Husain Kazim, Ferder Leon, Mizobuchi Masahide, Finch Jane, Slatopolsky Eduardo
Department of Physiology, Pharmacology and Toxicology, Ponce School of Medicine, Ponce, PR 00732, USA.
Am J Nephrol. 2009;29(5):465-72. doi: 10.1159/000178251. Epub 2008 Nov 26.
This study investigated the protective effect of the angiotensin-converting enzyme inhibitor, enalapril, and the vitamin D analog, paricalcitol, alone or in combination, on cardiac oxidative stress in uremic rats.
Rats were made uremic by 5/6 nephrectomy and treated for 4 months as follows: (1) uremic + vehicle (n = 11); (2) uremic + enalapril (30 mg/l in drinking water, n = 13); (3) uremic + paricalcitol (200 ng 3x week, n = 6); (4) uremic + enalapril + paricalcitol (n = 14), and (5) controls (n = 6).
Cardiac NADPH oxidase activity increased by 300% in uremic rats compared to normal controls. Treatment with enalapril, paricalcitol or the combination of the two protected uremic rats from cardiac oxidative stress by inhibiting enzyme activity. Cardiac malondialdehyde (MDA) levels were significantly increased in uremic rats compared to normal controls. Only the combination therapy inhibited the increase in MDA levels in uremic rats. Cardiac glutathione was significantly reduced in uremic rats compared to normal controls. Enalapril, paricalcitol or the two in combination all protected against this reduction in glutathione. Cardiac copper/zinc superoxide dismutase (CuZn-SOD) activity decreased whereas manganese (Mn-SOD) activity increased in uremic rats compared to controls. Both mono and combination therapies ameliorated the alterations in cardiac SOD activity seen in uremic rats.
Enalapril, paricalcitol and their combined therapy afford protection against cardiac oxidative stress in uremia.
本研究调查了血管紧张素转换酶抑制剂依那普利和维生素D类似物帕立骨化醇单独或联合使用对尿毒症大鼠心脏氧化应激的保护作用。
通过5/6肾切除术使大鼠患尿毒症,并按以下方式治疗4个月:(1)尿毒症+赋形剂(n = 11);(2)尿毒症+依那普利(饮用水中30 mg/l,n = 13);(3)尿毒症+帕立骨化醇(每周3次,每次200 ng,n = 6);(4)尿毒症+依那普利+帕立骨化醇(n = 14),以及(5)对照组(n = 6)。
与正常对照组相比,尿毒症大鼠心脏NADPH氧化酶活性增加了300%。依那普利、帕立骨化醇或两者联合治疗通过抑制酶活性保护尿毒症大鼠免受心脏氧化应激。与正常对照组相比,尿毒症大鼠心脏丙二醛(MDA)水平显著升高。只有联合治疗抑制了尿毒症大鼠MDA水平的升高。与正常对照组相比,尿毒症大鼠心脏谷胱甘肽显著降低。依那普利、帕立骨化醇或两者联合使用均能防止谷胱甘肽的这种降低。与对照组相比,尿毒症大鼠心脏铜/锌超氧化物歧化酶(CuZn-SOD)活性降低,而锰超氧化物歧化酶(Mn-SOD)活性增加。单一疗法和联合疗法均改善了尿毒症大鼠心脏SOD活性的改变。
依那普利、帕立骨化醇及其联合治疗可保护尿毒症患者免受心脏氧化应激。