Takhtfooladi Mohammad Ashrafzadeh, Jahanshahi Amirali, Jahanshahi Gholamreza, Sotoudeh Amir, Takhtfooladi Hamed Ashrafzadeh, Khansari Mohammadreza
Department of Surgery, Faculty of Specialized Veterinary Sciences, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Acta Cir Bras. 2012 Sep;27(9):611-5. doi: 10.1590/s0102-86502012000900004.
To investigate whether N-acetylcysteine has a protective effect against renal injury as a remote organ after skeletal muscle ischemia-reperfusion in rats.
Twenty Wistar male rats were divided randomly into two experimental groups: group ischemia-reperfusion (group I) and group ischemia-reperfusion + N-acetylcysteine (group II). After ketamine and xylazine anesthesia, femoral artery was exposed. All animals were undergone 2h of ischemia by occlusion femoral artery and 24h of reperfusion. Rats that were treated with N-acetylcysteine given IV at a dose of 150 mg/kg(-1), immediately before reperfusion. After 24h of reperfusion, the blood samples were collected and submitted for evaluation of plasmatic urea, creatinine values and then rats were euthanized and left kidney harvested for histopathological analysis under light microscopy.
The urea (35±7.84 mg.dL(-1)), creatinine (1.46±0.47 mg.dL(-1)) values were significantly lower in group II (P=0.000). Renal histopathologic study in group I showed extensive distal and proximal tubular cells necrosis and sloughing of epithelial cells into the tubular lumen, cast formation in tubule and glomerul, glomerul fibrosis and hemorrhage. Histopathologically, there was a significant difference (p=0.037) between two groups.
The N-acetylcysteine was able to decrease renal injury induced by skeletal muscle ischemia reperfusion in rats.
研究N-乙酰半胱氨酸对大鼠骨骼肌缺血再灌注后作为远隔器官的肾脏损伤是否具有保护作用。
将20只雄性Wistar大鼠随机分为两个实验组:缺血再灌注组(I组)和缺血再灌注+N-乙酰半胱氨酸组(II组)。在氯胺酮和赛拉嗪麻醉后,暴露股动脉。所有动物均经历股动脉闭塞2小时的缺血和24小时的再灌注。在再灌注前立即以150mg/kg(-1)的剂量静脉注射N-乙酰半胱氨酸对大鼠进行治疗。再灌注24小时后,采集血样并送检以评估血浆尿素、肌酐值,然后对大鼠实施安乐死并摘取左肾进行光学显微镜下的组织病理学分析。
II组的尿素(35±7.84mg.dL(-1))、肌酐(1.46±0.47mg.dL(-1))值显著较低(P=0.000)。I组的肾脏组织病理学研究显示广泛的远端和近端肾小管细胞坏死,上皮细胞脱落至肾小管腔内,肾小管和肾小球内形成管型,肾小球纤维化和出血。组织病理学上,两组之间存在显著差异(p=0.037)。
N-乙酰半胱氨酸能够减轻大鼠骨骼肌缺血再灌注诱导的肾损伤。