Sánchez Gregorio Martínez, Rodríguez H María A, Giuliani Attilia, Núñez Sellés Alberto J, Rodríguez Niurka Pons, León Fernández Olga Sonia, Re L
Centre for Research and Biological Evaluation, Pharmacy Institute, Havana University, San Lazaro y L, Havana 4, Cuba.
Phytother Res. 2003 Mar;17(3):197-201. doi: 10.1002/ptr.921.
The effect of Mangifera indica L. extract (Vimang) on treatment of injury associated with hepatic ischaemia/reperfusion was tested. Vimang protects from the oxidative damage induced by oxygen-based free radicals as shown in several in vitro test systems conducted. The ability of Vimang to reduce liver damage was investigated in rats undergoing right-lobe blood fl ow occlusion for 45 min followed by 45 min of reperfusion. The ischaemia/reperfusion model leads to an increase of transaminase (ALT and AST), membrane lipid peroxidation, tissue neutrophil in filtration, DNA fragmentation, loss of protein -SH groups, cytosolic Ca2+ overload and a decrease of catalase activity. Oral administration of Vimang (50, 110 and 250 mg/kg, b.w.) 7 days before reperfusion, reduced transaminase levels and DNA fragmentation in a dose dependent manner (p < 0.05). Vimang also restored the cytosolic Ca2+ levels and inhibited polymorphonuclear migration at a dose of 250 mg/kg b.w., improved the oxidation of total and non protein sulfhydryl groups and prevented modification in catalase activity, uric acid and lipid peroxidation markers (p < 0.05). These data suggest that Vimang could be a useful new natural drug for preventing oxidative damage during hepatic injury associated with free radical generation.
测试了芒果提取物(Vimang)对治疗肝缺血/再灌注相关损伤的效果。如在多个体外测试系统中所示,Vimang可保护免受氧自由基诱导的氧化损伤。在经历右叶血流阻断45分钟后再灌注45分钟的大鼠中研究了Vimang减轻肝损伤的能力。缺血/再灌注模型导致转氨酶(ALT和AST)升高、膜脂质过氧化、组织中性粒细胞浸润、DNA片段化、蛋白质-SH基团丢失、胞质Ca2+过载以及过氧化氢酶活性降低。在再灌注前7天口服Vimang(50、110和250mg/kg,体重),以剂量依赖方式降低转氨酶水平和DNA片段化(p<0.05)。Vimang还能恢复胞质Ca2+水平,并以250mg/kg体重的剂量抑制多形核白细胞迁移,改善总巯基和非蛋白质巯基的氧化,并防止过氧化氢酶活性、尿酸和脂质过氧化标志物的改变(p<0.05)。这些数据表明,Vimang可能是一种有用的新型天然药物,可预防与自由基产生相关的肝损伤期间的氧化损伤。