Lee H S, Jeong J Y, Kim B C, Kim Y S, Zhang Y Z, Chung H K
Department of Pathology, Seoul National University College of Medicine, Korea.
Kidney Int. 1997 Apr;51(4):1151-9. doi: 10.1038/ki.1997.158.
Lipid peroxidation may be involved in the pathogenesis of focal segmental glomerulosclerosis (FSGS). In the present study we examined whether lipid-soluble antioxidants, probucol and vitamin E, could inhibit renal injury in rats with chronic puromycin aminonucleoside (PA) nephrosis and dietary hypercholesterolemia by protecting lipoproteins from oxidation. Male Sprague-Dawley rats received six intraperitoneal injections of PA over a 10 week period and were fed a high cholesterol (HC) diet (PA-HC) or the same diet supplemented with either 1% probucol or vitamin E (100 IU/kg) for 32 weeks. For comparison, a group of rats received PA injections and a normal diet (PA-normal) with or without probucol or vitamin E. Another group rats received saline injections instead of PA and were fed a HC diet (Sal-HC) with or without probucol or vitamin E. At the end of the experiment, proteinuria, FSGS and tubulointerstitial lesions were present in the untreated rats with PA-HC or PA-normal. The magnitude of these lesions was significantly greater in the PA-HC rats than the PA-normal. In contrast to the PA-HC group with hypercholesterolemia, the PA-normal group did not show hypercholesterolemia from week 16 onwards. The rats with PA-HC alone showed significantly higher renal cortical malondialdehyde (MDA) levels and greater susceptibility of plasma very low density lipoprotein (VLDL) + low density lipoprotein (LDL) to the copper-mediated oxidation than the rats with PA-normal or Sal-HC alone. The administration of probucol or vitamin E in the rats with PA-HC significantly reduced the susceptibility of plasma VLDL + LDL to in vitro oxidation, renal cortical MDA level, proteinuria, mesangial volume density and magnitude of FSGS and interstitial lesions. Immunohistochemical staining of renal tissue showed focal segmental distribution of oxidized LDL (Ox-LDL) in the glomeruli of rats with PA-HC. Administration of probucol or vitamin E reduced the intensity of Ox-LDL staining. The staining with ED1 demonstrated that infiltrating glomerular macrophages were significantly more prevalent in the untreated rats with PA-HC than PA-normal or Sal-HC. Treatment with probucol or vitamin E significantly reduced the number of glomerular macrophages in the rats with PA-HC. These results suggest that alimentary hypercholesterolemia aggravates the renal damage in association with increased renal lipid peroxides in chronic PA nephrosis, and that dietary probucol or vitamin E attenuates renal injury in rats with PA-HC possibly by making lipoproteins resistant to oxidation and by inhibiting intraglomerular macrophage infiltration.
脂质过氧化可能参与局灶节段性肾小球硬化(FSGS)的发病机制。在本研究中,我们检测了脂溶性抗氧化剂普罗布考和维生素E是否可通过保护脂蛋白免受氧化,从而抑制慢性嘌呤霉素氨基核苷(PA)肾病和饮食性高胆固醇血症大鼠的肾损伤。雄性Sprague-Dawley大鼠在10周内接受6次PA腹腔注射,并给予高胆固醇(HC)饮食(PA-HC)或添加1%普罗布考或维生素E(100 IU/kg)的相同饮食,持续32周。为作比较,一组大鼠接受PA注射并给予正常饮食(PA-正常),同时添加或不添加普罗布考或维生素E。另一组大鼠接受生理盐水注射而非PA,并给予HC饮食(生理盐水-HC),同时添加或不添加普罗布考或维生素E。实验结束时,未治疗的PA-HC或PA-正常大鼠出现蛋白尿、FSGS和肾小管间质病变。PA-HC大鼠这些病变的严重程度显著高于PA-正常大鼠。与伴有高胆固醇血症的PA-HC组不同,PA-正常组从第16周起未出现高胆固醇血症。单独给予PA-HC的大鼠肾皮质丙二醛(MDA)水平显著更高,血浆极低密度脂蛋白(VLDL)+低密度脂蛋白(LDL)对铜介导氧化的敏感性也高于单独给予PA-正常或生理盐水-HC的大鼠。在PA-HC大鼠中给予普罗布考或维生素E可显著降低血浆VLDL + LDL对体外氧化的敏感性、肾皮质MDA水平、蛋白尿、系膜体积密度以及FSGS和间质病变的严重程度。肾组织免疫组化染色显示,PA-HC大鼠肾小球中氧化型LDL(Ox-LDL)呈局灶节段性分布。给予普罗布考或维生素E可降低Ox-LDL染色强度。ED1染色显示,未治疗的PA-HC大鼠肾小球内浸润的巨噬细胞显著多于PA-正常或生理盐水-HC大鼠。用普罗布考或维生素E治疗可显著减少PA-HC大鼠肾小球巨噬细胞数量。这些结果表明,饮食性高胆固醇血症与慢性PA肾病中肾脂质过氧化物增加相关,会加重肾损伤,而饮食中的普罗布考或维生素E可能通过使脂蛋白抗氧化以及抑制肾小球内巨噬细胞浸润来减轻PA-HC大鼠的肾损伤。