Van den Branden Christiane, Deman An, Ceyssens Bart, Pauwels Marina, Empsen Christophe, Verbeelen Dierik
Department of Human Anatomy, Vrije Universiteit Brussel, Belgium.
Nephron. 2002 May;91(1):129-33. doi: 10.1159/000057614.
BACKGROUND/AIMS: In the rat Adriamycin model of chronic renal failure, the development of glomerulosclerosis and tubulointerstitial lesions is accompanied by decreased activities and mRNA levels of the antioxidant enzymes. In this study, we investigated the effect of oral vitamin E supplementation on antioxidant enzyme activities in both the cortex and isolated glomeruli from Adriamycin-treated rats.
Glomerulosclerosis, tubulointerstitial lesions and ferric iron deposits were evaluated by histochemical staining methods, and antioxidant enzyme activities were measured by spectrophotometry.
Vitamin E supplementation of the normal diet attenuates Adriamycin-induced glomerulosclerosis and tubulointerstitial lesions, but not proteinuria and serum total cholesterol, low-density lipoprotein cholesterol, triglycerides and total protein concentrations. In the cortex, vitamin E completely prevented a decrease in enzyme activity for Cu/Zn superoxide dismutase and catalase, and partly for Mn superoxide dismutase and glutathione peroxidase. In the glomeruli, vitamin E completely prevented a decrease in activity for Cu/Zn superoxide dismutase, catalase and glutathione peroxidase, and partly for Mn superoxide dismutase.
Dietary supplementation of vitamin E protects the activities of antioxidant enzymes in the kidney cortex and glomeruli, and attenuates the evolution towards terminal renal failure in rats treated with Adriamycin.
背景/目的:在大鼠阿霉素慢性肾衰竭模型中,肾小球硬化和肾小管间质病变的发展伴随着抗氧化酶活性及mRNA水平的降低。在本研究中,我们调查了口服补充维生素E对阿霉素处理大鼠的肾皮质和分离肾小球中抗氧化酶活性的影响。
通过组织化学染色方法评估肾小球硬化、肾小管间质病变和三价铁沉积,并采用分光光度法测量抗氧化酶活性。
在正常饮食中补充维生素E可减轻阿霉素诱导的肾小球硬化和肾小管间质病变,但对蛋白尿、血清总胆固醇、低密度脂蛋白胆固醇、甘油三酯和总蛋白浓度无影响。在肾皮质中,维生素E完全阻止了铜/锌超氧化物歧化酶和过氧化氢酶的活性降低,部分阻止了锰超氧化物歧化酶和谷胱甘肽过氧化物酶的活性降低。在肾小球中,维生素E完全阻止了铜/锌超氧化物歧化酶、过氧化氢酶和谷胱甘肽过氧化物酶的活性降低,部分阻止了锰超氧化物歧化酶的活性降低。
饮食中补充维生素E可保护肾皮质和肾小球中抗氧化酶的活性,并减轻阿霉素处理大鼠向终末期肾衰竭的进展。