帕尔卡尼醇和依那普利对动脉粥样硬化患者肾脏炎症/氧化应激的影响。

Kazim Husain, Edu Suarez, Angel Isidro, Wilfredo Hernandez, Leon Ferder
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引用次数: 12

摘要

目的:探讨派卡尔醇和依那普利对apoe敲除小鼠肾脏炎症和氧化应激的保护作用。方法:动物治疗4个月,分为(1)apoe敲除加载药组、(2)apoe敲除加依那普利组(200 ng,每周3次)、(3)apoe敲除加依那普利组(30 mg/L)、(4)apoe敲除加依那普利组和(5)正常组。用尾袖带法记录血压。用分光光度计和Western blot分析分离肾脏进行生化分析。结果:apoe缺陷小鼠出现血压升高(127±3 mmHg),依那普利和依那普利加帕利西醇治疗可改善血压升高,但帕利西醇单独治疗不能改善血压升高。apoe敲除小鼠肾脏丙二醛浓度、p22(phox)、锰-超氧化物歧化酶、诱导型一氧化氮合酶(NOS)、单核细胞化学引诱蛋白-1、肿瘤坏死因子- α和转化生长因子-β1水平显著升高,而还原性谷胱甘肽、CuZn-SOD和eNOS水平显著降低。特立醇、依那普利联合用药可改善apoe敲除动物的肾脏炎症和氧化应激。结论:帕里西醇和依那普利联合治疗可改善动脉粥样硬化动物的肾脏炎症和氧化应激。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Effect of paricalcitol and enalapril on renal inflammation/oxidative stress in atherosclerosis.

Aim: To investigate the protective effect of paricalcitol and enalapril on renal inflammation and oxidative stress in ApoE-knock out mice.

Methods: Animals treated for 4 mo as group (1) ApoE-knock out plus vehicle, group (2) ApoE-knock out plus paricalcitol (200 ng thrice a week), (3) ApoE-knock out plus enalapril (30 mg/L), (4) ApoE-knock out plus paricalcitol plus enalapril and (5) normal. Blood pressure (BP) was recorded using tail cuff method. The kidneys were isolated for biochemical assays using spectrophotometer and Western blot analyses.

Results: ApoE-deficient mice developed high BP (127 ± 3 mmHg) and it was ameliorated by enalapril and enalapril plus paricalcitol treatments but not with paricalcitol alone. Renal malondialdehyde concentrations, p22(phox), manganese-superoxide dismutase, inducible nitric oxide synthase (NOS), monocyte chemoattractant protein-1, tumor necrosis factor-alpha and transforming growth factor-β1 levels significantly elevated but reduced glutathione, CuZn-SOD and eNOS levels significantly depleted in ApoE-knock out animals compared to normal. Administration of paricalcitol, enalapril and combined together ameliorated the renal inflammation and oxidative stress in ApoE-knock out animals.

Conclusion: Paricalcitol and enalapril combo treatment ameliorates renal inflammation as well as oxidative stress in atherosclerotic animals.

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