ml). Giardia trophozoites were killed by the NO donors, S-nitroso-acetyl-penicillamine (SNAP) and sodium nitroprusside (SNP) in a dose-dependent manner (LD50 300 and 50 microM, respectively). A dual NO-superoxide anion donor, 3-morpholino-sydnonimine hydrochloride (SIN-1), did not have a killing effect in concentrations up to 1 mM. However, when SOD (300 U/ml) was added simultaneously with SIN-1 to Giardia, a significant trophozoite-killing effect was observed (approximately 35% dead trophozoites at 1 mM). The mixtures of SNAP or SNP with superoxide anion, which yields peroxynitrite, abolished the trophozoite killing induced by NO donors. Authentic peroxynitrite only killed trophozoites at very high concentrations (3 mM). These results indicate that NO accounts for Giardia trophozoites killing and this effect is not mediated by peroxynitrite.
将贾第虫滋养体与活化的小鼠巨噬细胞、一氧化氮(NO)供体或超氧阴离子生成剂(20 mU/ml黄嘌呤氧化酶加1 mM黄嘌呤)孵育2小时。活化的巨噬细胞对贾第虫滋养体具有细胞毒性(约60%的滋养体死亡)。这种作用被NO合酶抑制剂(200 microM)抑制(>90%),且不受超氧化物歧化酶(SOD,300 U/ml)影响。贾第虫滋养体被NO供体、S-亚硝基乙酰青霉胺(SNAP)和硝普钠(SNP)以剂量依赖方式杀死(LD50分别为300和50 microM)。双NO-超氧阴离子供体3-吗啉代西多硝胺盐酸盐(SIN-1)在浓度高达1 mM时没有杀伤作用。然而,当SOD(300 U/ml)与SIN-1同时加入贾第虫时,观察到显著的滋养体杀伤作用(1 mM时约35%的滋养体死亡)。SNAP或SNP与超氧阴离子的混合物可产生过氧亚硝酸盐,消除了NO供体诱导的滋养体杀伤作用。纯过氧亚硝酸盐仅在非常高的浓度(3 mM)下杀死滋养体。这些结果表明,NO是导致贾第虫滋养体死亡的原因,且这种作用不是由过氧亚硝酸盐介导的。