Altunoluk Bulent, Soylemez Haluk, Oguz Fatih, Turkmen Emine, Fadillioglu Ersin
Department of Physiology, Faculty of Medicine, Hacettepe University, Ankara 06100, Turkey.
Ann Clin Lab Sci. 2006 Summer;36(3):326-32.
Zofenopril ameliorates experimental cardiac ischemia/reperfusion (IR) injury in animal models and exhibits beneficial cardiovascular effects in patients with myocardial infarction. The objective of the present research was to investigate whether zofenopril can protect against renal IR injury. Rats were divided into 4 experimental groups: (a) control, (b) IR (60 min of ischemia followed by 24 hr of reperfusion), (c) zofenopril (15 mg/kg/day for 2 days), and (d) zofenopril+IR. All of the rats underwent right nephrectomy, and the rats in the IR and zofenopril+IR groups also underwent IR.then the left kidneys were removed for biochemical analyses and microscopic examination. There were no abnormalities in the biochemical and microscopic findings in the preoperative right kidneys. The lipid peroxidation, protein oxidation, and nitric oxide levels as well as xanthine oxidase and myeloperoxidase activities were increased and the catalase and superoxide dismutase activities were decreased in the IR group; zofenopril treatment prevented these changes (p <0.05). In the IR group, the kidney sections showed severe acute tubular damage including brush border loss, nuclear condensation, cytoplasmic swelling, and loss of nuclei; in the zofenopril+IR group, the normal glomerular morphology was preserved and there was slight edema of the tubular cells. The renal damage score was significantly reduced in the zofenopril+IR group vs the IR group (p <0.05). In conclusion, IR injury caused oxidative damage in renal tissue and zofenopril prevented this IR injury.
佐芬普利可改善动物模型中的实验性心脏缺血/再灌注(IR)损伤,并对心肌梗死患者具有有益的心血管效应。本研究的目的是调查佐芬普利是否能预防肾IR损伤。将大鼠分为4个实验组:(a)对照组,(b)IR组(缺血60分钟后再灌注24小时),(c)佐芬普利组(15毫克/千克/天,共2天),以及(d)佐芬普利+IR组。所有大鼠均接受右肾切除术,IR组和佐芬普利+IR组的大鼠还接受了IR处理。然后取出左肾进行生化分析和显微镜检查。术前右肾的生化和显微镜检查结果均无异常。IR组的脂质过氧化、蛋白质氧化和一氧化氮水平以及黄嘌呤氧化酶和髓过氧化物酶活性增加,而过氧化氢酶和超氧化物歧化酶活性降低;佐芬普利治疗可防止这些变化(p<0.05)。在IR组中,肾切片显示严重的急性肾小管损伤,包括刷状缘丧失、核浓缩、细胞质肿胀和细胞核丢失;在佐芬普利+IR组中,肾小球形态正常,肾小管细胞有轻微水肿。佐芬普利+IR组的肾损伤评分显著低于IR组(p<0.05)。总之,IR损伤导致肾组织氧化损伤,而佐芬普利可预防这种IR损伤。